Leaf

scan of a leaf Leaves are the most important organs of most vascular plants. Green plants are autotrophic, meaning that they do not obtain food from other living things but instead create their own food by photosynthesis. They capture the energy in sunlight and use it to make simple sugars, such as glucose and sucrose, from carbon dioxide () and water. The sugars are then stored as starch, further processed by chemical synthesis into more complex organic molecules such as proteins or cellulose, the basic structural material in plant cell walls, or metabolized by cellular respiration to provide chemical energy to run cellular processes. The leaves draw water from the ground in the transpiration stream through a vascular conducting system known as xylem and obtain carbon dioxide from the atmosphere by diffusion through openings called stomata in the outer covering layer of the leaf (epidermis), while leaves are orientated to maximize their exposure to sunlight. Once sugar has been synthesized, it needs to be transported to areas of active growth such as the shoots and roots. Vascular plants transport sucrose in a special tissue called the phloem. The phloem and xylem are parallel to each other, but the transport of materials is usually in opposite directions. Within the leaf these vascular systems branch (ramify) to form veins that supply as much of the leaf as possible, ensuring that cells carrying out photosynthesis are close to the transportation system. Typically leaves are broad, flat and thin (dorsiventrally flattened), thereby maximizing 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. The flat, or laminar, shape also maximizes thermal contact with the surrounding air, promoting cooling. Functionally, in addition to carrying out photosynthesis, the leaf is the principal site of transpiration, providing the energy required to draw the transpiration stream up from the roots, and guttation. Many conifers 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 favor 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. Leaves function to store chemical energy and water (especially in succulents) and may become specialized organs serving other functions, such as tendrils of peas and other legumes, the protective spines of cacti, and the insect traps in carnivorous plants such as Nepenthes and Sarracenia. Leaves are the fundamental structural units from which cones are constructed in gymnosperms (each cone scale is a modified megaphyll leaf known as a sporophyll) and from which flowers are constructed in flowering plants. that make them harder to degrade for microorganisms. The internal organization of most kinds of leaves has evolved to maximize exposure of the photosynthetic organelles (chloroplasts) to light and to increase the absorption of while at the same time controlling water loss. Their surfaces are waterproofed by the plant cuticle, and gas exchange between the mesophyll cells and the atmosphere is controlled by minute (length and width measured in tens of μm) stomata that open or close to regulate the rate exchange of , oxygen (O2), and water vapor 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. 3 - Spongy mesophyll 4 - Vein 5 - Xylem 6 - Phloem 7 - Collenchyma 8 - Chloroplasts 9 - Nucleus 10 - Vacuole 11 - Stomata 12 - Cuticle 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, available nutrients, and ecological competition from other plants. Considerable changes in leaf type occur within species, too, for example as a plant matures (Eucalyptus species commonly have isobilateral, pendent leaves when mature and dominating their neighbors; 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 . 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. 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 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 often 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 greatly morphologically from the leaves of vascular plants. In most cases, they lack vascular tissue, are a single cell thick and have no cuticle, stomata, or internal system of intercellular spaces. (The phyllids of the moss family Polytrichaceae are notable exceptions.) The phyllids of bryophytes are only present on the gametophytes, while in contrast the leaves of vascular plants are only present on the sporophytes. These can further develop into either vegetative or reproductive structures. Simple, vascularized leaves (microphylls), such as those of the early Devonian lycopsid Baragwanathia, first evolved as enations, extensions of the stem. 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 ==

'' (California redwood) '': Petiole, two stipules, rachis, five leaflets|alt=Leafstem of dog rose with petiole, stipules and leaflets '' leaves with translucent glands A structurally complete leaf of an angiosperm consists of a petiole (leaf stalk, called a stipe in ferns), a lamina (leaf blade), stipules (small structures located to either side of the base of the petiole) and a sheath. Not every species produces leaves with all of these structural components. The lamina is the expanded, flat component of the leaf that contains the chloroplasts. The sheath is a structure at the base that fully or partially wraps around the stem, above the node where the leaf is attached. Leaf sheathes typically occur in Poaceae (grasses), Apiaceae (umbellifers), and many palms. Between the sheath and the lamina, there may be a pseudopetiole, a petiole like structure. Pseudopetioles occur in some monocotyledons including bananas, palms and bamboos. Stipules may be conspicuous (e.g. beans and roses), soon falling or otherwise not obvious as in Moraceae or absent altogether as in the Magnoliaceae. A petiole may be absent (apetiolate), or the blade may not be laminar (flattened). 