Botany Terms Starting With C
Botany Glossary: C
C4 Photosynthesis
/ SEE-FOHR foh-toh-SIN-theh-sis / · C4 refers to the four-carbon compound first produced
C4 photosynthesis is a carbon-concentrating mechanism in which carbon dioxide is first fixed into four-carbon organic acids in mesophyll cells, then released at high concentration around Rubisco in bundle sheath cells, sharply reducing the oxygenase activity of Rubisco and the energy losses of photorespiration.
In standard C3 photosynthesis, the enzyme Rubisco fixes carbon dioxide directly but also reacts with oxygen, triggering photorespiration and wasting up to 30 percent of fixed carbon under hot, bright conditions. C4 plants such as maize (Zea mays), sugarcane (Saccharum officinarum), and sorghum (Sorghum bicolor) avoid this loss by using phosphoenolpyruvate carboxylase in mesophyll cells to capture carbon dioxide as oxaloacetate, a four-carbon acid, before shuttling it to bundle sheath cells. There, decarboxylation releases carbon dioxide at concentrations roughly 10 times higher than atmospheric levels, saturating Rubisco and nearly eliminating its oxygenase reaction.
This biochemical pump raises water-use efficiency as well, because stomata can remain more closed while still supplying adequate carbon dioxide for photosynthesis.
C4 photosynthesis evolved independently at least 60 to 70 separate times across flowering plant lineages, making it one of the most frequently repeated major metabolic innovations in plant evolution. Grasses alone account for more than 20 independent origins.
C4 photosynthesis is a more advanced or superior form of photosynthesis. C4 is an adaptation to specific environments, hot, bright, or arid habitats, and C3 photosynthesis remains more efficient than C4 in cool, shaded, or carbon-dioxide-enriched conditions.
In sorghum (Sorghum bicolor), C4 photosynthesis sustains net carbon assimilation rates above 40 micromoles of carbon dioxide per square meter per second under full sunlight. Maize grown at 35 degrees Celsius loses less than 5 percent of fixed carbon to photorespiration, compared with roughly 25 percent in a C3 crop such as wheat under the same conditions.
Calyculus
/ kal-IK-yoo-lus / · Latin calyculus (small calyx)
Calyculus is an accessory whorl of bract-like appendages positioned immediately below the true calyx in certain flowering plants, superficially resembling an outer set of sepals but arising from modified bracts rather than from sepal primordia.
The calyculus, also called an epicalyx, occurs in families including Rosaceae, Malvaceae, and Dipsacaceae, where it develops from stipular or bracteolar tissue distinct from the true sepals. Segment number varies by taxon: strawberry (Fragaria x ananassa) bears five calyculus lobes alternating with five true sepals, while some mallows carry six to many bractlets. Vascular traces supplying calyculus segments branch from the receptacle independently of those supplying the sepals, confirming the non-sepal identity of the structure.
In strawberry, the calyculus persists through fruit development and forms the leafy green crown visible on ripe fruit in markets.
In the genus Potentilla (cinquefoils), the calyculus segments are sometimes larger than the true sepals and can be mistaken for petals by casual observers. Botanists distinguish them by their position outside the sepal whorl and by their independent vascular supply traced back to the receptacle.
Explore Order Rosales →A calyculus is the same structure as the main calyx. The calyculus is a separate outer whorl arising from bracts, with its own vascular supply, and it alternates with rather than replaces the true sepals.
In common mallow (Malva sylvestris), a calyculus of three narrow bractlets sits just below the five true sepals. Those bractlets remain green and persist around the schizocarp fruit as it matures, and each measures roughly 3 to 5 millimeters in length.
Hibiscus & Mallow Flowers →Calyx
/ KAY-liks / · Greek kalyx (cup, husk)
Calyx is the collective term for all the sepals of a flower, forming the outermost whorl of floral organs and enclosing the petals, stamens, and carpels during bud development.
Sepals are typically green and photosynthetically active, protecting inner floral organs from desiccation, mechanical damage, and herbivores before the bud opens. In some species, sepals are petaloid and brightly pigmented to attract pollinators; in monkshood (Aconitum napellus), for example, the large blue-purple sepals are the primary visual signal to bumblebee visitors because the petals are reduced and hidden. After pollination, the calyx may be deciduous, as in poppies, or persistent, as in tomato (Solanum lycopersicum), where the five-lobed calyx remains attached at the base of the ripe fruit.
