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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/08/13 22:27:36」(JST)

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For other uses, see Leaf (disambiguation).

Leaf of Tilia tomentosa (Silver lime tree)

A leaf is an organ of a vascular plant and is the principal lateral appendage of the stem. The leaves and stem together form the shoot. Foliage is a mass noun that refers to leaves collectively.

Diagram of a simple leaf.

1. Apex
2. Midvein (Primary vein)
3. Secondary vein.
4. Lamina.
5. Leaf margin
6. Petiole
7. Bud
8. Stem

Typically a leaf is a thin, dorsiventrally flattened organ, borne above ground and specialized for photosynthesis. In most leaves, the primary photosynthetic tissue, the (palisade mesophyll), is located on the upper side of the blade or lamina of the leaf but in some species, including the mature foliage of Eucalyptus palisade mesophyll is present on both sides and the leaves are said to be isobilateral. Most leaves have distinctive upper (adaxial) and lower (abaxial) surfaces that differ in colour, hairiness, the number of stomata (pores that intake and output gases), epicuticular wax amount and structure and other features.

Broad, flat leaves with complex venation are known as megaphylls and the species that bear them, the majority, as broad-leaved or megaphyllous plants. In others, such as the clubmosses, with different evolutionary origins, the leaves are simple, with only a single vein and are known as microphylls.

Some leaves, such as bulb scales are not above ground, and in many aquatic species the leaves are submerged in water. Succulent plants often have thick juicy leaves, but some leaves are without major photosynthetic function and may be dead at maturity, as in some cataphylls, and spines). Furthermore, several kinds of leaf-like structures found in vascular plants are not totally homologous with them. Examples include flattened plant stems called phylloclades and cladodes, and flattened leaf stems called phyllodes which differ from leaves both in their structure and origin. Many structures of non-vascular plants, such as the phyllids of mosses and liverworts and even of some foliose lichens, which are not plants at all (in the sense of being members of the kingdom Plantae), look and function much like leaves.

General characteristics

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3D rendering of a computed tomography scan of a leaf

Typically leaves are broad, flat and thin (dorsiventrally flattened), at least in their early development, thereby maximising the surface area directly exposed to light and enabling the light to penetrate the tissues and reach the chloroplasts, thus promoting photosynthesis. They are arranged on the plant so as to expose their surfaces to light as efficiently as possible without shading each other, but there are many exceptions and complications. For instance plants adapted to windy conditions may have pendent leaves, such as in many willows and eucalypts. Also conifers, whose leaves are needle shaped. The flat, or laminar, shape also maximises thermal contact with the surrounding air. The leaf shape also minimises damage from wind, by creating turbulence rather than resistance. Functionally, in addition to photosynthesis the leaf is the principal site of transpiration and guttation. Leaves also function to store chemical energy and water (especially succulents) and may become specialised organs serving other functions.

The internal organisation of most kinds of leaves has evolved to maximise exposure of the photosynthetic organelles, the chloroplasts, to light and to increase the absorption of carbon dioxide. Their surfaces are waterproofed by the plant cuticle and gas exchange between the mesophyll cells and the atmosphere is controlled by minute openings called stomata, about 10 μm which open or close to regulate the rate exchange of carbon dioxide, oxygen, and water vapour into and out of the internal intercellular space system. Stomatal opening is controlled by the turgor pressure in a pair of guard cells that surround the stomatal aperture. In any square centimeter of a plant leaf there may be from 1,000 to 100,000 stomata.

Many gymnosperms have thin needle-like or scale-like leaves that can be advantageous in cold climates with frequent snow and frost. These are interpreted as reduced from megaphyllous leaves of their Devonian ancestors. Some leaf forms are adapted to modulate the amount of light they absorb to avoid or mitigate excessive heat, ultraviolet damage, or desiccation, or to sacrifice light-absorption efficiency in favour of protection from herbivory. For xerophytes the major constraint is not light flux or intensity, but drought. Some window plants such as Fenestraria species and some Haworthia species such as Haworthia tesselata and Haworthia truncata are examples of xerophytes. and Bulbine mesembryanthemoides.

Near the ground these Eucalyptus saplings have juvenile dorsiventral foliage from the previous year, but this season their newly sprouting foliage is isobilateral, like the mature foliage on the adult trees above

The shape and structure of leaves vary considerably from species to species of plant, depending largely on their adaptation to climate and available light, but also to other factors such as grazing animals (such as deer), available nutrients, and ecological competition from other plants. Considerable changes in leaf type occur within species too, for example as a plant matures; as a case in point Eucalyptus species commonly have isobilateral, pendent leaves when mature and dominating their neighbours; however, such trees tend to have erect or horizontal dorsiventral leaves as seedlings, when their growth is limited by the available light. Other factors include the need to balance water loss at high temperature and low humidity against the need to absorb atmospheric carbon dioxide. In most plants leaves also are the primary organs responsible for transpiration and guttation (beads of fluid forming at leaf margins).

