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"inflorescence" Definitions
  1. the mode of development and arrangement of flowers on an axis
  2. a floral axis with its appendages
  3. the budding and unfolding of blossoms : FLOWERING

1000 Sentences With "inflorescence"

How to use inflorescence in a sentence? Find typical usage patterns (collocations)/phrases/context for "inflorescence" and check conjugation/comparative form for "inflorescence". Mastering all the usages of "inflorescence" from sentence examples published by news publications.

Now her white inflorescence meristem is basically the Kardashian of the cultivar group.
They have estimated sales will amount to $3.17 to $4.7 per gram of inflorescence.
When young, this phallic inflorescence is one or two feet long, orange-brown, and points stiffly upward.
The plant is the world's largest unbranched inflorescence, or cluster of multiple flowers that looks like a single one.
Even compared to the average virtual pet raising game it's pretty simple, valuing its minimalistic look over an inflorescence of mechanics.
You might also like theJao Goe Oil, the Herbivore Jasmine Glowing Hydrating Oil, theKypris Body Elixir Inflorescence, and theBurt's Bees Body Oil.
The mix of high-quality oils in Kypris' Body Elixir is great, but inflorescence is what makes its high price tag worth it.
You might also like the Jao Goe Oil, the Herbivore Jasmine Glowing Hydrating Oil, the Kypris Body Elixir Inflorescence, and the Burt's Bees Body Oil.
Yet each flower head is actually composed of many tiny flowers displayed in a flat-topped umbel (an inflorescence in which each flower stalk emanates from a single point).
That inflorescence is a two-way street, and all of the food eaten on those plantations came to table through the labor of an extensive network of enslaved people.
The corpse flower hails from Sumatra and holds the record for largest unbranched inflorescence—basically that giant cluster of flowers arranged on the stem in the middle of the plant.
Instead of holding her tresses, as Botticelli's Venus does, Nguyen's figure grasps a thick purple stem (or, more accurately a "pseudostem"), which emerges from her vagina and is topped by a large purple inflorescence.
Most commonly it has radial inflorescence, but it also rarely has terminal inflorescence.
The pitchers themselves are unknown. Nepenthes mollis has a racemose inflorescence. The female inflorescence is unknown. The male inflorescence is densely covered with flowers and is described by Danser as "not robust" and "at last seemingly lateral".
The terminal inflorescence is three to thirty flowered. The branching of the inflorescence is mostly dichasial, with ascending pairs of flowering branches rising five nodes below. The entire inflorescence is corymbiform to cylindric, though in smaller plants the inflorescence is a simple, nearly naked cyme. The cymes are subtended by slender bracts measuring long.
The bases of the leaves are overlapping. The blades are flat with edges towards the stem. Their tips are often fine-pointed. ;Inflorescence Its inflorescence appears terminal, having the lowest bract of the inflorescence not appearing as a continuation of the stem.
An umbel is a type of indeterminate inflorescence. A compressed cyme, which is a determinate inflorescence, is called umbelliform if it resembles an umbel.
These are spherical, the male inflorescence a ball of stamens and the female inflorescence a ball of developing fruits growing beneath the male spheres.
The short leaves have ligules with jagged tips. The inflorescence is generally a dense, spikelike panicle of oval-shaped spikelets. The inflorescence is greenish white, darkening brownish as it matures.
The inflorescence is dense and narrow when new, spreading out and becoming diffuse, with some branches sticking straight out, with age. The base of the inflorescence is often sheathed within the top leaf, which spreads out beside it. The grass produces abundant seeds; an individual inflorescence is capable of bearing 10,000 seeds.
Pale yellow, slender, drooping; Inflorescence - racemes with few flowers.
The inflorescence is an open, spreading array of thin branches bearing small spikelets which have awns up to 3 centimeters long. Spikelets lower in the inflorescence stay within sheaths and do not bloom.
The inflorescence is a narrow or spreading series of spikelets.
The inflorescence is an umbel of white or cream flowers.
Both types of inflorescence are rough clusters of tiny flowers.
The inflorescence consists of solitary, binate, digitate, or panicled racemes.
The inflorescence is a densely packed, bullet shaped cluster of overlapping flowers, mainly hanging on long peduncles. Each inflorescence is generally 2 to 4 centimeters long. Each of the flowers has a dark-colored bract.
The inflorescence is a crowded, one-sided series of flattened spikelets.
The inflorescence is purple, and the flowers when open are pink.
The inflorescence of small flowers is a panicle with racemose terminations.
The shift from the vegetative to reproductive phase of a flower involves the development of an inflorescence meristem that generates floral meristems. Plant inflorescence architecture depends on which meristems becomes flowers and which become shoots. Consequently, genes that regulate floral meristem identity play major roles in determining inflorescence architecture because their expression domain will direct where the plant's flowers are formed. On a larger scale, inflorescence architecture affects the quality and quantity of offspring from selfing and outcrossing, as the architecture can influence pollination success.
A panicle may have determinate or indeterminate growth. This type of inflorescence is largely characteristic of grasses such as oat and crabgrass, as well as other plants such as pistachio and mamoncillo. Botanists use the term paniculate in two ways: "having a true panicle inflorescence" as well as "having an inflorescence with the form but not necessarily the structure of a panicle".
Orange or red staminodes (usually 2). The inflorescence stalk generally elongated and not branched. The fruits contain 3 to 5 seeds. The inflorescence stalk is triangular in cross-section and acutely angled; with three distinct longitudinal ridges.
The inflorescence is an open cluster of green spherical spikes each long.
The inflorescence of terminal racemes is long, with a deep pink corolla.
White, few, large, sepals fleshy and persistent; Inflorescence - small, racemes opposite leaves.
The inflorescence bears a single spikelet, or sometimes up to four spikelets.
The inflorescence has a single spike with white flowers and small fruits.
The spikelike inflorescence produces many pinkish flowers each about 3 millimeters wide.
The terminal and erect cymose inflorescence bears actinomorphic, hexamerous, dish-shaped flowers.
The plant blooms annually around the beginning of the rainy season. The flower bud emerges from the corm as a purple shoot, and later blooms as a purple inflorescence. The pistillate (female) and staminate (male) flowers are on the same plant and are crowded in cylindrical masses as an inflorescence. The top part is responsible for secreting mucus that gives off a putrid, pungent smell that is used to attract pollinating insects, the middle part of the inflorescence contains staminate, and the base of the inflorescence contains pistillate.
The flowering stem emerges from the ground to produce a bright red or pink inflorescence containing male and female flowers. The crowded flower heads are covered in scales. The inflorescence is up to 15 to 20 centimeters long.
Each inflorescence bears 5,000 to 10,000 flowers, so a large inflorescence may carry about 40,000 seeds, or one million seeds for the whole tree in a good flowering year—hundreds of millions for a healthy grove of trees.
The inflorescence is supported by a peduncle, the plant shaft that supports the inflorescence The peduncel can range in size from 27 to 37cm long (.9 to 1.2 feet) and 1.5 to 2cm (.6 to .78 inches) in diameter.
A. Inga umbellifera inflorescence B.-D. Inga semialata inflorescence, fruit, seed E. Inga cordistipula pollen F. Inga amazonica single flower G.-H. Inga barbata branch and single flower A list of selected species of the huge legume genus Inga.
The inflorescence is a spiraling spike of flowers. The stem in the inflorescence is covered in glandular hairs. Each flower has curving white, cream, or yellow-tinged petals nearly one centimeter in length. Blooming occurs in July and August.
The inflorescence consists of a 30 cm stem bearing scarlet, bell-shaped flowers.
The branches of the inflorescence produce many small clusters of tiny yellow flowers.
The inflorescence is up to in height, with yellow flowers during the summer.
They are sessile, very small, and yellow in color; Inflorescence - spikes; trees dioecious.
The inflorescence is generally a linear structure with parallel branches bearing small spikelets.
The inflorescence is an erect, dense umbel of many tiny bright yellow flowers.
The inflorescence is a dense, spreading array of purple-tinged yellowish flowers long.