Sepal number, fusion, and persistence are taxonomically informative characters used in dichotomous keys and phylogenetic analyses.
In the genus Calyx-flowered bluebell, Clematis species bear no true petals at all; the showy white or purple structures that attract pollinators are petaloid sepals. Some Clematis vines produce up to eight of these colored sepals per flower, with each sepal reaching 3 to 5 centimeters in length.
The calyx is always shed as soon as a flower opens. In many species the calyx persists through fruit development; the papery calyx of tomatillo Physalis philadelphica even expands to enclose the entire mature fruit.
In a rosebud (Rosa species), five green sepals form a tight calyx that completely encloses the petals before the flower opens. Those sepals can reach 2 to 3 centimeters in length and bear glandular hairs that deter small insects from entering the bud before pollination.
Cambium
/ KAM-bee-um / · Medieval Latin cambium (exchange)
Cambium is a lateral meristem in vascular plants consisting of a cylinder of undifferentiated cells that divides to produce secondary xylem toward the inside and secondary phloem toward the outside, increasing stem and root diameter over time.
The vascular cambium contains two cell types: elongated fusiform initials that give rise to axial xylem and phloem elements, and shorter ray initials that produce radial rays for lateral transport. Divisions are strongly seasonal in temperate climates, generating earlywood with wide, thin-walled vessels in spring and latewood with narrow, thick-walled cells in late summer, a contrast that produces the annual rings used in dendrochronology. Bristlecone pines (Pinus longaeva) in the White Mountains of California have produced continuous cambial records spanning more than 5,000 years, making them the oldest known living trees with dateable ring sequences.
A second lateral meristem, the cork cambium or phellogen, arises outside the vascular cambium and generates the protective bark layers that replace the epidermis as stems thicken.
Andrew Ellicott Douglass, an astronomer at the University of Arizona, founded the field of dendrochronology in the early 1900s by recognizing that cambial ring widths in southwestern US conifers recorded past drought years. His ring chronologies from Douglas fir (Pseudotsuga menziesii) eventually extended the climate record back more than 2,000 years.
Cambium is wood. Cambium is a thin meristematic tissue that generates wood and bark; the wood itself is secondary xylem, a product of cambial activity rather than the cambium itself.
In coast redwood (Sequoia sempervirens), the vascular cambium adds roughly 2 to 3 centimeters of new wood radius per decade in vigorous trees. Cross-sections of old-growth redwood trunks reveal more than 2,000 annual rings, each pair of earlywood and latewood bands representing one full year of cambial activity.
Capitulum
/ kah-PIT-yoo-lum / · Latin capitulum, small head
Capitulum is a dense, head-like inflorescence in which numerous sessile florets are attached directly to a flattened or domed receptacle and are subtended by an involucre of bracts, giving the entire structure the appearance of a single flower.
Capitula are the defining inflorescence type of the family Asteraceae, the largest family of flowering plants with roughly 23,000 species. Two functional floret types typically occupy a single head: ray florets around the periphery bear a strap-shaped ligule that attracts pollinators, while disc florets in the center are tubular and bisexual, each producing a single achene fruit topped by a pappus of hairs or scales. In common sunflower (Helianthus annuus), a single capitulum can contain 1,000 to 2,000 individual florets, and the disc florets open in a centripetal spiral sequence over several days to maximize cross-pollination.
Not all capitula contain both floret types; dandelion (Taraxacum officinale) heads consist entirely of ray florets, while thistles bear only disc florets.
The spiral arrangement of disc florets in a sunflower capitulum follows a Fibonacci sequence, typically 34 clockwise spirals intersecting 55 counterclockwise spirals. This packing geometry, studied mathematically by Alan Turing in the 1950s, places the maximum number of florets in the minimum space.
A sunflower head is one huge flower. A sunflower head is a capitulum, a compact inflorescence of hundreds to thousands of individual florets, each capable of producing its own seed.
In common dandelion (Taraxacum officinale), the capitulum holds between 100 and 300 individual ray florets, all attached to a single receptacle about 1 to 2 centimeters wide. Each floret produces one achene tipped with a feathery pappus that can carry the seed more than 100 meters on a light breeze.