Leaves can also store food and water, and are modified accordingly to meet these functions, for example in the leaves of succulent plants and in bulb scales. The concentration of photosynthetic structures in leaves requires that they be richer in protein, minerals, and sugars than, say, woody stem tissues. Accordingly, leaves are prominent in the diet of many animals.

A leaf shed in autumn.

Correspondingly, leaves represent heavy investment on the part of the plants bearing them, and their retention or disposition are the subject of elaborate strategies for dealing with pest pressures, seasonal conditions, and protective measures such as the growth of thorns and the production of phytoliths, lignins, tannins and poisons.

Deciduous plants in frigid or cold temperate regions typically shed their leaves in autumn, whereas in areas with a severe dry season, some plants may shed their leaves until the dry season ends. In either case the shed leaves may be expected to contribute their retained nutrients to the soil where they fall.

In contrast, many other non-seasonal plants, such as palms and conifers, retain their leaves for long periods; Welwitschia retains its two main leaves throughout a lifetime that may exceed a thousand years.

The leaf-like organs of Bryophytes (e.g., mosses and liverworts), known as phyllids, differ morphologically from the leaves of vascular plants in that they lack vascular tissue, are usually only a single cell thick and have no cuticle stomata or internal system of intercellular spaces.

Simple, vascularised leaves (microphylls) first evolved as enations, extensions of the stem, in clubmosses such as Baragwanathia during the Silurian period. True leaves or euphylls of larger size and with more complex venation did not become widespread in other groups until the Devonian period, by which time the carbon dioxide concentration in the atmosphere had dropped significantly. This occurred independently in several separate lineages of vascular plants, in progymnosperms like Archaeopteris, in Sphenopsida, ferns and later in the gymnosperms and angiosperms. Euphylls are also referred to as macrophylls or megaphylls (large leaves).

Morphology (large-scale features)

A structurally complete leaf of an angiosperm consists of a petiole (leaf stalk), a lamina (leaf blade), and stipules (small structures located to either side of the base of the petiole). Not every species produces leaves with all of these structural components. In certain species, paired stipules are not obvious or are absent altogether. A petiole may be absent, or the blade may not be laminar (flattened). The tremendous variety shown in leaf structure (anatomy) from species to species is presented in detail below under morphology. The petiole mechanically links the leaf to the plant and provides the route for transfer of water and sugars to and from the leaf. The lamina is typically the location of the majority of photosynthesis. The upper (adaxial) angle between a leaf and a stem is known as the axil of the leaf. It is often the location of a bud. Structures located there are called "axillary".

Translucent glands in Citrus leaves

External leaf characteristics, such as shape, margin, hairs, the petiole, and the presence of stipules, are important for identifying plant species, and botanists have developed a rich terminology for describing leaf characteristics. Leaves have determinate growth. They grow to a specific pattern and shape and then stop. Other plant parts like stems or roots have non-determinate growth, and will usually continue to grow as long as they have the resources to do so.

The type of leaf is usually characteristic of a species (monomorphic), although some species produce more than one type of leaf (dimorphic or polymorphic). The longest leaves are those of the Raffia palm, R. regalis which may be up to 25 m (82 ft) long and 3 m (9.8 ft) wide. The terminology associated with the description of leaf morphology is presented, in illustrated form, at Wikibooks.

Prostrate leaves in Crossyne guttata

Where leaves are basal, and lie on the ground, they are referred to as prostrate.

Basic leaf types

Leaves of the White Spruce (Picea glauca) are needle-shaped and their arrangement is spiral

• Ferns have fronds
• Conifer leaves are typically needle- or awl-shaped or scale-like
• Angiosperm (flowering plant) leaves: the standard form includes stipules, a petiole, and a lamina
• Lycophytes have microphyll leaves.
• Sheath leaves (type found in most grasses and many other monocots)
• Other specialized leaves (such as those of Nepenthes, a pitcher plant)

Arrangement on the stem

Main article: Phyllotaxis

Different terms are usually used to describe the arrangement of leaves on the stem (phyllotaxis):

The leaves on this plant are arranged in pairs opposite one another, with successive pairs at right angles to each other (decussate) along the red stem. Note the developing buds in the axils of these leaves.

Alternate

Leaf attachments are singular at nodes, and leaves alternate direction, to a greater or lesser degree, along the stem.

Basal

Arising from the base of the stem.

Cauline

Arising from the aerial stem.

Opposite

Two structures, one on each opposite side of the stem, typically leaves, branches, or flower parts. Leaf attachments are paired at each node and decussate if, as typical, each successive pair is rotated 90° progressing along the stem.