The inflorescence is a rounded or oval cluster or series of clusters of spikelets. The fertile spikelet has an awn up to a centimeter long. The awns clumped closely together into a tuft gives the inflorescence its bristly, hairy appearance.
The structure of the male inflorescence has not been documented. An indumentum of red, brown or white hairs up to 1 mm long may be present on the laminar margins, pitchers (particularly lower ones), tendrils, and parts of the inflorescence.
Typically, the stigmas are no longer receptive when pollen is released which prevents self- fertilization. We also have Compound Spadix Inflorescence in which the axis is branched. Usually whole Inflorescence is covered by a stiff boat shaped path for example- Coconut.
Euphorbia cyathophora, known by various names including dwarf poinsettia, fire-on-the-mountain, and paintedleaf, is native to North and South America and naturalized elsewhere. They belong to the Cyathium type of inflorescence. Here, the inflorescence axis is convex in shape.
The inflorescence has leaf-like bracts subtending the individual flowers. The bracts gradually get smaller towards the tip of the inflorescence, are always longer than the flowers and the upper ones are often tinged purple. The inflorescence forms a pyramid-shaped terminal spike and is formed of axillary whorls. The calyx of each flower is five-lobed, the bluish-violet corolla has a long tube and is fused, with two lips.
Small herbaceous perennials. Leaves equitant (distichous and overlapping), isobifacial. Inflorescence a raceme. Calyculus present.
The inflorescence is made up of hairy green bracts and bright yellow pouched flowers.
As the fruit develops the peduncle of the inflorescence curls into a neat spiral.
Each inflorescence has fifty or more minute white flowers with yellowish-green, globose spurs.
The flower capitula have no ray florets, and appear on a terminal, branching inflorescence.
The calyces are large, turning dark purple, along with the stem of the inflorescence.
In some species of Artabotrys, indeed, fasciation and curvation of the inflorescence are common.
Inflorescence simple, laxly many-flowered, fertile part to 35 cm long, glandular puberulent, green.
Anthericum ramosum reaches on average a height of . The grass-like leaves are long and wide and are generally much shorter than the inflorescence. It has an erect, paniculate inflorescence. The flower spikes are branched (hence the Latin name ramosus), unlike Anthericum liliago.
Rachis, which is the main axis of the inflorescence, and peduncles are puberulent to somewhat tomentulose. Pedicel, a stem that attaches single flower the main stem of the inflorescence, is about 5–11 mm long and often glabrous. Close-up on flowers.
The inflorescence is a scorpioid cyme and it is subtended by a boat-like spathe.
The inflorescence is a loose cluster of purple-washed white flowers with yellow-spotted throats.
The inflorescence is periodically covered in brown bracts from which protrude tiny white spurred flowers.
The coiled inflorescence holds tubular yellow flowers up to long and wide at the face.
The inflorescence is an open, spreading array of hair-thin branches bearing millimeter-long spikelets.
The inflorescence is a cluster of brown spikelets each about 3 or 4 millimeters long.
Inflorescence elongate racemes 4–7 cm. Sepal tube is bell-shaped 1 cm in diameter.
The inflorescence resembles a candelabra, with bright yellow flowers in bloom between May and June.
The inflorescence holds a single white flower 2 to 5 centimeters wide when fully open.
The inflorescence is a tangled array of branches tipped with small reddish-brown spikelike flowers.
The inflorescence is a dense cluster of sepals and four white to pink round petals.
Image:Hohenbergia stellata.JPG Image:Hohenbergia stellata plant.JPG Image:Hohenbergia Stellata Inflorescence ksl.jpg Image:Hohenbergia stellata blooms from stem ksl.
The stigmas of the female flowers will be receptive on the first day of the bloom, when the pungent smell draws pollinating insects inside, and the inflorescence closes, trapping them for a night to allow the pollen deposited on the insect to be transferred to the stigmas. Later in the second day, the female flower is no longer receptive to pollens, the male flowers start to bloom, and the inflorescence opens again. This allows the pollen to be deposited on the emerging insects to pollinate other flowers, while preventing the pollen from the same inflorescence fertilising itself, preventing inbreeding. In 24–36 hours, after the first bloom of the inflorescence, the inflorescence's female flowers start developing into berries bright red fruiting bodies, and other parts of the inflorescence start wilting away.
Inflorescence-feeding insect herbivores shape inflorescences by reducing lifetime fitness (how much flowering occurs), seed production by the inflorescences, and plant density, among other traits. In the absence of this herbivory, inflorescences usually produce more flower heads and seeds. Temperature can also variably shape inflorescence development. High temperatures can impair the proper development of flower buds or delay bud development in certain species, while in others, an increase in temperature can hasten inflorescence development.
The inflorescence has a series of five to seven narrow, linear bracts, which are pale yellow stained with green spots. Farther up the inflorescence, there are long floral bracts that are longer than the ovary. The inflorescence is a simple raceme with about 20 to 25 flowers with green sepals and petals with purple veins. Oeceoclades longebracteata is a terrestrial species found growing on gritty sand in clear undergrowth in deciduous forests.
Many asteraceous plants have bracts at the base of each inflorescence. The term involucre is also used for a highly conspicuous bract or bract pair at the base of an inflorescence. In the family Betulaceae, notably in the genera Carpinus and Corylus, the involucre is a leafy structure that protects the developing nuts. Beggar-tick (Bidens comosa) has narrow involucral bracts surrounding each inflorescence, each of which also has a single bract below it.
The branched, monoecious inflorescence has a 12–30 cm long prophyll. The inflorescence develops within a woody, glabrous (hairless) spathe which eventually grows 70–105 cm in total length, and has a swollen portion at the end 61–81 cm long and 6–13 cm wide. This swollen portion is often coloured purplish and the whole spathe may sometimes be smooth or striate. The inflorescence has a 35–60 cm long peduncle.
Vegetatively, this species differs little from M. microstoma, but is distinguished from it by its bostrychoid inflorescence on a rachis which continues to grow and flower, whereas M. microstoma has a different inflorescence type and all the flowers on it open at the same time.
Dendrobium amboinense has pseudobulbs that reach about in height. They produce two or three leaves about long and about wide. The flowers, up to four per inflorescence, are produced on very short racemes. Both leafless and leaved pseudobulbs are capable of producing an inflorescence.
This information can be used to improve breeding programs for P. juncea. In addition, water stress also improves leaf and inflorescence tissue quality, while nitrogen rich fertilizer improves leaf, stem, and inflorescence tissue quality. Increased tissue quality is related to improvements in total yield.
The inflorescence consists of 16-36 sweetly scented white-cream or yellow showy flowers in axillary clusters. The inflorescence stalk is long with coarse longish hairs. The over-lapping bracts are long and inner bracts rust coloured. The pedicels are long and the pistil long.
The leaves are up to 30 centimeters long; the upper leaves longer than the lower. The leaves are green to gray- green. The inflorescence is a bunch of very hairy racemes each a few centimeters long. Parts of the inflorescence can be purplish in color.
Diagram of a panicle A panicle is a much-branched inflorescence. (softcover ). Some authors distinguish it from a compound spike inflorescence, by requiring that the flowers (and fruit) be pedicellate (having a single stem per flower). The branches of a panicle are often racemes.
Evolution of catkins: inflorescence morphology of selected Salicaceae in an evolutionary and developmental context. Frontiers in Plant Science. 2015; 6: 1030. Such a convergent evolution raises questions about what the ancestral inflorescence characters might be and how catkins did evolve in these two lineages.
The A. tessellata inflorescence bears flowers each with an orangish corolla and calyx with four lobes.
The inflorescence is a compound umbel with up to 50 rays bearing clusters of hairy flowers.
The inflorescence is a compound umbel of up to 50 rays bearing clusters of small flowers.
Myosotis scorpioides is also colloquially denominated scorpion grass because of the spiraling curvature of its inflorescence.
The female inflorescence has spongy bracteoles up to a centimeter long and inflated around the flowers.
The inflorescence is a narrow, dense cluster of appressed, upright branches bearing small, silky-haired spikelets.
At each node along the inflorescence is a cluster of tiny flowers, which are usually white.
