65-591: Tannen [REDACTED] Origin Language(s) German Meaning fir Region of origin Germany Other names Variant form(s) Tanne , Tannenbaum , Jedlík , Jedlička , Jedliček Related place names Jedlicze [1] Tannen is surname of: Biff Tannen , a character in the Back to
130-408: 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
195-515: 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
260-463: A plant matures; as a case in point 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 atmospheric carbon dioxide. In most plants, leaves also are
325-419: A regular organization at the cellular scale. Specialized cells that differ markedly from surrounding cells, and which often synthesize specialized products such as crystals, are termed idioblasts . 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
390-475: A scaffolding matrix imparting mechanical rigidity to leaves. 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) which have diverse structures and functions. The major tissue systems present are These three tissue systems typically form
455-541: 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 heavily morphologically from
520-402: A single (sometimes more) primary vein in the centre 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
585-578: 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
650-533: A single point. In evolutionary terms, early emerging taxa tend to have dichotomous branching with reticulate systems emerging later. Veins appeared in the Permian period (299–252 mya), prior to the appearance of angiosperms in the Triassic (252–201 mya), during which vein hierarchy appeared enabling higher function, larger leaf size and adaption to a wider variety of climatic conditions. Although it
715-622: A small genus confined to eastern Asia. The genus name is derived from the Latin "to rise" in reference to the height of its species. The common English name originates with the Old Norse fyri or the Old Danish fyr . They are large trees, reaching heights of 10–80 metres (33–262 feet) tall with trunk diameters of 0.5–4 m (1 ft 8 in – 13 ft 1 in) when mature. Firs can be distinguished from other members of
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#1732794624928780-409: 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". Veins (sometimes referred to as nerves) constitute one of the most visible features of leaves. The veins in a leaf represent
845-405: 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
910-483: 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
975-1776: A very attractive combination valued in ornamental trees. The oldest pollen assignable to the genus dates to the Late Cretaceous in Siberia, with records of leaves and reproductive organs across the Northern Hemisphere from the Eocene onwards. A. bracteata (Don) Poit. A. mariesii Masters A. amabilis (Douglas ex Loudon) Forbes A. procera Rehder A. magnifica Murray A. concolor (Gordon) Lindley ex Hildebr. A. jaliscana (Martínez) Mantilla, Shalisko & Vázquez A. guatemalensis Rehder A. hickelii Flous & Gaussen A. flinckii Rushforth A. vejarii Martínez A. durangensis Martínez A. religiosa (Kunth) von Schlechtendal & von Chamisso A. hidalgensis Debreczy, Rácz & Guízar A. grandis (Douglas ex Don) Lindley A. lowiana (Gordon) Murray A. alba Miller A. pinsapo Boiss. A. cephalonica Loudon A. nebrodensis (Lojac.) Mattei A. nordmanniana (Steven) Spach A. numidica de Lannoy ex Carrière A. ×borisii-regis Mattf. A. cilicica (Antoine & Kotschy) Carrière A. lasiocarpa (Hooker) Nuttall A. ernestii Rehder A. balsamea (von Linné) Miller A. firma Siebold & Zuccarini A. sibirica Ledeb. A. fanjingshanensis Huang, Tu & Fang A. ziyuanensis Fu & Mo Leaves A leaf ( pl. : leaves )
1040-440: Is A. alba , and an example species with matt waxy leaves is A. concolor . The tips of leaves are usually more or less notched (as in A. firma ), but sometimes rounded or dull (as in A. concolor , A. magnifica ) or sharp and prickly (as in A. bracteata , A. cephalonica , A. holophylla ). The leaves of young plants are usually sharper. The leaves are arranged spirally on
1105-402: Is a principal appendage of the stem of a vascular plant , usually borne laterally above ground and specialized for photosynthesis . Leaves are collectively called foliage , as in "autumn foliage", while the leaves, stem, flower, and fruit collectively form the shoot system. In most leaves, the primary photosynthetic tissue is the palisade mesophyll and is located on the upper side of
1170-460: Is called a stipe in ferns . The lamina is the expanded, flat component of the leaf which contains the chloroplasts . The sheath is a structure, typically at the base that fully or partially clasps the stem above the node, where the leaf is attached. Leaf sheathes typically occur in Poaceae (grasses) and Apiaceae (umbellifers). Between the sheath and the lamina, there may be a pseudopetiole ,
1235-419: Is different from Wikidata All set index articles Fir See text Firs are evergreen coniferous trees belonging to the genus Abies ( Latin: [ˈabieːs] ) in the family Pinaceae . There are approximately 48–65 extant species, found on mountains throughout much of North and Central America , Eurasia, and North Africa . The genus is most closely related to Keteleeria ,