Carotenoid
/ kah-ROT-eh-noyd / · Latin carota, carrot; -oid, resembling
Carotenoid is a class of fat-soluble pigments, ranging in color from yellow to red, synthesized by plants, algae, and certain bacteria that absorb light in the blue and blue-green wavelengths to supplement chlorophyll and dissipate excess light energy as heat to protect photosynthetic membranes.
Carotenoids are 40-carbon isoprenoid molecules built from eight isoprene units and divided into two main groups: carotenes, which are pure hydrocarbons such as beta-carotene, and xanthophylls, which contain oxygen atoms and include lutein and zeaxanthin. Within the chloroplast, carotenoids bound to light-harvesting complexes transfer absorbed energy to chlorophyll a through resonance energy transfer, extending the usable spectrum of photosynthetically active radiation. Zeaxanthin, in particular, accumulates rapidly when light intensity exceeds the capacity of the Calvin cycle, quenching excited chlorophyll molecules and releasing excess energy as heat through a process called non-photochemical quenching.
Autumn leaf color in deciduous trees results partly from carotenoids that were present all summer but masked by chlorophyll; as chlorophyll degrades in October, yellow and orange carotenoids become visible in species such as ginkgo (Ginkgo biloba) and tulip poplar (Liriodendron tulipifera).
Flamingos (Phoenicopterus roseus) obtain their pink coloration entirely from dietary carotenoids, primarily canthaxanthin and astaxanthin, absorbed from the brine shrimp and algae they filter-feed. Captive flamingos fed a carotenoid-free diet gradually turn white within one to two years.
Carotenoids only color flowers and fruits orange or yellow. Carotenoids also protect photosynthetic membranes from light damage in green leaves, where they remain invisible throughout the growing season because chlorophyll masks their color.
In autumn, sugar maple (Acer saccharum) leaves display yellow and orange hues produced by carotenoids, primarily lutein and beta-carotene, that were present in the leaf all summer. Lutein typically accounts for roughly 40 to 50 percent of total carotenoid content in maple leaves, making it the dominant pigment revealed as chlorophyll breaks down.
Carpel
/ KAR-pel / · Greek karpos, fruit; -el, diminutive
Carpel is the basic female reproductive unit of a flowering plant, consisting of an ovary enclosing one or more ovules, a style through which the pollen tube grows, and a stigma that receives and germinates pollen grains.
Carpels are thought to have evolved from leaf-like organs that folded and fused along their margins to enclose ovules, a hypothesis supported by the leaf-like carpels of basal angiosperms such as Amborella trichopoda. One or more carpels form the pistil; when multiple carpels fuse into a single compound pistil, as in tomato (Solanum lycopersicum), the number of locules inside the ovary often reveals the original carpel count. Placentation patterns, the arrangement of ovules on the ovary wall, vary systematically among plant families and include axile, parietal, and free-central types that taxonomists use to distinguish genera and families.
After fertilization, the ovary wall differentiates into the pericarp, which may become fleshy as in a peach or dry and papery as in a poppy capsule, while the fertilized ovules develop into seeds.
Amborella trichopoda, a shrub native only to New Caledonia and considered the sister lineage to all other living angiosperms, bears carpels that are not fully sealed by fusion but instead close by secretion of a sticky exudate along the carpel margin. This condition, described by botanist Peter Endress in the 1990s, suggests that complete carpel closure evolved gradually rather than appearing fully formed in the earliest flowering plants.
Carpels and stamens are the same type of floral organ. Carpels are female organs that enclose ovules and produce fruits after fertilization, while stamens are male organs that produce pollen; the two are structurally and functionally distinct.
In a tulip (Tulipa gesneriana) flower, three fused carpels form a single compound ovary containing hundreds of ovules arranged in axile placentation. After pollination, that ovary develops into a three-chambered capsule roughly 3 to 5 centimeters long that splits open to release flat, papery seeds.
Cellulose
/ SEL-yoo-lohs / · Latin cellula, small room; -ose, carbohydrate suffix
Cellulose is a structural polysaccharide composed of long unbranched chains of glucose units linked by beta-1,4-glycosidic bonds, forming the primary load-bearing component of plant cell walls.