The inflorescence is an array of thin branches bearing tiny spikelets each a few millimeters long.
The inflorescence of Pachypodium baronii is pedunculate, having a main axis to flower stalk. The inflorescence is congested, measures 16 cm (inch) by 40 (inch) in length by 40 cm (1.58-inch) to 4.5 cm (1.77-inch) to 12 cm (0.47-inch), and have 3 to 17 flowers. The inflorescence's peduncle, the stalk of an inflorescence or a stalk bearing a solitary flower in a one-flowered inflorescence, is pale green and terete, cylindrical but usually slightly tapering at both ends. It measures 7 mm (0.276-inch) to 20 mm (0.787-inch) in length by 4 mm (0.157-inch) to 6 mm (0.236-inch).
The inflorescence is of Pachypodium bicolor is pedunculate, having the stalk of an inflorescence. It is congested at by with 5 to 8 flowers. The peduncle, the stalk, is terete, cylindrical but usually slightly tapering at both ends, circular in cross-section, and smooth- surfaced. It measures .
Although this species is variable in appearance and easily hybridizes with other Castilleja species, it generally bears a brightly colored inflorescence of shaggy pink-purple or lavender flowers. The thin, erect bracts are usually tipped with the same color, giving the inflorescence the appearance of a paintbrush.
The flowers are a rich orange-red, 1.5 in long, growing in whorls of twelve on a 1 ft inflorescence. The calyx and the inflorescence stem are covered in dark purple hairs with glands, justifying its specific epithet "hirtella" (hairy), with the calyces remaining long after blooming.
It bears an erect inflorescence which curves as it becomes heavier in grain. Each inflorescence is divided into three or four nodes with three or four spikelets per node. Each spikelet is between one and two centimeters long, not counting a long awn about two centimeters long.
Sepals are ovate-lanceolate, up to 7 mm long, and 4 mm wide. Each male inflorescence bears approximately 100 flowers, whereas each female inflorescence bears around 60 flowers. Mature fruits are up to 2.5 cm long. The stem and leaves of N. jacquelineae are glabrous throughout.
There is often no stem, the erect or spreading leaves and inflorescence emerging from ground level. The thinly fleshy leaves may approach 20 centimeters long, their blades divided into leaflets made up of many small oval segments. The inflorescence bears an umbel of small yellowish flowers.
The stalk of each single flower is called a pedicel. A flower that is not part of an inflorescence is called a solitary flower and its stalk is also referred to as a peduncle. Any flower in an inflorescence may be referred to as a floret, especially when the individual flowers are particularly small and borne in a tight cluster, such as in a pseudanthium. The fruiting stage of an inflorescence is known as an infructescence.
The key diagnostic character of S. albovaginatus is its ivory-colored, membranaceous leaf sheaths. The inflorescence of S. albovaginatus is short and congested, appearing compressed between its lower primary inflorescence bracts. Another key morphological character of S. albovaginatus are its relatively long and numerous perianth bristles. Similar to S. albovaginatus, Schoenus aureus and Schoenus triticoides also have ivory-colored, membranaceous, loose leaf sheaths; however, the inflorescence shapes of the latter two species differ from that of S. albovaginatus.
Three years later Rodrigues synonymised the genus Syagrus with Cocos (it was resurrected in 1916 by Beccari). It is quite similar to Syagrus romanzoffiana, but differs by being smaller, with smaller leaves and inflorescence, but with much larger fruit and female flowers. Unlike the spiral placement of the racemes (branches) of the inflorescence in S. romanzoffiana, S. macrocarpa has its racemes unilaterally arranged. S. cocoides also is similar, but has smaller fruit and spirally placed racemes in the inflorescence.
The inflorescence is branched, and flowering time is in summer - from December to February in South Africa.
Inflorescences are racemes; despite producing about 200 flowers per inflorescence, each one produces only a few fruit.
The inflorescence is covered in glandular hairs. Each flower has small spoon-shaped petals and protruding stamens.
The inflorescence is a peduncle with 3-24 rays, each long, bearing miniascule 5-petaled yellow flowers.
Featherfoil lives in swamps, ditches, and shallow ponds, including beaver ponds, with relatively stable water levels. Inflorescence.
The inflorescence is a dense, coiled cyme of several flowers with soft-hairy sepals and white corollas.
The inflorescence is a thin cylindrical array of tiny spikelets, each up to 4 millimeters in length.
Flower stalks are tall. The male inflorescence is a panicle; the female inflorescence consists of short spikelets borne in burlike clusters, usually with two to four spikelets per bur. Buffalograss sends out numerous, branching stolons; occasionally, it also produces rhizomes. Roots are also numerous and thoroughly occupy the soil.
The inflorescence may contain many flower heads with white or blue-tinged ray florets that may dry pinkish. The California plant is not colonial and the caudex branches little or not at all. The inflorescence contains no more than 3 heads. The florets are white or pink-tinged.
It differs from R. donnell-smithii in its smaller stature, smaller fruit, and more compact inflorescence. The inflorescence is a panicle, but appears racemose because of the short lateral branches and pedicels.Alwyn H. Gentry. 1992. "Bignoniaceae: Part II (Tribe Tecomeae)". Flora Neotropica Monograph 25(part 2):1-373.
The pendant inflorescence consists of 7-14 white, pink to red flowers in a showy profusion in axillary clusters, or on old wood. Each inflorescence is held on stalk about long. The pedicel long, the perianth long, initially a cream-white and aging to pink. The pistil long.
It blooms in Summer and Spring, although it has also been seen blooming in the Winter and Autumn. The plant is monoecious, with both sexes in each flower. It has its flowers arranged in a flower head, a special type of inflorescence. Each branch bears only one inflorescence.
The inflorescence consists of 6-12 strongly scented white, pink or reddish brown clusters of flowers. Inflorescence are supported on a stem long covered in long soft hairs. The bracts surrounding the flowers are long. The pedicels are long with white hairs, occasionally with glands on the tips.
Amorphophallus titanum has the largest unbranched inflorescence, while the talipot palm (Corypha umbraculifera) forms the largest branched inflorescence, containing thousands of flowers; the talipot is monocarpic, meaning the individual plants die after flowering. The flower is sometimes called the "monster flower" for its parasitic tendencies and foul odor.
Kabuyea hostifolia has a corm that lacks a protective tunic. The leaves are all basal and usually number four, both the leaves and the inflorescence emerging from the same corm-scale, and being present simultaneously. The inflorescence is a raceme, each floret having white tepals and parts in sixes.
There is usually no stem but the inflorescence arises on a stemlike peduncle up to about 15 centimeters tall. The inflorescence is a compound umbel bearing many tiny white flowers with dark anthers. The fruit is an ovoid body a few millimeters long lined with prominent longitudinal ribs.
The pinnae in the middle of the leaf blade are long and in width. The inflorescence is branched to the 1st degree, has a peduncle long and wide, and has a prophyll long, wide, and covered in a brown tomentum. The young inflorescence develops in a glabrous, lightly striated, woody spathe which is in length and has an enlarged portion at the end which is long wide and ending in a short, sharply pointed tip. The axis (width?) of the inflorescence is long.
The inflorescence is a dense cluster of green or brown spikes packed tightly and indistinct from each other.
Grassbase - The World Online Grass Flora. The inflorescence is usually a cylindrical, spike-shaped panicle, rarely with branches.
Trees of Britain and Europe. Collins . Inflorescence Floral diagram of A. hippocastanum. The light green structure denotes nectary.
The inflorescence contains 2 to 5 flowers pressed between flattened green bracts.Didymochlamys. Selected Rubiaceae Tribes and Genera. Tropicos.
The inflorescence is a dense cluster of tiny white flowers with five-lobed white corollas with yellow appendages.
Pimelea congesta is a flowering plant in the Thymelaeaceae family. The specific epithet refers to the congested inflorescence.
The inflorescence produces hairless, tubular or funnel-shaped blue to purple flowers just over a centimeter in length.
The inflorescence is a cluster of rounded flowers with minute petals tucked inside a calyx of pointed sepals.