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". leaves External leaf characteristics, such as shape, margin, hairs, the petiole, and the presence of stipules and glands, are frequently important for identifying plants to family, genus or species levels, and botanists have developed a rich terminology for describing leaf characteristics. Leaves almost always 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 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 (Raphia regalis), which may be up to long and wide. The terminology associated with the description of leaf morphology is presented, in illustrated form, at Wikibooks. '' Where leaves are basal, and lie on the ground, they are referred to as prostrate. Basic leaf types Perennial plants whose leaves are shed annually are said to have deciduous leaves, while leaves that remain through winter are evergreens. Leaves attached to stems by stalks (known as petioles) are called petiolate, and if attached directly to the stem with no petiole they are called sessile. • Ferns have fronds. • Conifer leaves are typically needle- or awl-shaped or scale-like; they are usually evergreen but can sometimes be deciduous. Usually, they have a single vein. • The standard form of flowering plants (angiosperm) includes stipules, a petiole, and a lamina. • Lycophytes have microphylls. • Sheath leaves are the type found in most grasses and many other monocots. • Other specialized leaves include those of Nepenthes, a pitcher plant. Dicot leaves have blades with pinnate venation (where major veins diverge from one large mid-vein and have smaller connecting networks between them). Less commonly, dicot leaf blades may have palmate venation (several large veins diverging from petiole to leaf edges). Finally, some exhibit parallel venation. A large variety of phyllotactic patterns occur in nature: 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. '') are alternately arranged. ;Alternate: One leaf, branch, or flower part attaches at each point or node on the stem, and leaves alternate direction—to a greater or lesser degree—along the stem. ;Basal: Arising from the base of the plant. ;Cauline: Attached to the aerial stem. ;Opposite: Two leaves, branches, or flower parts attach at each point or node on the stem. Leaf attachments are paired at each node. ;Decussate: An opposite arrangement in which each successive pair is rotated 90° from the previous. ;Whorled, or verticillate: Three or more leaves, branches, or flower parts 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. In the simplest mathematical models of phyllotaxis, the apex of the stem is represented as a circle. Each new node is formed at the apex, and it is rotated by a constant angle from the previous node. This angle is called the divergence angle. The number of leaves that grow from a node depends on the plant species. When a single leaf grows from each node, and when the stem is held straight, the leaves form a helix. The divergence angle is often represented as a fraction of a full rotation around the stem. A rotation fraction of 1/2 (a divergence angle of 180°) produces an alternate arrangement, such as in Gasteria or the fan-aloe Kumara plicatilis. Rotation fractions of 1/3 (divergence angles of 120°) occur in beech and hazel. Oak and apricot rotate by 2/5, sunflowers, poplar, and pear by 3/8, and in willow and almond the fraction is 5/13. These arrangements are periodic. The denominator of the rotation fraction indicates the number of leaves in one period, while the numerator indicates the number of complete turns or gyres made in one period. For example: • 180° (or ): two leaves in one circle (alternate leaves) • 120° (or ): three leaves in one circle • 144° (or ): five leaves in two gyres • 135° (or ): eight leaves in three gyres. Most divergence angles are related to the sequence of Fibonacci numbers . This sequence begins 1, 1, 2, 3, 5, 8, 13; each term is the sum of the previous two. Rotation fractions are often quotients of a Fibonacci number by the number two terms later in the sequence. This is the case for the fractions 1/2, 1/3, 2/5, 3/8, and 5/13. The ratio between successive Fibonacci numbers tends to the golden ratio . When a circle is divided into two arcs whose lengths are in the ratio , the angle formed by the smaller arc is the golden angle, which is . Because of this, many divergence angles are approximately . In plants where a pair of opposite leaves grows from each node, the leaves form a double helix. If the nodes do not rotate (a rotation fraction of zero and a divergence angle of 0°), the two helices become a pair of parallel lines, creating a distichous arrangement as in maple or olive trees. More common in a decussate pattern, in which each node rotates by 1/4 (90°) as in the herb basil. The leaves of tricussate plants such as Nerium oleander form a triple helix. The leaves of some plants do not form helices. In some plants, the divergence angle changes as the plant grows. In orixate phyllotaxis, named after Orixa japonica, the divergence angle is not constant. Instead, it is periodic and follows the sequence 180°, 90°, 180°, 270°. Divisions of the blade 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 may be dissected to form 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. The leaflets may have petiolules and stipels, the equivalents of the petioles and stipules of leaves. 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: The leaflets all have a common point of attachment at the end of the petiole, radiating like fingers of a hand; for example, Cannabis (hemp) and Aesculus (buckeyes). ;Pinnately compound: Leaflets are arranged either side of the main axis, or rachis. ;Bipinnately compound: Leaves are twice divided: the leaflets (technically "subleaflets") are arranged along a secondary axis 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; for example, Albizia (silk tree). ;Trifoliate (or trifoliolate): A pinnate leaf with just three leaflets; for example, Trifolium (clover), Laburnum (laburnum), and some species of Toxicodendron (for instance, poison ivy). ;Pinnatifid: Pinnately dissected to the central vein, but with the leaflets not entirely separate; for example, Polypodium, some Sorbus (whitebeams). In pinnately veined leaves the central vein is known as the midrib. Characteristics of the petiole (Rheum rhabarbarum) are edible. Leaves that have a petiole (leaf stalk) 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 Eupatorium perfoliatum. 