Cellulose chains hydrogen-bond laterally to form crystalline microfibrils roughly 3 to 5 nanometers in diameter, which are synthesized at the plasma membrane by rosette-shaped cellulose synthase complexes and deposited in successive layers with alternating orientations. This cross-laminate arrangement gives the cell wall tensile strength comparable to that of mild steel on a per-unit-mass basis; cotton fibers (Gossypium hirsutum), which are nearly pure cellulose, withstand tensile stresses of approximately 400 megapascals. Unlike starch, which uses alpha-1,4-glycosidic bonds and coils into a helical form that enzymes can readily digest, the beta-linkages of cellulose create a flat, ribbon-like chain that most animals cannot break down without microbial assistance.
Termites and ruminants digest cellulose only because symbiotic gut microorganisms secrete cellulase enzymes that cleave those beta bonds.
Wood pulp used to make paper is roughly 40 to 50 percent cellulose after lignin and hemicellulose are removed during processing. Each metric ton of standard printing paper requires approximately 2.5 metric tons of raw wood, reflecting how much non-cellulose material must be extracted to isolate the cellulose fibers.
Cell Wall Functions →Cellulose and starch are interchangeable plant carbohydrates. Cellulose uses beta-1,4-glycosidic bonds that form rigid, indigestible fibers for structural support, while starch uses alpha-1,4-bonds that coil into a form plants store as an energy reserve and most animals can digest directly.
Differences Between Plant and Animal Cells →In flax (Linum usitatissimum), stem fibers consist of bundles of cells with walls that are up to 80 percent cellulose by dry weight. Those fibers can reach 30 to 90 millimeters in length and have been woven into linen textiles for at least 30,000 years, as evidenced by dyed flax fibers recovered from Dzudzuana Cave in the Republic of Georgia.
Chlorophyll
/ KLOR-oh-fil / · Greek chloros, green; phyllon, leaf
Chlorophyll is a magnesium-containing porphyrin pigment found in the chloroplasts of plants and algae that absorbs red and blue light to drive the light-dependent reactions of photosynthesis.
Two principal forms operate in land plants: chlorophyll a, which absorbs light most strongly near 430 and 662 nanometers, and chlorophyll b, which absorbs near 453 and 642 nanometers and transfers captured energy to chlorophyll a. Both molecules consist of a porphyrin ring with a central magnesium ion that undergoes charge separation when struck by a photon, releasing high-energy electrons that enter the electron transport chain of the thylakoid membrane. Green wavelengths near 550 nanometers are reflected rather than absorbed, which is why chlorophyll-rich tissues appear green to human observers.
Chlorophyll degrades rapidly when magnesium is displaced by hydrogen under acidic conditions, a reaction that turns cooked green vegetables olive-brown and that proceeds noticeably within minutes at temperatures above 70 degrees Celsius.
Chlorophyll d, discovered in red algae in 1943 and later found to dominate in the cyanobacterium Acaryochloris marina, absorbs light at 710 nanometers, well into the far-red region of the spectrum. Acaryochloris thrives beneath colonies of sea squirts that filter out shorter wavelengths, leaving far-red light as the primary available energy source.
Chlorophyll absorbs green light most strongly. Chlorophyll absorbs red light most efficiently near 662 nanometers and blue light near 430 nanometers, reflecting green wavelengths, which is precisely why plants appear green.
In the floating fern Salvinia molesta, chlorophyll molecules are densely packed into chloroplasts within the upper leaf surface, which measures only about 1 to 2 centimeters across. Under full sunlight, those chloroplasts can absorb enough red and blue photons to fix carbon at rates exceeding 10 micromoles of carbon dioxide per square meter per second.
Colpi
/ KOL-py / · Latin colpus (fold, furrow) + plural -i
Colpi are elongated furrows on the surface of pollen grains that mark sites of germination and water exchange, and whose number, arrangement, and structure help botanists and paleobotanists identify plant taxa.
Colpi are characteristic furrows in the exine layer of pollen grains found primarily in eudicot species, distinguished from pores by having a length-to-width ratio greater than two to one. Pollen apertures are classified by number and arrangement as tricolpate, hexacolpate, or other configurations depending on the plant family. Colpi may be simple or compound, and their ultrastructure can be observed with electron microscopy to distinguish among related taxa.
Pollen morphology including colpi number and arrangement has been preserved in sediments for millions of years, allowing paleobotanists to reconstruct ancient plant communities and vegetation patterns.
Pollen grains bearing colpi are extraordinarily resistant to decay because their exine walls contain sporopollenin, one of the most chemically stable biological polymers known. Cores drilled from peat bogs in northern Europe have yielded identifiable colpate pollen grains more than 10,000 years old, giving researchers a detailed record of postglacial forest recovery.