The Bottle palm also has a more complex inflorescence that branches in four orders, rather than H.vaughaniis three.
All flowers are monoecious and unisexual, producing a spike inflorescence. All inflorescences are subtended by shorter, proximal bracts.
Some species so closely resemble one another that scientific differentiation is by inflorescence detail; flower size, colour, etc.
The inflorescence is a dense panicle up to 10–15 cm with whitish flowers and red-tipped petals.
The inflorescence bears several small flowers with pale to bright yellow notched petals just a few millimeters long.
Female Enhalus acoroides bears only a single inflorescence, but the peduncle of a female flower is much longer.
The inflorescence is an open array of branches bearing spikelets densely coated in silky white or pink hairs.
The erect inflorescence is a spike of small flowers up to long which grows above the water's surface.
They are simple and are arranged alternately. The inflorescence are borne at the ends of branches. They are bright red in color and spring from the apex of the peduncles. Each infloresence has multiple peduncles, each with 3 to 6 flowers, for a total of 13 to 20 per inflorescence.
Atop the stem is a large, fleshy inflorescence with red-tinged green bracts that serve as leaves. Within the lobular inflorescence are one to five small flowers, each less than a centimeter long. The yellow-throated flower has yellow or white oval-shaped lobes with pointed tips. It is self-pollinating.
The pollinators always land at bottom of the inflorescence and visit the flowers ever higher up. Most bumblebees have a strong preference for counterclockwise arrangement, fewer for clockwise. It seems that autumn lady's tresses responds to this preference by offering different inflorescence types and thus increases the chances of fertilization.
In subsequent years it produces an upright flowering stem, unbranched until the base of the inflorescence. The stem is tough, grooved, green when young but turning reddish with age. Leaves growing on the stem are alternate, arching and decreasing in size higher up the stem. The inflorescence is a compound raceme.
The common example of this is most members of the very large composite (Asteraceae) group. A single daisy or sunflower, for example, is not a flower but a flower head—an inflorescence composed of numerous flowers (or florets). An inflorescence may include specialized stems and modified leaves known as bracts.
Lomatium torreyi is a perennial herb growing up to 30 centimeters tall from a long taproot. There is generally no stem, the leaves and inflorescence emerging at ground level. The leaf blades are divided and subdivided into a mass of threadlike segments. The inflorescence is an umbel of yellow flowers.
The lowest bract subtending the inflorescence is about the same length as the inflorescence. Carex rainbowii resembles the other species in Carex sect. Sylvaticae; compared to C. sylvatica, it has denser female spikes, and is distinguished by its hyaline female glumes and the fact that the uppermost spike is often androgynecandrous.
The inflorescence is a head of flowers up to 3 centimeters wide with white to purplish or bicolored corollas.
The inflorescence is a plumelike panicle up to 15 centimeters long containing many V-shaped spikelets with long awns.
The inflorescence is a spike studded with spikelets up to 3 centimeters long, each containing up to 12 flowers.
Inflorescence are showy of 15 to 20 on 32 inch long raceme.The Orchids of the Philippines J. Cootes 2001.
The inflorescence may approach in height. The small flowers each have six whitish tepals a few millimeters in length.
The inflorescence is a cluster of flowers with each minute white or yellow flower surrounded by spine-tipped bracts.
They grow long, plicate leaves. They produce an unbranched, erect, terminal inflorescence bearing usually white or yellow, nodding flowers.
The inflorescence has loosely clustered spikelets. The plant reproduces by seed and rhizome and it sometimes spreads via stolon.
Myosotis scorpioides is also known as scorpion grass due to the spiraling curve of its inflorescence on scorpiod cymes.
Its inflorescence is composed of two opposite triads, with the all the flowers being sessile. The leaves are flat.
Flowers - Inflorescence - male greenish, short racemose cymes; female more slender axillary or terminal cymes. Fruits - beaked, pear-shaped drupe.
Inflorescence is corymbose cymes. Corolla is white with purple color. Fruit is purplish black with four seeded smooth drupe.
They are clothed in the sheaths of the leaves. The inflorescence is cylindrical.Coelorachis cylindrica. USDA NRCS Plant Fact Sheet.
Its body lies on the ground and only a 10-20 cm long footstalk stands ending in an inflorescence.
Aiphanes species are pleonanthic—they flower repeatedly over the course of their lifespan—and monoecious, meaning that there are separate male and female flowers, but individuals plants bear both types of flowers. In Aiphanes, male and female flowers are borne together on the same inflorescence. Usually only a single inflorescence is borne at each node, although A. gelatinosa often bears then in groups of three at a single node. The inflorescence usually consists of a main axis consisting of a peduncle and a rachis.
The developing inflorescence is protected within a woody, hairless spathe which is lightly striated and 105–135 cm in total length, the swollen part of this spathe being 40–110 cm long and 7–14 cm wide. The branched inflorescence has a 40–75 cm long and 1.5-2.2 cm wide peduncle (stalk). The rachis of the inflorescence is 40–72 cm long and has 68-155 rachillae (branches) which are 16–72 cm long. The flowers are coloured yellow, yellow-purple, greenish-yellow or entirely purple.
Genes that shape inflorescence development have been studied at great length in Arabidopsis. LEAFY (LFY) is a gene that promotes floral meristem identity, regulating inflorescence development in Arabidopsis. Any alterations in timing of LFY expression can cause formation of different inflorescences in the plant. Genes similar in function to LFY include APETALA1 (AP1).
Leaves higher on the stem are much reduced. The upper part of the stem is a spikelike inflorescence of many delicate, translucent green flowers which are sometimes fragrant in the evenings. This rein orchid has narrower petals than those of other species, giving the inflorescence a lacy look, as the common names suggest.
The leaf margin is set with curved eyelashes. The conical to ovate inflorescence has a length of 10 to 25 centimeters and a diameter of 10 to 15 centimeters. The inflorescence stem is 5 to 20 inches long. The flowers sit on a 2 to 12 millimeters long, slightly fluffy flower stem.
Euphorbia nutans is an annual herb growing erect with pairs of oblong leaves along its stems. The leaf may be up to long, hairy or hairless, and finely toothed. The inflorescence may be solitary or borne in clusters. Each inflorescence is a cyathium, with flat white or red appendages surrounding the actual flowers.
The flowers are canary yellow, 2 cm wide, and have a lip lobed into three sections. Two of the outlying lobes are fimbriated. Usually 8-16 flowers are born on an inflorescence, with multiple racemes possible resulting in a flower count in the thousands. The flowers form two rows on the single inflorescence.
The leaf sheaths on the upper stem are swollen. The stalk of the inflorescence (peduncle) is 20-100 mm long and there are often several at a node. The axis of the inflorescence is 0.6-1.2 m by 0.1-0.3 m. The 10-30 stalks of individual flowers (pedicels) are 0.5 mm long.
The panicles inflorescence are two to three and a half meters high. The bright- yellow flowers are 45 to 50 mm long and appear on the upper half of the inflorescence in loose, variably arranged branches. The flower tube is 14 to 10 mm long. The blooming period is from June to July.
The shrub has a terminal inflorescence which is approximately 15–30 mm long. It is panicle-like and maintains a hemispheric shape. Holding the inflorescence and providing it support is a long stem, known as peduncle. It is typically 26–48 mm in length, usually with a few reduced leaves near the base.
The inflorescence is composed of a cluster of staminate flowers and a cluster of pistillate flowers separated by a node.
The tall (1m) erect inflorescence has up to 20 spreading branches, each with a cylindrical raceme of pink-red flowers.
Berteroa incana. Flora of North America. The leaves are hairy and grayish. The inflorescence is a dense raceme of flowers.
The plant is erect, often forming colonies. Flowers are small yellow heads held above the foliage on a branching inflorescence.
The flat leaf blades are up to 24 inches long. The ligule is pointed. The inflorescence is one-sided.Sorghastrum secundum.
The inflorescence arises on a peduncle up to half a meter tall and bears clusters of flowers with white petals.
Alangium circulare grows as a tree up to tall. The smooth bark is grey-brown. The inflorescence is greyish pubescent.