Whorled, or verticillate

Three or more leaves attach at each point or node on the stem. As with opposite leaves, successive whorls may or may not be decussate, rotated by half the angle between the leaves in the whorl (i.e., successive whorls of three rotated 60°, whorls of four rotated 45°, etc.). Opposite leaves may appear whorled near the tip of the stem. Pseudoverticillate describes an arrangement only appearing whorled, but not actually so.

Rosulate

Leaves form a rosette.

Rows

The term, distichous, literally means two rows. Leaves in this arrangement may be alternate or opposite in their attachment. The term, 2-ranked, is equivalent. The terms, tristichous and tetrastichous, are sometimes encountered. For example, the "leaves" (actually microphylls) of most species of Selaginella are tetrastichous, but not decussate.

As a stem grows, leaves tend to appear arranged around the stem in a way that optimizes yield of light. In essence, leaves form a helix pattern centered around the stem, either clockwise or counterclockwise, with (depending upon the species) the same angle of divergence. There is a regularity in these angles and they follow the numbers in a Fibonacci sequence: 1/2, 2/3, 3/5, 5/8, 8/13, 13/21, 21/34, 34/55, 55/89. This series tends to the golden angle, which is approximately 360° × 34/89 ≈ 137.52° ≈ 137° 30′. In the series, the numerator indicates the number of complete turns or "gyres" until a leaf arrives at the initial position and the denominator indicates the number of leaves in the arrangement. This can be demonstrated by the following:

• Alternate leaves have an angle of 180° (or 1/2)
• 120° (or 1/3): 3 leaves in 1 circle
• 144° (or 2/5): 5 leaves in 2 gyres
• 135° (or 3/8): 8 leaves in 3 gyres.

Divisions of the blade

A leaf with laminar structure and pinnate venation

Two basic forms of leaves can be described considering the way the blade (lamina) is divided. A simple leaf has an undivided blade. However, the leaf shape may be formed of lobes, but the gaps between lobes do not reach to the main vein. A compound leaf has a fully subdivided blade, each leaflet of the blade being separated along a main or secondary vein. Because each leaflet can appear to be a simple leaf, it is important to recognize where the petiole occurs to identify a compound leaf. Compound leaves are a characteristic of some families of higher plants, such as the Fabaceae. The middle vein of a compound leaf or a frond, when it is present, is called a rachis.

Palmately compound

Leaves have the leaflets radiating from the end of the petiole, like fingers of the palm of a hand; e.g., Cannabis (hemp) and Aesculus (buckeyes).

Pinnately compound

Leaves have the leaflets arranged along the main or mid-vein.

Odd pinnate

With a terminal leaflet; e.g., Fraxinus (ash).

Even pinnate

lacking a terminal leaflet; e.g., Swietenia (mahogany).

Bipinnately compound

Leaves are twice divided: the leaflets are arranged along a secondary vein that is one of several branching off the rachis. Each leaflet is called a "pinnule". The group of pinnules on each secondary vein forms a "pinna"; e.g., Albizia (silk tree).

Trifoliate (or trifoliolate)

A pinnate leaf with just three leaflets; e.g., Trifolium (clover), Laburnum (laburnum).

Pinnatifid

Pinnately dissected to the central vein, but with the leaflets not entirely separate; e.g., Polypodium, some Sorbus (whitebeams). In pinnately veined leaves the central vein in known as the midrib.

Characteristics of the petiole

The overgrown petioles of rhubarb (Rheum rhabarbarum) are edible.

Petiolated leaves have a petiole (leaf stem), and are said to be petiolate.

Sessile (epetiolate) leaves have no petiole and the blade attaches directly to the stem. Subpetiolate leaves are nearly petiolate or have an extremely short petiole and may appear to be sessile.

In clasping or decurrent leaves, the blade partially surrounds the stem.

When the leaf base completely surrounds the stem, the leaves are said to be perfoliate, such as in Claytonia perfoliata.

In peltate leaves, the petiole attaches to the blade inside the blade margin.

In some Acacia species, such as the koa tree (Acacia koa), the petioles are expanded or broadened and function like leaf blades; these are called phyllodes. There may or may not be normal pinnate leaves at the tip of the phyllode.

A stipule, present on the leaves of many dicotyledons, is an appendage on each side at the base of the petiole, resembling a small leaf. Stipules may be lasting and not be shed (a stipulate leaf, such as in roses and beans), or be shed as the leaf expands, leaving a stipule scar on the twig (an exstipulate leaf). The situation, arrangement, and structure of the stipules is called the "stipulation".

Free, lateral

As in Hibiscus.

Adnate

Fused to the petiole base, as in Rosa.

Ochreate

Provided with ochrea, or sheath-formed stipules, as in Polygonaceae; e.g., rhubarb.