Colpi are cracks caused by damaged pollen. They are genetically determined structures built into the pollen wall during development in the anther.
In European white oak (Quercus robur) pollen, three colpi are evenly spaced around the grain, a tricolpate arrangement typical of most eudicots. Each colpus spans roughly half the grain's polar length, and the pattern is consistent enough that oak pollen can be identified to genus from sediment cores taken hundreds of kilometers from the nearest living tree.
Colpus
/ KOL-pus / · Latin colpus (fold, groove)
Colpus is a single elongated aperture in the wall of a pollen grain, defined by a length-to-width ratio greater than two to one, through which the pollen tube emerges during germination.
A colpus is a single elongated aperture in the pollen grain wall that functions in water uptake and pollen tube emergence during germination. The colpus has a length greater than twice its width, distinguishing it from a porus, which is roughly isodiametric or nearly circular in shape. Its wall consists of an endoaperture and exoaperture separated by the sexine and nexine layers of the exine.
During pollen grain hydration, the colpus may widen slightly as water enters the pollen grain and osmotic pressure increases, reducing internal tension in the wall.
Ragweed (Ambrosia artemisiifolia), one of the most prolific allergenic plants in North America, produces tricolporate pollen grains in which each aperture combines a colpus with a central pore. A single ragweed plant can release more than one billion pollen grains in a single season, and the aperture structure of each grain is so consistent that allergists and palynologists use it as a diagnostic marker.
A colpus is a seed opening. A colpus is a precisely defined aperture in the outer wall of a pollen grain, not a structure found in seeds at all.
In common ragweed pollen, each of the three colpi is a narrow furrow running lengthwise along the grain's surface. During germination on a compatible stigma, the pollen tube typically emerges through one of these apertures within 30 minutes of hydration.
Companion Cell
/ kum-PAN-yun SEL / · Old French compaignon (one who shares bread)
Companion cell is a nucleate, metabolically active phloem cell that maintains the function of an adjacent enucleate sieve tube member and regulates the loading and unloading of sugars into the phloem transport stream.
Companion cells and their associated sieve tube members arise from an unequal division of a single phloem mother cell, so the two cell types share a common developmental origin and remain connected by numerous plasmodesmata. Because mature sieve tube members lose their nuclei and most organelles, companion cells supply the proteins, ATP, and regulatory molecules needed to keep the sieve tubes functional. In apoplastic loaders such as sugar beet (Beta vulgaris), specialized companion cells called transfer cells develop elaborate wall ingrowths that increase membrane surface area and accelerate sucrose uptake from the apoplast.
A single companion cell can support one or more sieve tube members, and the density of mitochondria in companion cell cytoplasm reflects the high energy demand of active phloem loading.
In some parasitic plants, such as dodder (Cuscuta species), haustorial connections penetrate host phloem and tap directly into the sieve tube network, bypassing the companion cell loading machinery entirely. This allows the parasite to divert photosynthate without triggering the host's normal phloem regulatory responses.
Companion cells carry sugar instead of sieve tubes. Companion cells support sieve tube members and regulate the loading or unloading of phloem sap, but the bulk flow of sugars moves through the sieve tubes themselves.
In sugar beet (Beta vulgaris) leaves, companion cells sit directly beside sieve tube members and contain dense cytoplasm packed with mitochondria. Transfer cell variants of companion cells in this species develop wall ingrowths that can increase the plasma membrane surface area by several fold, accelerating sucrose loading into the phloem.
Compound Leaf
/ KOM-pownd LEEF / · Latin componere, to put together; Old English leaf
Compound leaf is a leaf whose blade is divided entirely to the midrib or petiole into two or more discrete leaflets, all of which share a single axillary bud at the base of the common petiole.
In a compound leaf, each leaflet shares the same petiole and the same axillary bud at the point where the petiole meets the stem, which is the most reliable way to distinguish a true leaf from a leaflet during identification. Compound leaves come in different arrangements: pinnate leaves have leaflets arranged along the sides of a central rachis, as in black walnut (Juglans nigra), while palmate leaves have all leaflets radiating from a single point at the petiole tip, as in horse chestnut (Aesculus hippocastanum). Bipinnate leaves, seen in honey locust (Gleditsia triacanthos), carry leaflets on secondary rachises branching from the main rachis.