1300-406: 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
1365-425: The bract scales of the cones are long and exserted, or short and hidden inside the cone. Firs can be distinguished from other members of the pine family by the unique attachment of their needle-like leaves to the twig by a base that resembles a small suction cup . The leaves are significantly flattened, sometimes even looking like they are pressed, as in A. sibirica . The leaves have two whitish lines on
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#17327946249281430-494: 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 frigid or cold temperate regions typically shed their leaves in autumn, whereas in areas with
1495-424: The gymnosperms and angiosperms . Euphylls are also referred to as macrophylls or megaphylls (large leaves). A structurally complete leaf of an angiosperm consists of a petiole (leaf stalk), 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 proximal stalk or petiole
1560-551: The phyllids of mosses and liverworts . 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 ,
1625-399: The plant 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 which supply as much of the leaf as possible, ensuring that cells carrying out photosynthesis are close to
1690-844: The Future trilogy Val Tannen (born 1953), Professor of Computer Science at the University of Pennsylvania Charles Tannen (1915–1980), American actor Deborah Tannen (born 1945), American academic and professor of linguistics Julius Tannen (1880–1965), comedian and father of Charles and William Tannen Karl Tannen [ de ] (1827–1904), German publisher and writer Steve Tannen (born 1968), American singer-songwriter Steven Olson Tannen (born 1948), American college and professional football player William Tannen See also [ edit ] Lake Tannen [REDACTED] Look up Tannen in Wiktionary,
1755-679: 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. and Bulbine mesembryanthemoides . Leaves also 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,
1820-583: 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
1885-458: 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
1950-406: 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
2015-485: 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 are flattened and have distinct upper ( adaxial ) and lower ( abaxial ) surfaces that differ in color, hairiness, the number of stomata (pores that intake and output gases), the amount and structure of epicuticular wax and other features. Leaves are mostly green in color due to
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2080-447: The bottom, each of which is formed by wax -covered stomatal bands. In most species, the upper surface of the leaves is uniformly green and shiny, without stomata or with a few on the tip, visible as whitish spots. Other species have the upper surface of leaves dull, greyish green or bluish to silvery ( glaucous ), coated by wax with variable number of stomatal bands, and not always continuous. An example species with shiny green leaves
2145-606: 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
2210-558: 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 . Leaves which have a petiole (leaf stalk) are said to be petiolate . Sessile (epetiolate) leaves have no petiole and
2275-657: 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
2340-406: 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: Most divergence angles are related to the sequence of Fibonacci numbers F n . This sequence begins 1, 1, 2, 3, 5, 8, 13; each term is the sum of
2405-524: The free dictionary. [REDACTED] Surname list This page lists people with the surname Tannen . If an internal link intending to refer to a specific person led you to this page, you may wish to change that link by adding the person's given name (s) to the link. Retrieved from " https://en.wikipedia.org/w/index.php?title=Tannen&oldid=1092313212 " Categories : Surnames German-language surnames Hidden categories: Articles with short description Short description
2470-866: The ground, they are referred to as prostrate . 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. 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. Monocot leaves in temperate climates usually have narrow blades, and usually parallel venation converging at leaf tips or edges. Some also have pinnate venation. The arrangement of leaves on
2535-443: 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,
2600-523: 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
2665-551: The leaves of vascular plants . In most cases, they lack vascular tissue, are only 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
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2730-925: The majority, as broad-leaved or megaphyllous plants, which also include acrogymnosperms and ferns . In the lycopods , 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. 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. Some structures of non-vascular plants look and function much like leaves. Examples include