Encircling the petiole base

Interpetiolar

Between the petioles of two opposite leaves, as in Rubiaceae.

Intrapetiolar

Between the petiole and the subtending stem, as in Malpighiaceae.

Venation

Branching veins on underside of taro leaf

The venation within the bract of a lime tree.

There are two subtypes of venation, namely, craspedodromous, where the major veins stretch up to the margin of the leaf, and camptodromous, when major veins extend close to the margin, but bend before they intersect with the margin.

Feather-veined, reticulate (also called pinnate-netted, penniribbed, penninerved, or penniveined)

The veins arise pinnately from a single mid-vein and subdivide into veinlets. These, in turn, form a complicated network. This type of venation is typical for (but by no means limited to) dicotyledons.

Plinervy

Three main veins branch at the base of the lamina and run essentially parallel subsequently, as in Ceanothus and in Celtis. A similar pattern (with 3-7 veins) is especially conspicuous in Melastomataceae.

Palmate-netted, palmate-veined, fan-veined

Several main veins diverge from near the leaf base where the petiole attaches, and radiate toward the edge of the leaf; e.g., most Acer (maples).

Parallel-veined, parallel-ribbed, parallel-nerved, penniparallel

Veins run parallel for the length of the leaf, from the base to the apex. Commissural veins (small veins) connect the major parallel veins. Typical for most monocotyledons, such as grasses.

Dichotomous

There are no dominant bundles, with the veins forking regularly by pairs; found in Ginkgo and some pteridophytes.

Micrograph of a leaf skeleton

Although it is the more complex pattern, branching veins appear to be plesiomorphic and in some form were present in ancient seed plants as long as 250 million years ago. A pseudo-reticulate venation that is actually a highly modified penniparallel one is an autapomorphy of some Melanthiaceae, which are monocots; e.g., Paris quadrifolia (True-lover's Knot).

Morphology changes within a single plant

Homoblasty

Characteristic in which a plant has small changes in leaf size, shape, and growth habit between juvenile and adult stages.

Heteroblasty

Characteristic in which a plant has marked changes in leaf size, shape, and growth habit between juvenile and adult stages.

Terminology

Leaf morphology terms

Shape

Main article: Glossary of leaf shapes

Leaves showing various morphologies. Clockwise from upper left: tripartite lobation, elliptic with serrulate margin, palmate venation, acuminate odd-pinnate (center), pinnatisect, lobed, elliptic with entire margin

Edge (margin)

Image	Term	Latin	Description
	Entire	Forma integra	Even; with a smooth margin; without toothing
	Ciliate	Ciliata	Fringed with hairs
	Crenate	Crenata	Wavy-toothed; dentate with rounded teeth
	Dentate	Dentata	Toothed May be coarsely dentate, having large teeth or glandular dentate, having teeth which bear glands
	Denticulate	Denticulata	Finely toothed
	Doublely serate	Duplicato-dentata	Each tooth bearing smaller teeth
	Serrate	Serrata	Saw-toothed; with asymmetrical teeth pointing forward
	Serrulate	Serrulata	Finely serrate
	Sinuate	Sinuosa	With deep, wave-like indentations; coarsely crenate
	Lobate	Lobata	Indented, with the indentations not reaching the center
	Undulate	Undulata	With a wavy edge, shallower than sinuate
	Spiny or pungent	Spiculata	With stiff, sharp points such as thistles

Tip

Acuminate

Long-pointed, prolonged into a narrow, tapering point in a concave manner.

Acute

Ending in a sharp, but not prolonged point

Cuspidate

With a sharp, elongated, rigid tip; tipped with a cusp.

Emarginate

Indented, with a shallow notch at the tip.

Mucronate

Abruptly tipped with a small short point, as a continuation of the midrib; tipped with a mucro.

Mucronulate

Mucronate, but with a noticeably diminutive spine, a mucronule.

Obcordate

Inversely heart-shaped, deeply notched at the top.

Obtuse

Rounded or blunt

Truncate

Ending abruptly with a flat end, that looks cut off.

Haworthia truncata, a classic example of truncate leaves

Base

Acuminate

Coming to a sharp, narrow, prolonged point.

Acute

Coming to a sharp, but not prolonged point.

Auriculate

Ear-shaped.

Cordate

Heart-shaped with the notch towards the stalk.

Cuneate

Wedge-shaped.

Hastate

Shaped like an halberd and with the basal lobes pointing outward.

Oblique

Slanting.

Reniform

Kidney-shaped but rounder and broader than long.

Rounded

Curving shape.

Sagittate

Shaped like an arrowhead and with the acute basal lobes pointing downward.

Truncate

Ending abruptly with a flat end, that looks cut off.