The inflorescence is a compound umbel of up to 60 long rays each bearing clusters of whitish or yellowish flowers.
The drooping inflorescence has narrow spikelets with awns up to 15 millimeters long which are often, but not always, crinkled.
The fruit is a slightly inflated hairy legume pod up to long which hangs in bunches from the dried inflorescence.
The inflorescence is a solitary tubular flower up to a centimeter long with a flat white or pale pink corolla.
The inflorescence bears pink to purple flowers which yield narrow siliques up to 4 centimeters long containing round, winged seeds.
Male flowers have free or connate (fused together) filaments. Fruits are capsules with one to three fruits occurring per inflorescence.
The spreading branches of the inflorescence hold oval-shaped to nearly round spikelets each with generally fewer than six florets.
The inflorescence is a wide cluster of flower heads, each enveloped in an involucre of rows of bright white phyllaries.
Chionanthus polycephalus is a tree in the family Oleaceae. The specific epithet polycephalus means "many-headed", referring to the inflorescence.
The inflorescence is a head of flowers lined with leaflike bracts. The lavender flowers are just under a centimeter long.
Additionally, the inflorescence produced has a smell of rotting meat.Bown, Demi (2000). Aroids: Plants of the Arum Family. Timber Press. .
The stems are often purplish toward the base. The inflorescence is white and hairy. The plant produces many seeds.Bothriochloa saccharoides.
The entire plant is hairless (glabrous). The flowers are unisexual, carried on the same inflorescence (i.e. the plant is monoecious).
Holochlamys closely resemble Spathiphyllum except that in Holochamys the spathe clasps the spadix. Also, the inflorescence rots quickly after flowering which doesn't occur in Spathiphyllum. The inflorescence emerges below the foliage and has a white spathe and spadix. The spadix tends to be about the same length as the spathe and produces a leathery fruit.
The species has male and female flowers on separate plants. The staminate inflorescence is a catkin up to long with fuzzy male flowers. The pistillate inflorescence is a spherical head up to about wide with greenish female flowers trailing long styles. The infructescence is a spherical cluster wide containing many red or orange fruits.
Claoxylon indicum is a pyramid-shaped shrub or small tree growing to 2–10 m in height. Its branches are grey and hairy, with large leaf scars. The leaves are oval and 80–300 mm long. The slender male inflorescence is 30–150 mm long, carrying many flowers; the female inflorescence 15–80 mm long.
Carex bigelowii produces 3-angled stems up to tall, growing in a tuft or singly. The leaves are stiff and dark green, and the leaves of previous seasons may remain on the plant. The inflorescence is accompanied by a short bract. The inflorescence has 1–3 black pistillate spikes under 1–2 staminate spikes.
The inflorescence in Xanthosoma is composed of a spadix with pistillate flowers at the base, a belt of sterile flowers offered as a reward for pollinators in the middle and staminate flowers on the upper part. Prior to opening, the inflorescence is enclosed within a leaf-like spathe. When the inflorescence is ready to open, the upper part of the spathe opens and exposes the staminate area of the spadix; the basal area of the spathe remains closed, forming a spacious chamber (i.e., the spathe tube) that encloses the pistillate and sterile flowers ().
The inflorescence of Vanda garayi, an epiphytic orchid, is a typical raceme A raceme ( or ) or racemoid is an unbranched, indeterminate type of inflorescence bearing pedicellate flowers (flowers having short floral stalks called pedicels) along its axis. In botany, an axis means a shoot, in this case one bearing the flowers. In indeterminate inflorescence-like racemes, the oldest flowers are borne towards the base and new flowers are produced as the shoot grows, with no predetermined growth limit. A plant that flowers on a showy raceme may have this reflected in its scientific name, e.g.
The entire leaf may be up to 3 m long. (The first two leaves on a seedling are simple, and are followed by several alternate compound leaves.) The upright female inflorescence is born terminally on the current year's growth, containing 40 to 50 blossoms. The male inflorescence is a catkin, up to 18 cm in length; it may grow alone from the current or previous year's growth, in a panicle of up to six paired catkins, or rarely at the base of an androgynous panicle, which ends in the female inflorescence.
The inflorescence is a spreading array of branches, the lower ones reflexed. The branches bear several rough-haired spikelets containing flowers.
The inflorescence is produced from the base of the pseudobulb, pendant, surrounded by 2 to 4 sheaths, 1 to 3-flowered.
The stem, lamina, and pitchers are glabrous. An inconspicuous indumentum of simple, rusty brown hairs (0.1 mm long) covers the inflorescence.
Flowers Inflorescence axillary solitary or racemes, 1–2 cm long; flowers sessile. Fruit& seed Drupe, cylindrical or ellipsoid, 1.1 cm long.
The inflorescence is a dense panicle usually no more than 1.5 centimeters long tucked into the sheaths of the uppermost leaves.
The lantern flower is closely related to the sympatric A. auritum; both have a paniculate inflorescence and fewer than 15 mericarps.
The inflorescence is a cluster of 6 to 9 tubular purple flowers, each with a face up to 1.5 centimeters wide.
The clublike inflorescence may exceed 4 centimeters in length and two in width. It is chunky and purple or purplish- green.
The top of the stem is occupied by the inflorescence, a cyme with several clusters of tiny white or pink flowers.
Terminal corymbs inflorescence. Pedicels are short, about 3–4 mm in length. Petals 5, white. Hypanthium with long furs, triangle shaped.
The inflorescence is coated in tentacle-like glands. Flowering occurs in spring and again in fall.Dalea tentaculoides. Center for Plant Conservation.
The inflorescence is slightly glandular, almost glabrous. The samarae are orbicular to obovate, with a few glandular hairs; the seed central.
The inflorescence is a wide array of nodding, flat spikelets, each on an individual stalk that may be curved or wavy.
The perianth of its flowers is noticeably constricted above its base, and it has an inflorescence of five or more branches.
Pachypodium inflorescence, or clusters of flowers, appear either at the end of the stem, growing directly off the stem, or attached to the stem by branchlets. The bracts, or leaves surrounding the inflorescence, resemble sepals. Flower stalks range in length from 0 to 56 mm. Pachypodium flowers always consist of five sepals, ranging in shape from ovate to oblong.
For example, Asclepias inflorescences have been shown to have an upper size limit, shaped by self- pollination levels due to crosses between inflorescences on the same plant or between flowers on the same inflorescence. In Aesculus sylvatica, it has been shown that the most common inflorescence sizes are correlated with the highest fruit production as well.
Aloe hereroensis, showing inflorescence with branched peduncle An inflorescence is a group or cluster of flowers arranged on a stem that is composed of a main branch or a complicated arrangement of branches.Guertin, P., Barnett, L., Denny, E.G., Schaffer, S.N. 2015. USA National Phenology Network Botany Primer. USA-NPN Education and Engagement Series 2015-001. www.usanpn.org.
It may be glandular and resinous and slightly woolly or hairless. Atop each of the many erect branches is an inflorescence of golden yellow flower heads. Each centimeter-wide head has up to 14 disc florets and sometimes up to 5 ray florets but sometimes none. The dense inflorescence has resin glands and some woolly fibers.
The inflorescence consists of 2-11 cream- white to golden yellow flowers in profusion, clustered along the branches. The inflorescence is on a simple stem densely covered with upright hairs, they may be white, brown or a combination of both. The pedicels are long with white, soft, silky hairs. The pistil long, the perianth is smooth and long.
Cyanastrum has a corm that lacks a protective tunic. The leaf and the inflorescence emerge from different corm-scales, and are present at different times. The leaf has a short stalk, is basal and is usually single. The inflorescence is a raceme, often with no bracts, the tepals are blue and the flowers have parts in sixes.
Each stem bears an inflorescence of up to six clustered flowers. The pointed bracts at the base of the inflorescence are often over a centimeter long, longer the flower cluster itself, and are somewhat leaflike, giving the species its common name. Each flower has pointed outer tepals and thinner, shorter, oval-shaped inner tepals. There are three stamens.