2795-404: The photosynthetic organelles , the chloroplasts , to light and to increase the absorption of carbon dioxide 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) openings called stomata which open or close to regulate
2860-403: The pine family by the way in which their needle-like leaves are attached singly to the branches with a base resembling a suction cup , and by their cones , which, like those of cedars , stand upright on the branches like candles and disintegrate at maturity. Identification of the different species is based on the size and arrangement of the leaves, the size and shape of the cones, and whether
2925-412: 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". External leaf characteristics, such as shape, margin, hairs, the petiole, and
2990-411: The presence of a compound called chlorophyll which is essential for photosynthesis as it absorbs light energy from the sun . A leaf with lighter-colored or white patches or edges is called a variegated leaf . Leaves can have many different shapes, sizes, textures and colors. The broad, flat leaves with complex venation of flowering plants are known as megaphylls and the species that bear them,
3055-434: 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 will usually continue to grow as long as they have
3120-410: The previous two. Rotation fractions are often quotients F n / F n + 2 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 φ = (1 + √5)/2 . When a circle is divided into two arcs whose lengths are in the ratio 1:φ , the angle formed by
3185-465: 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
3250-429: The primary veins run parallel and equidistant to each other for most of the length of the leaf and then converge or fuse (anastomose) towards the apex. Usually, many smaller minor veins interconnect these primary veins, but may terminate with very 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
3315-416: 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 very 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
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#17327946249283380-429: 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 . The internal organization of most kinds of leaves has evolved to maximize exposure of
3445-714: The rate exchange of carbon dioxide (CO 2 ), oxygen (O 2 ) 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. 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
3510-535: 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 . Where leaves are basal, and lie on
3575-470: The same species producing either green or purple cones: The cone scale bracts can be short and hidden in the mature cone, or long and exposed ('exserted'); this can vary even within a species, e.g. in Abies magnifica var. magnifica , the bracts are hidden, but in var. critchfieldii and var. shastensis , they are exserted. The bracts scales are often a different colour to the cone scales, which can make for
3640-446: 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
3705-455: The sequence 180°, 90°, 180°, 270°. 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,
3770-562: The shoots, but by being twisted at their base, the way they spread from the shoot is diverse; in some species comb-like ('pectinate'), with the leaves flat on either side of the shoot (e.g. A. alba , A. grandis ), in others, the leaves remain radial (e.g. A. pinsapo ) Foliage in the upper crown on cone-bearing branches is different, with the leaves shorter, curved, and sometimes sharp. Firs differ from other conifers in having erect, cylindrical cones 5–25 cm (2–10 in) long that disintegrate at maturity to release
3835-454: The smaller arc is the golden angle , which is 1/φ × 360° ≈ 137.5° . Because of this, many divergence angles are approximately 137.5° . 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
3900-421: The stem is known as phyllotaxis . A large variety of phyllotactic patterns occur in nature: 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
3965-547: 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
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#17327946249284030-511: 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
4095-632: The transportation system. Typically leaves are broad, flat and thin (dorsiventrally flattened), 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 . The flat, or laminar, shape also maximizes thermal contact with
4160-462: 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
4225-415: The winged seeds . In contrast to spruces , fir cones are erect; they do not hang, unless heavy enough to twist the branch with their weight. The mature cones are usually brown. When young in summer, they can be green: or reddish: or bloomed pale glaucous or pinkish: or purple to blue, sometimes very dark blue, almost black: Many species are polymorphic in cone colour, with different individuals of
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