Surface

Scale-shaped leaves of a Norfolk Island Pine, Araucaria heterophylla.

Coriaceous

Leathery; stiff and tough, but somewhat flexible.

Farinose

Bearing farina; mealy, covered with a waxy, whitish powder.

Glabrous

Smooth, not hairy.

Glaucous

With a whitish bloom; covered with a very fine, bluish-white powder.

Glutinous

Sticky, viscid.

Lepidote

Coated with small scales (thus elepidote, without such scales).

Maculate

Stained, spotted, compare immaculate.

Papillate, or papillose

Bearing papillae (minute, nipple-shaped protuberances).

Pubescent

Covered with erect hairs (especially soft and short ones).

Punctate

Marked with dots; dotted with depressions or with translucent glands or colored dots.

Rugose

Deeply wrinkled; with veins clearly visible.

Scurfy

Covered with tiny, broad scalelike particles.

Tuberculate

Covered with tubercles; covered with warty prominences.

Verrucose

Warted, with warty outgrowths.

Viscid, or viscous

Covered with thick, sticky secretions.

The leaf surface is also host to a large variety of microorganisms; in this context it is referred to as the phyllosphere.

The parallel veins within an iris leaf

Hairiness

Common mullein (Verbascum thapsus) leaves are covered in dense, stellate trichomes.

Scanning electron microscope image of trichomes on the lower surface of a Coleus blumei (coleus) leaf

"Hairs" on plants are properly called trichomes. Leaves can show several degrees of hairiness. The meaning of several of the following terms can overlap.

Arachnoid, or arachnose

With many fine, entangled hairs giving a cobwebby appearance.

Barbellate

With finely barbed hairs (barbellae).

Bearded

With long, stiff hairs.

Bristly

With stiff hair-like prickles.

Canescent

Hoary with dense grayish-white pubescence.

Ciliate

Marginally fringed with short hairs (cilia).

Ciliolate

Minutely ciliate.

Floccose

With flocks of soft, woolly hairs, which tend to rub off.

Glabrescent

Losing hairs with age.

Glabrous

No hairs of any kind present.

Glandular

With a gland at the tip of the hair.

Hirsute

With rather rough or stiff hairs.

Hispid

With rigid, bristly hairs.

Hispidulous

Minutely hispid.

Hoary

With a fine, close grayish-white pubescence.

Lanate, or lanose

With woolly hairs.

Pilose

With soft, clearly separated hairs.

Puberulent, or puberulous

With fine, minute hairs.

Pubescent

With soft, short and erect hairs.

Scabrous, or scabrid

Rough to the touch.

Sericeous

Silky appearance through fine, straight and appressed (lying close and flat) hairs.

Silky

With adpressed, soft and straight pubescence.

Stellate, or stelliform

With star-shaped hairs.

Strigose

With appressed, sharp, straight and stiff hairs.

Tomentose

Densely pubescent with matted, soft white woolly hairs.

Cano-tomentose

Between canescent and tomentose.

Felted-tomentose

Woolly and matted with curly hairs.

Tomentulose

Minutely or only slightly tomentose.

Villous

With long and soft hairs, usually curved.

Woolly

With long, soft and tortuous or matted hairs.

Timing

Hysteranthous (hysteranthy)

Developing after the flowers

Synanthous (synanthy)

Developing at the same time as the flowers

Vein patterning

Channelled

Sunken below the surface, resulting in a rounded channel

Image	Term	Description
	Arcuate	Secondary arching toward the apex
	Dichotomous	Veins splitting in two
	Longitudinal	All veins aligned mostly with the midvein
	Palmate	Veins coming from one point like fingers come from the palm of the hand
	Parallel	All veins parallel and not intersecting
	Pinnate	Secondary veins borne from midrib
	Reticulate	All veins branching repeatedly, net veined
	Rotate	Veins coming from the center of the leaf and radiating toward the edges
	Transverse	Nervure tertiaire reliant les nervures secondaires

Size

Main article: Leaf size

The terms megaphyll, macrophyll, mesophyll, notophyll, microphyll, nanophyll and leptophyll are used to describe leaf sizes (in descending order), in a classification devised in 1934 by Christen C. Raunkiær and since modified by others.

Anatomy (medium and small scale)

Medium-scale features

Leaves are normally extensively vascularised and typically have networks of vascular bundles containing xylem, which supplies water for photosynthesis, and phloem, which transports the sugars produced by photosynthesis. Many leaves are covered in trichomes (small hairs) which have diverse structures and functions.

Small-scale features

The major tissue systems present are

1. The epidermis, which covers the upper and lower surfaces
2. The mesophyll tissue inside the leaf, which is rich in chloroplasts (also called chlorenchyma)
3. The arrangement of veins (the vascular tissue)

These three tissue systems typically form a regular organisation at the cellular scale. Specialised cells that differ markedly from surrounding cells, and which often synthesise specialised products such as crystals, are termed idioblasts.