The petiole margined and 2–5 mm long. The complete flower head of a plant including stems, stalks, bracts, and flowers, inflorescence, is short only about 1–2 cm long axillary. Cymose, definite inflorescence, with a single terminal female flower and several lateral male flowers. The bract, modified leaf, is triangular and 1–2 mm long.
The staminate inflorescences are panicles consisting of several erect catkins. The pistillate inflorescence is a terminal spike, which may be separate from the staminate inflorescence, or may be part of an androgynous panicle. The staminate inflorescences have an odor compared to the gardenia. The fruit is an oval nut, twice as long as wide, with a bitter meat.
Young parts of the plant, such as developing pitchers, are covered in a dense indumentum. However, most hairs are caducous and mature parts are virtually glabrous. An exception to this are the hairs on the ovary and some other parts of the inflorescence, which may be persistent. The stem, inflorescence and tendrils are characteristically purplish-red in most plants.
Schoenus crassus is a robust species, with plants usually having stiff, upright leaves. Other notable morphological characters include its firm and thickened primary inflorescence bracts, prophylls and prophyll mucros. In addition, this species has aristate spikelets. Schoenus crassus closely resembles Schoenus compactus, but the former species has a more elongate flowering head (inflorescence) compared to that of the latter.
Lomatium repostum is a spreading perennial herb growing up to half a meter long from a slender taproot. There is generally no stem, the leaves and inflorescence emerging at ground level. The leaf blades are made up of sharp-toothed oval leaflets each up to 6 centimeters long. The inflorescence is an umbel of yellowish-green to purplish flowers.
Lomatium rigidum is a perennial herb growing up to about half a meter-1.5 feet tall from a large taproot. There is generally no stem, the leaves and inflorescence emerging at ground level. The hairless gray-green leaf blades are made up of several sharp-toothed, fleshy segments. The inflorescence is a webbed umbel of tiny yellow flowers.
The stems are three-angled and narrow at the middle. Sheathing leaves occur at the stem bases as well as higher up the stems. The inflorescence occurs at the end of the stem, with small additional ones growing from leaf axils. The inflorescence consists of several clusters of many spikelets wrapped at the bases in a leaflike bract.
Dudleya greenei grows from a small, thick caudex a few centimeters wide and produces rosettes of fleshy, pointed leaves up to 11 centimeters long. The inflorescence is borne on an erect peduncle up to 40 centimeters tall. The peduncle and foliage are variably green and pink. The inflorescence branches at the top and holds many fleshy yellowish flowers.
The inflorescence appear in leaf axils with a barely discernible stalk. Each flower having a stalk long, covered in long soft white hairs. The bracts surrounding the flower heads are egg-shaped, very concave with flat longish hairs up to long. Each inflorescence has 20-26 unscented creamy-white flowers turning a deep pink with age.
Stems can reach a height of 40 cm (16 inches). Leaves and stems tend to be hairless toward the bottom, finely hairy above, and bristly in the inflorescence. Leaves are narrowly lanceolate, tapering gradually toward the tip. The inflorescence has 5-12 flowers, the flowers greenish-yellow each with a greenish-yellow to cream-colored bract below.
Astragalus malacus is perennial herb growing upright to a maximum height near 40 centimeters. Its leaves are up to 15 centimeters long and are made up of many oval-shaped leaflets. The inflorescence bears up to 35 magenta flowers, each up to 2 centimeters long. Stem, leaves, inflorescence, and sepals are coated in long, white hairs.
Inflorescence are erect and sometimes from old wood, they contain 10–16 flowers with simple rachis that are long. The inflorescence is glabrous or appressed-pubescent with pedicels approximately long. The fruit are formed in an obliquely obovate shape, long and wide. The fruit are black-pusticulate with a toothed crest found on either side of suture.
Typha shuttleworthii is very similar to T. latifolia and has long been considered conspecific with that species. More recent authors have, however, regarded it as a separate species. It differs from T. latifolia in that the male inflorescence is less than half the length of the female inflorescence, as well as having shorter anthers, smaller seeds, and narrower leaves.
Group of plants Inflorescence Orchis purpurea reaches on average of height. The leaves are broad and oblong-lanceolate, forming a rosette about the base of the plant and surrounding the flower spike. They are fleshy and bright green, and can be up to 15 cm long. The inflorescence is densely covered with up to 50 flowers.
Plants with narrower leaves generally grow in drier situations, whereas the broad-leaf form in wetter cooler locations. Leaves have 3-9 longitudinal veins radiating from the base. Numerous woody stems grow from a rootstock and form a clump, rarely branched below the inflorescence. The inflorescence is a slender raceme, long with 25–70 flowers per stem.
The leaves are usually longer than the culms and often curly at the apex and have a width of around . It blooms between April to November producing brown-red flowers. The head-like or simple inflorescence has one to four branches that in length. Each inflorescence is loosely or densely clustered with a globose shape and around in diameter.
It is a perennial herb forming generally two or more basal rosettes of thick, spoon- shaped leaves each a few centimeters long. The inflorescence arises from the rosette, a dense, spherical umbel of rounded sepals and four small petals. C. umbellata usually has only one inflorescence per basal rosette; the related Cistanthe monosperma generally has more than one.
The male and female feeding behaviour are different from one another. On one hand, the male feeds quickly at an inflorescence and then often flies up to 2m before feeding again. Feeding usually alternates with basking, courtship, etc. On the other hand, the female takes more time to feed and flies directly to the nearest inflorescence to feed further.
Inflorescence scapose, with bracts subtending each flower. Flowers actinomorphic, bisexual, solitary or in pseudoumbels. Sepals 3, persistent. Petals 3, white or yellow.
Dacryodes laxa is a tree in the family Burseraceae. The specific epithet ' is from the Latin meaning "loose", referring to the inflorescence.
The inflorescence is of racemes or panicles up to long, with a purple corolla that has white spots on the upper lip.
The inflorescence sometimes has two inflated whitish bracts alongside the flower. The seeds remain dormant in the soil during the dry season.
The inflorescence is an open array of spikelets generally green to purple-tinted in color. It flowers in late summer and fall.
Chisocheton patens is a tree in the family Meliaceae. The specific epithet ' is from the Latin meaning "spreading", referring to the inflorescence.
The inflorescence is a narrow array of thin branches bearing many tiny pointed or awned hairy spikelets each a few millimeters long.
The genus differs from the closely related Alloplectus in having an erect umbellate inflorescence and berries. The type species is C. capitatus.
The inflorescence is an open array of clustered bright blue, bell- shaped flowers up to a centimeter wide at the lobed mouths.
150px A thyrse is a type of inflorescence in which the main axis grows indeterminately, and the subaxes (branches) have determinate growth.
Catenospegazzinia elegans is a species of sac fungi. The holotype was found on dead inflorescence stalk of Xanthorrhoea preissii, in Western Australia.
The male inflorescence is about 8.6 cm long. The male flower is actinomorphic. Its floral peduncle averages at .95 cm in length.
The inflorescence is an umbel of white flowers.Forbes, R. Sium latifolium – greater water-parsnip. Northern Ireland Priority Species. National Museums Northern Ireland.
The inflorescence of the plant, or the collections of flowers, are composed of long section of spikelets largely concealed by long hairs.
The stem is surrounded by tapering leaves with blue-green bases. The inflorescence is a bundle of several clusters of brown flowers.
Apocryptophagus wasps are however gall forming non-pollinators. Some differences in Apocrypta behaviour and morphology reflect the variety in fig inflorescence morphology.
The inflorescence is a dense cluster of urn-shaped manzanita flowers. The fruit is a sticky, bristly drupe about 7 centimeters wide.
The inflorescence is a small cluster of blue or purple flowers. The fruit is a horned capsule about half a centimeter wide.
The inflorescence is a small cluster of many bright blue flowers. The fruit is a lobed, crested capsule about 4 millimeters wide.
The inflorescence is a pinkish violet flower surrounded by pairs of large, heart-shaped, green bracts, usually occurring in groups of 3.
The inflorescence is a tiny cluster of white-edged thin sepals and two white petals, each no more than a millimeter long.
The inflorescence is a cluster of many flowers surrounded by leaflike bracts. The flowers are pale blue and about a centimeter long.