The compound form reduces wind resistance and may also help shed herbivorous insects more readily than a broad simple blade.
Sensitive plant (Mimosa pudica) has bipinnate compound leaves whose leaflets fold inward within seconds of being touched, a response driven by rapid turgor loss in specialized cells at the leaflet bases called pulvini. This movement is thought to startle or dislodge herbivorous insects before they can feed.
Each leaflet of a compound leaf is a separate leaf. Leaflets lack axillary buds at their bases; only the whole compound leaf has an axillary bud, located where the petiole joins the stem.
In black walnut (Juglans nigra), a single compound leaf carries 15 to 23 leaflets arranged along a central rachis that can reach 60 centimeters in length. A single axillary bud at the base of the entire petiole confirms that all those leaflets belong to one leaf.
Conifer
/ KON-ih-fer / · Latin conus, cone; ferre, to carry
Conifer is a woody gymnosperm that bears seeds on the exposed scales of cones rather than enclosed within a fruit, and whose leaves are typically needle-shaped or scale-like and persist through multiple growing seasons in most species.
Conifers are gymnosperms, meaning their seeds are not enclosed in an ovary and instead sit exposed on the scales of a woody cone. Male cones release large quantities of pollen, which wind carries to female cones where fertilization takes place. Seeds then develop over weeks or months before the cone opens and disperses them.
With roughly 630 living species, conifers dominate boreal forests across North America, Europe, and Asia, and include the tallest living tree, coast redwood (Sequoia sempervirens), which can exceed 115 meters in height.
The bristlecone pine (Pinus longaeva) of the White Mountains in California includes individual trees confirmed to be more than 5,000 years old, making them the oldest known non-clonal living organisms on Earth. Their extreme longevity is linked partly to the dense, resin-saturated wood that resists decay, insects, and fungal infection.
All conifers are evergreen. Several conifer genera, including larch Larix and dawn redwood Metasequoia, are deciduous and shed all their needles each autumn.
In coast redwood (Sequoia sempervirens), flat needle-like leaves persist for several years before being shed, and seeds develop on small woody cones roughly 2.5 centimeters long. Individual redwood trees can live more than 2,000 years, with trunk diameters exceeding 8 meters at the base.
Coriaceous
/ kor-ee-AY-shus / · Latin coriaceus (of leather)
Coriaceous describes a leaf or other plant part whose texture is thick, stiff, and leathery due to heavily reinforced cell walls and a dense internal structure.
Coriaceous leaves develop thick cell walls, multiple layers of palisade mesophyll, and reduced intercellular spaces that together create a leathery, tough texture resistant to tearing and water loss. This leaf structure commonly occurs in plants inhabiting Mediterranean climates, coastal dunes, tropical rainforest understory, and other environments with intense light, drought, salinity, or nutrient limitation. The waxy cuticle overlaying coriaceous leaves is often thicker than in soft-leaved species, providing additional protection against transpiration.
Holly (Ilex aquifolium), eucalyptus, and rhododendron all produce coriaceous leaves that can persist for multiple growing seasons, reducing the plant’s investment in annual leaf replacement.
Magnolia grandiflora, the southern magnolia native to the southeastern United States, produces coriaceous leaves up to 30 centimeters long that remain on the tree for two full years before dropping. The lower surface of each leaf is covered in dense rust-colored hairs that trap a humid boundary layer of air, further reducing water loss through the stomata.
Coriaceous leaves are diseased or desiccated. Leathery texture is a genetically programmed developmental trait in many healthy species adapted to challenging environments.
In coast live oak (Quercus agrifolia) of California's chaparral, leaves are coriaceous and persist year-round despite summer drought. Cuticle thickness in this species can reach 10 micrometers, roughly five times thicker than the cuticle of a typical mesophytic leaf, limiting water loss during the dry season.
Cork
/ KORK / · Latin cortex (bark, rind)
Cork is a protective tissue of dead, suberin-impregnated cells produced by the cork cambium on the outer surface of woody plant stems and roots, forming a waterproof and mechanically resistant barrier.
Cork tissue originates from the cork cambium, a secondary meristem that divides to produce layers of dead cells with suberin-impregnated walls arranged in radial files. Suberin is a waxy polymer that renders cork cells waterproof and resistant to gas diffusion, creating an effective barrier against pathogen invasion and water loss. Dead cells in mature cork contain air-filled lumens that provide insulation and buoyancy.