Major leaf tissues

• Cross-section of a leaf

• Epidermal cells

• Spongy mesophyll cells

Epidermis

SEM image of the leaf epidermis of Nicotiana alata, showing trichomes (hair-like appendages) and stomata (eye-shaped slits, visible at full resolution).

The epidermis is the outer layer of cells covering the leaf. It is covered with a waxy cuticle which is impermeable to liquid water and water vapor and forms the boundary separating the plant's inner cells from the external world. The cuticle is in some cases thinner on the lower epidermis than on the upper epidermis, and is generally thicker on leaves from dry climates as compared with those from wet climates. The epidermis serves several functions: protection against water loss by way of transpiration, regulation of gas exchange, secretion of metabolic compounds, and (in some species) absorption of water. Most leaves show dorsoventral anatomy: The upper (adaxial) and lower (abaxial) surfaces have somewhat different construction and may serve different functions.

The epidermis tissue includes several differentiated cell types; epidermal cells, epidermal hair cells (trichomes), cells in the stomatal complex; guard cells and subsidiary cells. The epidermal cells are the most numerous, largest, and least specialized and form the majority of the epidermis. These are typically more elongated in the leaves of monocots than in those of dicots.

Chloroplasts are generally absent in epidermal cells, the exception being the guard cells of the stomata. The stomatal pores perforate the epidermis and are surrounded on each side by chloroplast-containing guard cells, and two to four subsidiary cells that lack chloroplasts, forming a specialized cell group known as the stomatal complex. The opening and closing of the stomatal aperture is controlled by the stomatal complex and regulates the exchange of gases and water vapor between the outside air and the interior of the leaf. Stomata therefore play the important role in allowing photosynthesis without letting the leaf dry out. In a typical leaf, the stomata are more numerous over the abaxial (lower) epidermis than the adaxial (upper) epidermis and are more numerous in plants from cooler climates.

Mesophyll

For the term Mesophyll in the size classification of leaves, see Leaf size.

Most of the interior of the leaf between the upper and lower layers of epidermis is a parenchyma (ground tissue) or chlorenchyma tissue called the mesophyll (Greek for "middle leaf"). This assimilation tissue is the primary location of photosynthesis in the plant. The products of photosynthesis are called "assimilates".

In ferns and most flowering plants, the mesophyll is divided into two layers:

• An upper palisade layer of vertically elongated cells, one to two cells thick, directly beneath the adaxial epidermis, with intercellular air spaces between them. Its cells contain many more chloroplasts than the spongy layer. These long cylindrical cells are regularly arranged in one to five rows. Cylindrical cells, with the chloroplasts close to the walls of the cell, can take optimal advantage of light. The slight separation of the cells provides maximum absorption of carbon dioxide. This separation must be minimal to afford capillary action for water distribution. In order to adapt to their different environment (such as sun or shade), plants had to adapt this structure to obtain optimal result. Sun leaves have a multi-layered palisade layer, while shade leaves or older leaves closer to the soil are single-layered.
• Beneath the palisade layer is the spongy layer. The cells of the spongy layer are more branched and not so tightly packed, so that there are large intercellular air spaces between them for oxygen and carbon dioxide to diffuse in and out of during respiration and photosynthesis. These cells contain fewer chloroplasts than those of the palisade layer. The pores or stomata of the epidermis open into substomatal chambers, which are connected to the air spaces between the spongy layer cells.

Leaves are normally green, due to chlorophyll in chloroplasts in the chlorenchyma cells. Plants that lack chlorophyll cannot photosynthesize.

Veins

The veins of a bramble leaf

The veins are the vascular tissue of the leaf and are located in the spongy layer of the mesophyll. The pattern of the veins is called venation. In angiosperms the venation is typically parallel in monocotyledons and forms an interconnecting network in broad-leaved plants. They were once thought to be typical examples of pattern formation through ramification, but they may instead exemplify a pattern formed in a stress tensor field.

A vein is made up of a vascular bundle. At the core of each bundle are clusters of two distinct types of conducting cells:

• Xylem: cells that bring water and minerals from the roots into the leaf.
• Phloem: cells that usually move sap, with dissolved sucrose, produced by photosynthesis in the leaf, out of the leaf.
• A sheath of ground tissue made of lignin surrounding the vascular tissue. This sheath has a mechanical role in strengthening the rigidity of the leaf.

The xylem typically lies on the adaxial side of the vascular bundle and the phloem typically lies on the abaxial side. Both are embedded in a dense parenchyma tissue, called the sheath, which usually includes some structural collenchyma tissue.