Flowers show raceme inflorescence. Fruit is a single-seeded drupe. The tree is known as bo kera/mal kera in Sinhala language.
The majority of the characteristics of the species are lost in herbaria specimens, especially in the congested inflorescence of the scapeless taxa.
Illustration of Epidendrum secundum showing a secund inflorescence, from: Nikolaus Joseph, Freiherr von Jacquin (!793): Selectarum stirpium Americanarum historia Although the Linnaean binomial "Epidendrum secundum" is well established by Jacquin's publication in his Enumeratio (1760) and Selectarum (1763), the seeming inappropriateness of his word choice has long been noted, not only by Dressler (1975) but also by Cogniaux in Flora brasiliensis, with the listing "Epidendrum secundum (sed floribus non secundis) Jacq." Unlike the illustration in Selectarum, the inflorescence of this taxon is not secund, that is, the flowers are not all on one side of the inflorescence, are not all in one plane, nor is the plant in any way "lop sided." Rather the flowers surround the central stem of the inflorescence in a cylindrical manner, producing a highly congested raceme.
The inflorescence is a minute, threadlike umbel of tiny greenish white to maroon flowers each yielding a spherical fruit about a millimeter wide.
Heuchera hirsutissima is a rhizomatous perennial herb with small, lobed, rounded leaves. It produces an erect, hairy inflorescence which bears light pink flowers.
The inflorescence is a dense panicle occupying the upper half of the stem. Flowering occurs in July and August.Rumex orthoneurus. The Nature Conservancy.
Classen-Bockhoff R, Bull-Hereñu K. 2013. Towards an ontogenetic understanding of inflorescence diversity. Annals of Botany 112: 1523–1542. Carlquist S. 2003.
The stems grow up to 27 centimeters long and are lined with threadlike leaves. The short inflorescence bears spikelets under a centimeter long.
The inflorescence is a branching, spreading panicle up to 35 centimeters long bearing oval-shaped spikelets coated in downy white or silvery hairs.
The inflorescence arises on an erect peduncle up to 20 centimeters tall. An array of branches bear several flowers with small white petals.
The inflorescence is a length of bristly developing fruits tipped with open flowers with five-lobed white corollas just a few millimeters wide.
They are linear to lance-like in shape, tapering to a point. The inflorescence are characteristically T-shaped, with two (rarely three) racemes.
The inflorescence is a long raceme of flowers with six cream-white tepals. The fruit is a capsule.Xerophyllum asphodeloides. Flora of North America.
The flowers are borne in an open, branching inflorescence with leaflike bracts. The fruit is a spherical drupe up to 1.5 centimeters wide.
Dysoxylum brachybotrys is a tree in the family Meliaceae. The specific epithet ' is from the Greek meaning "short bunch", referring to the inflorescence.
The spikelets have awns up to 3 centimeters long. Spikelets low on the inflorescence often stay wrapped in sheaths and do not bloom.
Hakea incrassata inflorescence Hakea incrassata, commonly known as marble hakea, is a shrub in the family Proteacea and is endemic to Western Australia.
The erect inflorescence has a few branches each holding flat green spikelets. This is an important forage grass for livestock in some areas.
Adzuki flowers are papilionaceous and bright yellow. The inflorescence is an axillary false raceme consisting of six to ten (two to twenty) flowers.
The fruit is a hairy achene. The inflorescence are a food source for adult Lepidoptera, although they may not be the principal pollinators .
The inflorescence is an elongated cluster of many pale pink, hairy flowers with oval or somewhat triangular petals about half a centimeter long.
The inflorescence is an open or rounded cyme of five- petalled white flowers. The fruit is a toothed capsule containing several reddish seeds.
The inflorescence is a raceme atop the stem filled loosely with pink snapdragon flowers. Each flower is between one and two centimeters long.
The inflorescence is a small cluster of pale to bright blue flowers. The fruit is a horned capsule about half a centimeter long.
The inflorescence is usually narrow and thin. Coastal roadsides in Mendocino County, California can have populations, often receiving fog drip under Eucalyptus stands.
The inflorescence is an open array of spikelets, the lower ones drooping or nodding. The spikelets are flattened and usually hairy or downy.
The erect inflorescence bears several white mustardlike flowers. The fruit is a twisted, hairy, lance-shaped silique no longer than about a centimeter.
The inflorescence is in the form of a panicle. The flowers have separated triangular stigmas with fringes (fimbriate) borne on long divided styles.
The inflorescence is scapose, the single stem or scape bearing either a solitary flower or forming an umbel with up to 20 blooms.
Several of a mass of hundreds of such flowers on the inflorescence of Hesperoyucca whipplei It produces a stemless cluster of long, rigid leaves which end in a sharp point. The leaves are 20–90 cm (rarely to 125 cm) long and 0.7–2 cm wide, and gray-green in color. The leaf edges are finely saw- toothed. The single inflorescence grows extremely fast, and reaches 0.9–3 m tall, bearing hundreds of elliptical (bell shaped) white to purplish flowers 3 cm diameter on a densely branched panicle up to 70 cm broad, covering the upper half of the inflorescence.
Titan arum (Amorphophallus titanum), also known as the "corpse flower", is a flowering plant with the largest unbranched inflorescence in the world. The titan arum's inflorescence is not as large as that of the talipot palm, Corypha umbraculifera, but the inflorescence of the talipot palm is branched rather than unbranched. It is endemic flower of Sumatra, Java and bali - Indonesia. The titan arum is characterized as a carrion flower, and is also known as the corpse flower or corpse plant (Indonesian: bunga bangkai – bunga means flower, while bangkai can be translated as corpse, cadaver, or carrion).
Therefore, dead insects are frequently found within the inflorescence, when opened, sometimes leading the finder to believe it is a carnivorous plant – but that is not the case. No digestive enzymes or similar components are present; and in fact, once pollinated, the entire inflorescence starts withering except the central part, from which the berries later emerge. pp. 35-40 Pollination-wise, the species of Arum can be split into two (or three) distinct groups. The "cryptic" species have the inflorescence on a relatively short stalk, and the odour released during the thermogenesis is recognizable to the human nose as distinctively faecal.
The developing inflorescence is protected in a woody spathe, 60–180 cm in total length, which is usually hairless but may rarely be densely pruinose (covered in waxy flakes) or tomentose (furry); the spathe has a swollen part at the end 33–150 cm long and 6–16 cm wide, and ends in a sharp apex (tip). The inflorescence is branched to the first order. The rachis of the inflorescence is 20–104 cm long and has 35-141 rachillae (flowering branches) 15–132 cm in length. The flowers may be coloured yellow, reddish-orange, purple, yellow & purple, or greenish-yellow.
O. lebaense's bulbs, long leaves; and short, white, cone-shaped inflorescence grow pendent. This is the main characteristic which sets O. lebaense apart from other Ornithogalum species. Each plant has four or five semi-succulent leaves that curve in a spiral, and one or two inflorescences. The inflorescence is usually between 200 mm and 300 mm long, with clearly visible bracts.
Salvia barrelieri is a perennial found in northern Africa, Morocco, Tunisia, Algeria, and southwestern Spain, usually between the elevations of 500–1200 meters. It grows 1–2 meters tall, with large, wavy, gray-green leaves. The inflorescence is a verticillaster (See Inflorescence) and can grow nearly one meter tall, with flowers of light lavender or sky blue blooming all at the same time.
The inflorescence comprises a single, terminal, male (staminate) spike, and 2–4 lateral female (pistillate) spikes. The spikes are clustered together, and the whole inflorescence is long. The female spikes are long, ovoid or approaching spherical, and contains 5–15 flowers. The female spikes are attached directly to the stem, and each is subtended by a bract which does not form a sheath.
The inflorescence is a raceme of up to 50 flowers which are cream colored and sometimes tinted with light purple. Each flower is long including its tubular base of sepals. The fruit is a laterally compressed, slightly inflated legume pod up to long which dries to a papery texture. The fruits hang in bunches where they develop from the inflorescence.