In commercial cork oak (Quercus suber), the bark can be harvested every 9 to 12 years without killing the tree, as the cork cambium continuously generates new protective layers beneath the harvested surface.
Portugal and Spain together supply more than 80 percent of the world's commercial cork, most of it harvested from cork oak (Quercus suber) trees that are not cut down but stripped of their outer bark by hand. A single cork oak can be harvested up to 15 times over its lifespan, which commonly exceeds 200 years.
Cork is made of living soft tissue. Mature cork cells are dead at functional maturity, and their walls are impregnated with suberin, making them waterproof and structurally rigid.
In cork oak (Quercus suber), the cork layer can reach 20 centimeters in thickness on older trunks, far thicker than the bark of most temperate trees. Each cork cell is dead at maturity, its lumen filled with air and its walls lined with suberin, which gives harvested cork its characteristic compressibility and near-impermeability to liquids.
Corm
/ KORM / · Greek kormos (trunk stripped of branches)
Corm is a short, solid, swollen underground stem that stores carbohydrates and other nutrients, enabling a plant to survive unfavorable seasons and regenerate shoots and roots when conditions improve.
A corm is a short, thick underground stem that stores carbohydrates, proteins, and minerals in its tissue, enclosed by a protective papery tunic derived from dried leaf bases. New shoots and roots emerge from buds located on the corm’s surface, supporting vegetative reproduction when growing conditions become favorable. Unlike a bulb, which consists mostly of fleshy leaf scales arranged in concentric layers around a compressed stem, a corm is solid stem tissue with scattered vascular bundles throughout.
Crocus, gladiolus, and taro (Colocasia esculenta) all rely on corms to survive seasonal drought or cold, drawing on stored reserves until photosynthesis can resume.
Taro (Colocasia esculenta) produces corms that can weigh more than 4 kilograms and have been cultivated as a staple food crop across Polynesia, Southeast Asia, and parts of Africa for at least 10,000 years. The corm is one of the oldest known cultivated plant organs, predating rice cultivation in several regions.
Corms and bulbs are the same structure. A corm is entirely solid stem tissue, while a bulb is composed mainly of fleshy leaf scales surrounding a small compressed stem.
In autumn crocus (Colchicum autumnale), a corm roughly 3 to 5 centimeters in diameter stores enough carbohydrate to push flowers above ground in autumn before any leaves appear. The following spring, new leaves photosynthesize and replenish the corm's reserves for the next dormant season.
Crocus →Corolla
/ koh-ROL-uh / · Latin corolla (small crown)
Corolla is the collective term for all the petals of a flower, forming the whorl that lies inside the calyx and outside the stamens, and whose color, shape, and scent attract pollinators to the reproductive organs.
The corolla is composed of petals that may be separate and distinct or completely or partially fused into tubes, funnels, or other shapes. Petal color, texture, ultraviolet markings, and volatilized scent compounds attract specific pollinators such as bees, butterflies, hummingbirds, or nocturnal insects. The corolla’s shape guides pollinators toward the flower’s reproductive organs and nectaries, increasing pollination efficiency.
Petals are typically sterile, modified leaves that lack the photosynthetic function of foliage leaves.
Bee orchid (Ophrys apifera) produces a corolla that mimics the shape, color, and texture of a female bee so precisely that male bees attempt to mate with the flower, transferring pollen in the process. This deceptive strategy requires no nectar reward, making it one of the most energy-efficient pollination systems known among flowering plants.
The corolla includes sepals. The corolla consists only of petals; sepals form the calyx, which is a separate and distinct whorl located outside the corolla.
In trumpet vine (Campsis radicans), five petals are fused into a tubular corolla roughly 7 centimeters long that fits the bill length of ruby-throated hummingbirds (Archilochus colubris), its primary pollinator. The orange-red color of the corolla is highly visible to hummingbirds but relatively inconspicuous to most insects, effectively filtering for the intended pollinator.
Japanese Morning Glory →Cotyledon
/ kot-ih-LEE-don / · Greek kotyledon (cup-shaped hollow)
Cotyledon is an embryonic leaf present in a seed that either stores nutrients for the germinating seedling or absorbs them from surrounding endosperm tissue, and whose number distinguishes the two major groups of flowering plants.