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: Veins leaf of a leaf skeleton Veins (sometimes referred to as nerves) constitute one of the most visible features of leaves. The veins in a leaf represent the vascular structure of the organ, extending into the leaf via the petiole and providing transportation of water and nutrients between leaf and stem, and play a crucial role in the maintenance of leaf water status and photosynthetic capacity. They also play a role in the mechanical support of the leaf. Within the lamina of the leaf, while some vascular plants possess only a single vein, in most this vasculature generally divides (ramifies) according to a variety of patterns (venation) and form cylindrical bundles, usually lying in the median plane of the mesophyll, between the two layers of epidermis. This pattern is often specific to taxa, and of which angiosperms possess two main types, parallel and reticulate (net like). In general, parallel venation is typical of monocots, while reticulate is more typical of eudicots and magnoliids ("dicots"), though there are many exceptions. The vein or veins entering the leaf from the petiole are called primary or first-order veins. The veins branching from these are secondary or second-order veins. These primary and secondary veins are considered major veins or lower order veins, though some authors include third order. Each subsequent branching is sequentially numbered, and these are the higher order veins, each branching being associated with a narrower vein diameter. In parallel veined leaves, the primary veins run parallel and equidistant to each other for most of the length of the leaf and then converge or fuse (anastomose) toward the apex. Usually, many smaller minor veins interconnect these primary veins but may terminate with fine vein endings in the mesophyll. Minor veins are more typical of angiosperms, which may have as many as four higher orders. In contrast, leaves with reticulate venation have a single (sometimes more) primary vein in the center of the leaf, referred to as the midrib or costa, which is continuous with the vasculature of the petiole. The secondary veins, also known as second order veins or lateral veins, branch off from the midrib and extend toward the leaf margins. These often terminate in a hydathode, a secretory organ, at the margin. In turn, smaller veins branch from the secondary veins, known as tertiary or third order (or higher order) veins, forming a dense reticulate pattern. The areas or islands of mesophyll lying between the higher order veins, are called areoles. Some of the smallest veins (veinlets) may have their endings in the areoles, a process known as areolation. These minor veins act as the sites of exchange between the mesophyll and the plant's vascular system. Thus, minor veins collect the products of photosynthesis (photosynthate) from the cells where it takes place, while major veins are responsible for its transport outside of the leaf. At the same time water is being transported in the opposite direction. The number of vein endings is variable, as is whether second order veins end at the margin, or link back to other veins. There are many elaborate variations on the patterns that the leaf veins form, and these have functional implications. Of these, angiosperms have the greatest diversity. Within these the major veins function as the support and distribution network for leaves and are correlated with leaf shape. For instance, the parallel venation found in most monocots correlates with their elongated leaf shape and wide leaf base, while reticulate venation is seen in simple entire leaves, while digitate leaves typically have venation in which three or more primary veins diverge radially from a single point. In evolutionary terms, early emerging taxa tend to have dichotomous branching with reticulate systems emerging later. Veins appeared in the Permian, prior to the appearance of angiosperms in the Triassic, during which vein hierarchy appeared enabling higher function, larger leaf size and adaption to a wider variety of climatic conditions. 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). In leaves with reticulate venation, veins form a scaffolding matrix imparting mechanical rigidity to leaves. 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, in contrast to; ;Heteroblasty: Characteristic in which a plant has marked changes in leaf size, shape, and growth habit between juvenile and adult stages. ==Anatomy==

Medium-scale features Leaves are normally extensively vascularized 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) having diverse structures and functions. Small-scale features The major tissue systems present are • The epidermis, which covers the upper and lower surfaces • The mesophyll tissue, which consists of photosynthetic cells rich in chloroplasts. (also called chlorenchyma) • The arrangement of veins (the vascular tissue) These three tissue systems typically form a regular organization at the cellular scale. Specialized cells that differ markedly from surrounding cells, and that often synthesize specialized products such as crystals, are termed idioblasts. Major leaf tissues File:Bifacial leaf cross section.jpg|Cross-section of a leaf File:Leaf epidermis 2.jpg|Epidermal cells File:Leaf spongy mesophyll.jpg|Spongy mesophyll cells Epidermis 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 that 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 and secretion of metabolic compounds. 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. They 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 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. 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. 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. The pores or stomata of the epidermis open into substomatal chambers, which are connected to the intercellular air spaces between the spongy and palisade mesophyll cell, so that oxygen, carbon dioxide and water vapor can diffuse into and out of the leaf and access the mesophyll cells during respiration, photosynthesis and transpiration. Leaves are normally green, due to chlorophyll in chloroplasts in the mesophyll cells. Some plants have leaves of different colors due to the presence of accessory pigments such as carotenoids in their mesophyll cells. Vascular tissue 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 (glucose to sucrose) produced by photosynthesis in the leaf, out 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. Early in development they are dorsiventrally flattened with both dorsal and ventral surfaces. 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." Many dicotyledonous leaves show endogenously driven daily rhythmicity in growth. == Ecology ==