Leaf development

According to Agnes Arber's partial-shoot theory of the leaf, leaves are partial shoots, being derived from leaf primordia of the shoot apex. Compound leaves are closer to shoots than simple leaves. Developmental studies have shown that compound leaves, like shoots, may branch in three dimensions. On the basis of molecular genetics, Eckardt and Baum (2010) concluded that "it is now generally accepted that compound leaves express both leaf and shoot properties."

Adaptations

Poinsettia bracts are leaves which have evolved red pigmentation in order to attract insects and birds to the central flowers, an adaptive function normally served by petals (which are themselves leaves highly modified by evolution).

In the course of evolution, leaves have adapted to different environments in the following ways:

• A certain surface structure avoids moistening by rain and contamination (See Lotus effect).
• Sliced leaves reduce wind resistance.
• Hairs on the leaf surface trap humidity in dry climates and create a boundary layer reducing water loss.
• Waxy leaf surfaces reduce water loss.
• Large surface area provides large area for sunlight and shade for plant to minimize heating and reduce water loss.
• In harmful levels of sunlight, specialised leaves, opaque or partly buried, admit light through a translucent leaf window for photosynthesis at inner leaf surfaces (e.g. Fenestraria).
• Succulent leaves store water and organic acids for use in CAM photosynthesis.
• Aromatic oils, poisons or pheromones produced by leaf borne glands deter herbivores (e.g. eucalypts).
• Inclusions of crystalline minerals deter herbivores (e.g. silica phytoliths in grasses, raphides in Araceae).
• Petals attract pollinators.
• Spines protect the plants (e.g. cacti).
• Special leaves on carnivorous plants are adapted to trapping food, mainly invertebrate prey, though some species trap small vertebrates as well (see carnivorous plants).
• Bulbs store food and water (e.g. onions).
• Tendrils allow the plant to climb (e.g. peas).
• Bracts and pseudanthia (false flowers) replace normal flower structures when the true flowers are greatly reduced (e.g. Spurges).
• Spathe.

Seasonal leaf loss

Leaves shifting color in autumn/fall

A girl playing with leaves

Leaves in temperate, boreal, and seasonally dry zones may be seasonally deciduous (falling off or dying for the inclement season). This mechanism to shed leaves is called abscission. When the leaf is shed, it leaves a leaf scar on the twig. In cold autumns, they sometimes change color, and turn yellow, bright-orange, or red, as various accessory pigments (carotenoids and xanthophylls) are revealed when the tree responds to cold and reduced sunlight by curtailing chlorophyll production. Red anthocyanin pigments are now thought to be produced in the leaf as it dies, possibly to mask the yellow hue left when the chlorophyll is lost—yellow leaves appear to attract herbivores such as aphids. Optical masking of chlorophyll by anthocyanins reduces risk of photo-oxidative damage to leaf cells as they senesce, which otherwise may lower the efficiency of nutrient retrieval from senescing autumn leaves.

Interactions with other organisms

Some insects, like Kallima inachus, mimic leaves

Leaf damaged by insects with chewing mouthparts, probably weevils or katydids

Although not as nutritious as other organs such as fruit, leaves provide a food source for many organisms. The leaf is a vital source of energy production for the plant, and plants have evolved protection against animals that consume leaves, such as tannins, chemicals which hinder the digestion of proteins and have an unpleasant taste. Animals that are specialized to eat leaves are known as folivores.

Some species have cryptic adaptations by which they use leaves in avoiding predators. For example, the caterpillars of some leaf-roller moths will create a small home in the leaf by folding it over themselves. Some sawflies similarly roll the leaves of their food plants into tubes. Females of the Attelabidae, so-called leaf-rolling weevils, lay their eggs into leaves that they then roll up as means of protection. Other herbivores and their predators mimic the appearance of the leaf. Reptiles such as some chameleons, and insects such as some katydids, also mimic the oscillating movements of leaves in the wind, moving from side to side or back and forth while evading a possible threat.

See also

• Glossary of plant morphology:Leaves
• Cladode - a flattened photosynthetic stem, if very leaf-like then it is called a phylloclade
• Cladophyll – a stem-like leaf part (synonym: phyllode)
• Crown (botany)
• Evolution of leaves
• Leaf Area Index
• Leaf protein concentrate
• Leaf sensor – a device that measures the moisture level in plant leaves
• Leaf shape
• Vernation – sprouting of leaves, also the arrangement of leaves in the bud