Monocotyledonous plants have a single cotyledon, which in grasses is highly modified into an absorptive scutellum that digests the starchy endosperm tissue. In dicotyledonous plants, two cotyledons store lipids, proteins, and carbohydrates that the embryo consumes during germination and early growth. The cotyledon’s vascular tissue connects to the embryonic root and shoot, delivering absorbed or stored nutrients to growing tissues.
As the seedling’s true leaves expand and begin photosynthesis, the cotyledons gradually shrivel and senesce.
Coconut palm (Cocos nucifera) has a single, highly modified cotyledon that absorbs liquid endosperm, the coconut water, and solid endosperm, the white flesh, from inside the massive seed. The cotyledon in this species can reach 30 centimeters in length and remains embedded within the seed coat throughout germination rather than emerging into the light.
Cotyledons are always the first green leaves that photosynthesize. In many species, such as peas and corn, the cotyledons remain below ground or inside the seed coat and never photosynthesize, functioning solely as nutrient storage or absorption organs.
In common bean (Phaseolus vulgaris), two thick cotyledons packed with starch and protein push above the soil surface during germination, a pattern called epigeal germination. Each cotyledon shrinks noticeably within 10 to 14 days as the seedling draws down its stored reserves and the first true leaves take over photosynthesis.
Cuticle
/ KYOO-tih-kul / · Latin cuticula (thin skin)
Cuticle cuticle is a thin, waxy layer covering the outside of leaves and young stems that reduces water loss and protects the plant from damage.
Plant epidermal cells secrete a hydrophobic layer composed of cutin, a polymer of fatty acids, along with embedded waxes that form a crystalline coating on the leaf surface. This multilayered barrier reduces transpirational water loss by up to 95 percent in some species, allowing plants to survive in arid and semi-arid environments. Gas exchange continues through stomata, which perforate the cuticle and allow CO2 uptake despite the waxy covering.
Cuticle thickness varies dramatically among species, ranging from less than 1 micrometer in shade-adapted plants to over 40 micrometers in desert species like creosote bush.
A plant cuticle is a waxy barrier made by epidermal cells. It helps land plants live in air without drying out rapidly.
The cuticle blocks all gas exchange. Gas exchange still occurs through stomata while the cuticle reduces water loss.
In cactus stems, a thick waxy cuticle helps slow water loss in dry air. The cuticle covers the outer epidermis and reduces evaporation.
Cactus Flowers →Cyme
/ SYM / · Scientific term used in plant morphology.
Cyme cyme is a flower cluster in which the main stem ends in a flower, so the central or upper flower usually opens first.
A cyme is a determinate inflorescence in which the main axis terminates in a single flower, after which growth continues from lateral branches below the terminal flower. This contrasts with a raceme, where the main axis continues growing indefinitely and producing flowers in acropetal sequence from base to apex. In a simple cyme, lateral branches may themselves terminate in flowers, repeating the pattern at progressively smaller scales.
The terminal flower of a cyme opens first because it develops first and is the most mature flower in the cluster, while flowers on lateral branches open sequentially afterward. Common botanical examples include helicoid cymes where branches coil to one side, and scorpioid cymes where branches alternate sides, both resulting from the indeterminate growth of lateral branches.
A cyme is determinate because the main axis ends in a flower. This makes its opening pattern different from a raceme.
A cyme opens from the bottom upward like many racemes. The central or terminal flower usually opens first.
In forget-me-not inflorescences, the terminal flower on the main axis opens first, followed by flowers on successive lateral branches in acropetal order. This determinate branching pattern where the main axis ends in a flower defines the cyme structure.
Cytokinin
/ sy-toh-KY-nin / · Greek kytos, cell; kinein, to move
Cytokinin is a plant hormone that tells cells to divide and grow, controls the development of buds and side shoots, and helps keep leaves green by slowing their breakdown.
Cytokinins are made mainly in the growing tips of roots and travel upward through the plant in water. They work closely with another hormone called auxin, together they determine whether a piece of plant tissue grows into a root or a shoot. When cytokinin levels are high relative to auxin, shoot buds are released and start growing.
Cytokinins were first studied through their ability to promote cell division. They also delay leaf aging in many plants.
Cytokinin only controls roots. It affects cell division, shoots, buds, and leaf aging.
In plant tissue culture, cytokinins can encourage shoot formation from groups of cells. They often act together with auxins to shape development.