Biomechanics Plants respond and adapt to environmental factors, such as light and mechanical stress from wind. Leaves need to support their own mass and align themselves in such a way as to optimize their exposure to the sun, generally more or less horizontally. However, horizontal alignment maximizes exposure to bending forces and failure from stresses such as wind, snow, hail, falling debris, animals, and abrasion from surrounding foliage and plant structures. Overall leaves are relatively flimsy with regard to other plant structures such as stems, branches and roots. Both leaf blade and petiole structure influence the leaf's response to forces such as wind, allowing a degree of repositioning to minimize drag and damage, as opposed to resistance. Leaf movement like this may also increase turbulence of the air close to the surface of the leaf, which thins the boundary layer of air immediately adjacent to the surface, increasing the capacity for gas and heat exchange, as well as photosynthesis. Strong wind forces may result in diminished leaf number and surface area, which while reducing drag, involves a trade off of also reducing photosynthesis. Thus, leaf design may involve compromise between carbon gain, thermoregulation and water loss on the one hand, and the cost of sustaining both static and dynamic loads. In vascular plants, perpendicular forces are spread over a larger area and are relatively flexible in both bending and torsion, enabling elastic deforming without damage. Many leaves rely on hydrostatic support arranged around a skeleton of vascular tissue for their strength, which depends on maintaining leaf water status. Both the mechanics and architecture of the leaf reflect the need for transportation and support. Read and Stokes (2006) consider two basic models, the "hydrostatic" and "I-beam leaf" form (see Fig 1). Hydrostatic leaves such as in Prostanthera lasianthos are large and thin, and may involve the need for multiple leaves rather single large leaves because of the amount of veins needed to support the periphery of large leaves. But large leaf size favors efficiency in photosynthesis and water conservation, involving further trade offs. On the other hand, I-beam leaves such as Banksia marginata involve specialized structures to stiffen them. These I-beams are formed from bundle sheath extensions of sclerenchyma meeting stiffened sub-epidermal layers. This shifts the balance from reliance on hydrostatic pressure to structural support, an obvious advantage where water is relatively scarce. Long narrow leaves bend more easily than ovate leaf blades of the same area. Monocots typically have such linear leaves that maximize surface area while minimizing self-shading. In these a high proportion of longitudinal main veins provide additional support. Interactions with other organisms s, like Kallima inachus, mimic leaves. 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 that 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 create a small home in the leaf by folding it over themselves. Several other lepidopteran larvae modify leaves for shelter; perhaps the greatest variety of shelter types occurs among the skipper butterflies (Hesperiidae), which cut, fold, and bind leaves using silk. 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. Seasonal leaf loss 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. ==Evolutionary adaptation==

bracts are leaves that have evolved red pigmentation 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: • Waxy micro- and nanostructures on the surface reduce wetting by rain and adhesion of contamination (See Lotus effect). • Divided and compound leaves reduce wind resistance and promote cooling. • Hairs on the leaf surface trap humidity in dry climates and create a boundary layer reducing water loss. • Waxy plant cuticles reduce water loss. • Large surface area provides a large area for capture of sunlight. • In harmful levels of sunlight, specialized leaves, opaque or partly buried, admit light through a translucent leaf window for photosynthesis at inner leaf surfaces (e.g. Fenestraria). • Kranz leaf anatomy in plants that perform carbon fixation • 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 from herbivores (e.g. cacti). • Stinging hairs to protect against herbivory, e.g. in Urtica dioica and Dendrocnide moroides (Urticaceae). • Special leaves on carnivorous plants are adapted for 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, spathes in the Araceae and floral heads in the Asteraceae). ==Terminology==

Shape Edge (margin) The edge or margin is the outside perimeter of a leaf. The terms are interchangeable. Apex (tip) 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 toward 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 The leaf surface is also host to a large variety of microorganisms; in this context it is referred to as the phyllosphere. ;Lepidote: Covered with fine scurfy scales. Hairiness '') leaves are covered in dense, stellate trichomes. ) leaf '') leaves are sericeous. "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. ;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: Developing after the flowers ;Synanthous: Developing at the same time as the flowers Venation Classification A number of different classification systems of the patterns of leaf veins (venation or veination) have been described, ==See also==