References

Bibliography

• "Leaves". , in Massey & Murphy (1996)
• Massey, Jimmy R.; Murphy, James C. (1996). "Vascular plant systematics". NC Botnet. University of North Carolina at Chapel Hill. Retrieved 19 January 2016. 
• Ghillean Tolmie Prance (1985). Leaves: The formation, characteristics and uses of hundred of leaves in all parts of the world. Thames and Hudson: (London) ISBN 0-500-54104-3. 256 pp. with 324 photographic plates in black and white, and colour by Kjell B Sandved
• Esau, Katherine (2006) [1953]. Evert, Ray F, ed. Esau's Plant Anatomy: Meristems, Cells, and Tissues of the Plant Body: Their Structure, Function, and Development (3rd. ed.). New York: John Wiley & Sons Inc. ISBN 9780470047378. 
• Rudall, Paula J. (2007). Anatomy of flowering plants: an introduction to structure and development (3rd ed.). Cambridge: Cambridge University Press. ISBN 9780521692458. 
• Geneve, Robert. "Leaf" (PDF). PLS 220: Intoduction to plant identification. University of Kentucky: Department of Horticulture. 
• Simpson, Michael G. (2011). Plant Systematics. Academic Press. ISBN 0-08-051404-9. 
• Cutter, E.G. (1969). Plant Anatomy, experiment and interpretation, Part 2 Organs. London: Edward Arnold. p. 117. ISBN 0713123028. 

External links

•  Ernest Ingersoll (1920). "Leaves". Encyclopedia Americana. 
• Science aid: Leaf Leaf structure and transpiration resource for teens.
• Cleared Leaves DB An open database for cleared leaves with full annotation.

English Journal

• [Predictive factors of esophagojejunal fistula after total gastrectomy in gastric cancer patients].

• Ben Maamer A, Zaafouri H, Noomene R, Haoues N, Bouhafa A, Oueslati A, Cherif A.
• La Tunisie médicale.Tunis Med.2013 Apr;91(4):263-8.
• BACKGROUND: The main complication observed after total gastrectomy is the oesophagojejunal anastomosic fistla. Its incidence varies between 7.4% and 11.5%. The mortality after anastomic leafage is high at around 20%, representing 30% and 54% of global mortality after total gastrectomy.AIM: This stud
• PMID 23673706

• [Determination of trace chromium and nickel in human hair using FAAS with flow injection extraction system].

• Chen S1, Wu R, Lin S.
• Guang pu xue yu guang pu fen xi = Guang pu.Guang Pu Xue Yu Guang Pu Fen Xi.1999 Feb;19(1):78-80.
• Trace amount of chromium and nickel was determined using a flow injection on-line extraction FAAS system. The measurement sensitivity for Cr and Ni increased by a factor of 20.1 and 14.3 respectively. For the national standand human hair sample and peach leafage sample, the measurement results are s
• PMID 15818924

• Effect of Leaf Position and Age on the Essential Oil Quantity and Quality in Lemongrass (Cymbopogon flexuosus)1.

• Singh N1, Luthra R, Sangwan RS.
• Planta medica.Planta Med.1989 Jun;55(3):254-6.
• The amount and composition of the essential oil of CYMBOPOGON FLEXUOSUS (lemongrass) leaves at different positions in the tiller and at different developmental stages were investigated. The results showed that only young leaves are biogenetically active, and that the leafage and leaf position are im
• PMID 17262411

Japanese Journal

• 北海道の秋まきコムギにおける分げつ性に関する研究:－第1報 分げつ追跡手法の検討と分げつ出現時期が穂形成・収量に及ぼす影響－

• 荒木 英晴
• 日本作物学会紀事 84(1), 34-40, 2015
• 秋まきコムギの分げつ性は，暖地ではいくつかの知見が報告されているが，北海道のような長期積雪地帯では調査事例は知られていない．これは，積雪期間が4～5ヶ月と長い北海道では労力的に分げつ追跡が困難であることや，簡易で有効な追跡手法が検討されていないためである．そこで本研究は，北海道の秋まきコムギ品種きたほなみを用い，簡易的な分げつ追跡手法を検討した．更に，この分げつ追跡手法を用いて，分げつ出現時期が穂 …
• NAID 130004829743

• イオン交換と膜透過現象

• 井川 学
• 日本イオン交換学会誌 19(2), 70-80, 2008
• 膜分離は省エネルギー, 省スペースで環境負荷の小さな技術であり, 現在, 電気透析や逆浸透法として広く使われている。膜分離法が生体膜のように, 高い選択透過性や能動輸送が可能になるなら, さらに広く使われるであろう。イオン交換は膜透過において最も基本的な分離支配要因の一つであるが, この論文では膜化学におけるイオン交換に関連する我々の研究を概説する。<BR>ある溶質と特異的に反応するイ …
• NAID 130004061619

• 全林野労働組合編 『樹海からの告発《林野黒書》』を読んで, 社会新報出版, B六版, 二二七頁, 定価四八〇円

• 吉沢 四郎
• 林業經濟 24(1), 41-45, 1971-01-20
• NAID 110009876980

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