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Leaf

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This article is about the plant organ. See leaf (disambiguation) for other meanings.
The leaves of a Beech tree
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The leaves of a Beech tree

A leaf with laminar structure and pinnate venation
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A leaf with laminar structure and pinnate venation

In botany, a leaf is an above-ground plant organ specialized for photosynthesis. For this purpose, a leaf is typically flat (laminar) and thin, to expose the cells containing chloroplast (chlorenchyma tissue) to light over a broad area, and to allow light to penetrate fully into the tissues. Leaves are also the sites in most plants where respiration, transpiration, and guttation take place. Leaves can store food and water, and are modified in some plants for other purposes. The comparable structures of ferns are correctly referred to as fronds. Leaves are prominent in the human diet as leaf vegetables.

Leaf anatomy

A structurally complete leaf of an angiosperm consists of a petiole (leaf stem), a lamina (leaf blade), and stipules (small processes located to either side of the base of the petiole). The point at which the petiole attaches to the stem is called the leaf axil. Not every species produces leaves with all of these structural parts. In some 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 Leaf types, arrangements, and forms.

A leaf is considered to be a plant organ, typically consisting of the following tissues:

  1. An epidermis that covers the upper and lower surfaces
  2. An interior chlorenchyma called the mesophyll
  3. An arrangement of veins (the vascular tissue).

Epidermis

The epidermis is the outer multi-layered group of cells covering the leaf. It forms the boundary between the plant and the external world. The epidermis serves several functions: protection against water loss, 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 is usually transparent (epidermal cells lack chloroplasts) and coated on the outer side with a waxy cuticle that prevents water loss. The cuticle may be thinner on the lower epidermis than on the upper epidermis; and is thicker on leaves from dry climates as compared with those from wet climates.

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

The epidermis is covered with pores called stomata, part of a stoma complex consisting of a pore surrounded on each side by chloroplast-containing guard cells, and two to four subsidiary cells that lack chloroplasts. The stoma complex regulates the exchange of gases and water vapor between the outside air and the interior of the leaf. Typically, the stomata are more numerous over the abaxial (lower) epidermis than the (adaxial) upper epidermis.

Trichomes or hairs grow out from the epidermis in many species.

Mesophyll

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 (= 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: 

The pores or stomata of the epidermis open into substomatal chambers, connecting to air spaces between the spongy layer cells.

These two different layers of the mesophyll are absent in many aquatic and marsh plants. Even an epidermis and a mesophyll may be lacking. Instead for their gaseous exchanges they use a homogeneous aerenchyma (thin-walled cells separated by large gas-filled spaces). Their stomata are situated at the upper surface.

Leaves are normally green in color, which comes from chlorophyll found in plastids in the chlorenchyma cells. Plants that lack chlorophyll cannot photosynthesize.

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. After the leaf is shed, a leaf scar develops on the twig. In cold autumns they sometimes turn yellow, bright orange or red as various accessory pigments (carotenoids and anthocyanins) are revealed when the tree responds to cold and reduced sunlight by curtailing chlorophyll production.

Veins

The veins are the vascular tissue of the leaf and are located in the spongy layer of the mesophyll. They are typical examples of pattern formation through ramification.

The veins are made up of:

The xylem typically lies over the phloem. Both are embedded in a dense parenchyma tissue (= ground tissue), called pith, with usually some structural collenchyma tissue present.

Leaf morphology

Underside view of leaf
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Underside view of leaf

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 developing buds in the axils of these leaves.
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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 developing buds in the axils of these leaves.

Fallen autumn leaves
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Fallen autumn leaves

External leaf characteristics (such as shape, margin, hairs, etc.) are important for identifying plant species, and botanists have developed a rich terminology for describing leaf characteristics. These structures are a part of what makes leaves determinant, they grow and achieve a specific pattern and shape, then stop. Other plant parts like stems or roots are non-determinant, and will continue to grow as long as they have the resources to do so.

Leaves may be classified in many different ways, and the type is usually characteristic of a species, although some species produce more than one type of leaf. The terminology associated with describing leaf morphology is presented (with illustrations) at [Wikibooks].  

Basic leaf types

Arrangement on the stem

As a stem grows, leaves tend to appear arranged around the stem in a way that optimizes yield of light. In essence, leaves come off the stem in a spiral pattern, 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 a limit of 360° x 34/89 = 137.52 or 137° 30', an angle known mathematically as the 'golden angle'. In the series, the numerator gives the number of complete turns or gyres until the leaf arrives at the initial position. The denominator gives the number of leaves in the arrangement. This can be demonstrated by the following: The fact that an arrangement of anything in nature can be described by a mathematical formula is not in itself mysterious. Mathematics is the science of discovering numerical relationships and applying formulae to these relationships. The formulae themselves can provide clues to the underlying physiological processes that, in this case, determine where the next leaf bud will form in the elongating stem. However, we can more easily describe the arrangement of leaves using the following terms:
Leaves of the White Spruce (Picea glauca) are needle-shaped and the arrangement is spiral
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Leaves of the White Spruce (Picea glauca) are needle-shaped and the arrangement is spiral

Divisions of the lamina (blade)

Two basic forms of leaves can be described considering the way the blade is divided. A simple leaf has an undivided blade. However, the leaf shape may be one 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 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.
Characteristics of the petiole
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.

Characteristics of the stipule

Venation (arrangement of the veins)

Palmate-veined leaf
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Palmate-veined leaf

Vein skeleton of a Hydrangea leaf
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Vein skeleton of a Hydrangea leaf

There are two subtypes of venation, craspedodromus (the major veins stretch up to the margin of the leaf) and camptodromous (major veins come close to the margin, but bend before they get to it).


Leaf terminology

Chart illustrating leaf morphology terms
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Chart illustrating leaf morphology terms
Shape
See Leaf shape

Margins (edge)

The leaf margin is characteristic for a genus and aids in determining the species.

Tip of the leaf

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

Base of the leaf

Surface of the leaf

The surface of a leaf can be described by several botanical terms: The leaf surface is also host to a large variety of microorganisms; in this context it is referred to as the phyllosphere.

Hairiness ( Leaves can show several degrees of hairiness. The meaning of several of the following terms can overlap. See also : Trichome.
  • glabrous: no hairs of any kind present.
  • arachnoid, 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.
  • 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, lanose: with woolly hairs.
  • pilose: with soft, clearly separated hairs.
  • puberulent, puberulous: with fine, minute hairs.
  • pubescent: with soft, short and erect hairs.
  • scabrous, 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, 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.
  • villous: with long and soft hairs, usually curved.
  • woolly: with long, soft and tortuous or matted hairs.

Adaptations

The leaves of Poinsettia have evolved a red pigmentation in order to attract insects and birds to the central flowers, an adaptive function normally served by petals.
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The leaves of Poinsettia have evolved a red pigmentation in order to attract insects and birds to the central flowers, an adaptive function normally served by petals.

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

See also

External links

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