Systematic Botany 31(1), 151-59. They produce a basal rosette of leaves and often lack a true stem, instead sending up a scape, a flowering stalk topped with an inflorescence. The inflorescence is usually made up of just one flower, but a large plant may produce several flowers in a raceme. The petals are white, yellow, orange, or lavender.
The lower branches may be woody, the upper hairless and waxy, and the inflorescence glandular. Most of the leaves are basal on the plant, rounded or oval, and up to about 4 centimeters long. The inflorescence produces purple- blue tubular flowers roughly 2 centimeters long. The flower has a glandular outer surface, a coat of hairs inside, and a hairless staminode.
The inflorescence consists of a main axis—the peduncle and the rachis—and a series of smaller branches, the rachillae. The rachillae, which bear the flowers, emerge from the rachis. The peduncle is the main stalk, connecting the rachis with the stem. The peduncle, the main stalk of the inflorescence, is no more than long and up to in diameter.
The inflorescence is up to 8 centimeters long and densely packed with pale pink to bright magenta flowers. Each flower is just under a centimeter wide and has a short throat spreading into a four-lobed corolla. Two very long stamens protrude from the throat of each flower, giving the inflorescence a whiskery look. The fruit is a capsule containing flat, smooth seeds.
Lomatium piperi is a perennial herb growing up to about 25 centimeters long from a spherical tuber no more than a centimeter wide. There is generally no stem, the leaves and inflorescence emerging at ground level. The leaf blades are divided into segments which are subdivided into narrow, flat lobes. The inflorescence is an umbel of white flowers with dark anthers.
Tripsacum dactyloides has separate female and male flowers on the same individual making it a monoecious plant. The inflorescence of the terminal axillary bud is long. The type of inflorescence is usually a single raceme or a panicle with a combination of two to three unisexual single racemes. Fruits: The seed-producing season of the grass is from June to September.
The stems are three-angled and narrow at the middle. Sheathing leaves occur at the stem bases as well as higher up the stems. The inflorescence occurs at the end of the stem, with small additional ones growing from the uppermost leaf axial. The inflorescence consists of several clusters of many spikelets wrapped at the bases in a leaflike bract.
The inflorescence of the herb is forty-flowered and arises from one to three nodes, with the ascending or horizontal flowering branches arising from up to six nodes. The lax inflorescence is predominantly cylindrical to subcorymbiform. The pedicels are long and the lanceolate, entire bracts and bracteoles are long. The star- shaped flowers are wide and are ellipsoid and obtuse while in bud.
True sago palm is a suckering (multiple-stemmed) palm, each stem only flowering once (hapaxanthic) with a large upright terminal inflorescence. A stem grows 7–25 m tall before it ends in an inflorescence. Before flowering, a stem bears about 20 pinnate leaves up to 10 m long. Each leaf has about 150–180 leaflets up to 175 cm long.
Collospermum hastatum The Asteliaceae is a family of two to four genera of plants found in the Southern Hemisphere. They are more or less rhizomatous, with spiral leaves and an inflorescence that may form a raceme or a spike. There are large bracts at the base of the inflorescence. The individual flowers are small, with tepals joined at the base.
The leaf margin is coarse, prickly serrated. The underside and the upper side of the leaf are only covered with gray when pressed on the lower half. For Puya species, an inflorescence is formed after relatively few years. The upright, strong inflorescence stem has a length of 90 centimeters and a round cross-section with a diameter of about 1 centimeter.
Castilleja lemmonii is a perennial herb 10 to 20 centimeters tall coated in glandular hairs. The leaves are 2 to 4 centimeters long and linear to narrowly lance-shaped. Closeup of Castilleja lemmonii inflorescence, pink bracts & small yellow, stamen-tipped flowers The inflorescence is made up of many purple- or pink- tipped greenish bracts. Between the bracts appear small yellowish flowers.
The inflorescence is a short, erect array of many small flowers with yellow petals. The specific epithet spathulifolium refers to the spade-shaped leaves.
The stems branch into an inflorescence studded with clusters of small yellowish flowers.Eriogonum visheri. Flora of North America. Flowering occurs in June through September.
The inflorescence is spiny, especially when in fruit. The fruit is a spherical, woolly bur about half a centimeter long covered in hooked spines.
The inflorescence branches and holds up to 25 knobby flowers on each branch. The flower has yellowish petals within its pink-tinged green sepals.
Lepidosperma squamatum is herbaceous and grows in height. It is a tufted perennial, also growing rhizomatously. Its brownish inflorescence appears between March and November.
The leaf blades are divided and subdivided into a mass of overlapping threadlike to oval segments. The inflorescence is an umbel of yellow flowers.
The inflorescence is an erect raceme of flowers, each with four small pink petals. The fruit is a capsule up to 4 centimeters long.
Leontopodium nivale is grown in gardens for its interesting inflorescence and silver foliage. The plants are short lived and can be grown from seed.
The inflorescence is a spike with the tiny male and female flowers clustered together. The fruits are small globular capsules containing disc-shaped seeds.
The inflorescence bears up 12 pinkish yellow pealike flowers each a centimeter long or more. The fruit is a slender, bent, beaked legume pod.
Perennial, very variable. Leaves ciliate at base and scabrous at margin. Inflorescence loose, more or less branching. Scales of calyx pale, membranous, briefly aristate.
The inflorescence is a solitary flower or cluster of up to three, each flower with five yellow petals up to 2 centimeters in length.
Inflorescence is a terminal tetragonal spike. The flowers are blue-violet or purple-white, 2.5–3 cm long. They bloom from June to August.
Leaves are simple and 2-lobed. Forked tendrils are usually present. Inflorescence is a lateral raceme. Flowers are yellow, bisexual, heterostylous, with 5 petals.
The inflorescence bears several white or green-tinged flowers with tubular throats up to 4 centimeters long, their bases enclosed in green-striped sepals.
It is interesting to note that there is no discontinuity in the phyllotactic pattern of the flowers between the different zones of the inflorescence.
The inflorescence at the tip of the stem is a cyme of a few flowers, each with usually five yellow petals under a centimeter long.
Lithocarpus dasystachyus is a tree in the beech family Fagaceae. The specific epithet ' is from the Greek meaning "thickly hairy spike", referring to the inflorescence.
The inflorescence produces a cluster of several rounded flower spikes. The pistillate flowers are covered in scales which are brown with green, three-veined centers.
The shiny leaf blades are up to 5 centimeters long. The inflorescence is a catkin. The species is dioecious. Flowering occurs in May and June.
Melica harfordii is a perennial bunchgrass growing up to in maximum height. The inflorescence is a narrow series of spikelets tipped with nearly invisible awns.
The inflorescence is a pendulous, two-part head of small flowers, which is followed by long, dangling pods each containing up to twenty-five seeds.
The inflorescence grows well above the leaves and is long. The yellow corolla is . The plant blooms in May and June and is a hemicryptophyte.
The plant is monoecious with both sexes in each flower. The flowers have no scent. The bracts subtending the inflorescence are deep pink in colour.
Inflorescences are organized on indistinct peduncles. Each inflorescence has a single flower. Each flower is on a densely hairy pedicel 11-26 millimeters in length.
The inflorescence emerges at ground level, bearing either male or female flowers, in the latter forming scaly, red fruit with one or occasionally two seeds.
The inflorescence bears one or more flowers with usually four tiny bright yellow petals. The fruit is a flat capsule up to a centimeter long.
The inflorescence contains many crowded cream or pink flowers. The fruit is about a centimeter long. There are several subspecies of this plant. The ssp.
The narrow leaves are flat and edged with small, sharp teeth. The inflorescence is a large panicle of spikelets yielding oval-shaped, purplish-brown fruits.
The leaves have oval blades lined with blunt teeth borne on long petioles. The inflorescence arises on a hairy peduncle, the flowers bearing white petals.
It can be distinguished from the similar-looking Phytolacca acinosa by its fused carpels, and from Phytolacca americana by its more dense and erect inflorescence.
The inflorescence is an open array of thin branches bearing rough-haired, flattened, lance-shaped spikelets. The spikelets may be greenish to purple in color.
The leaves sheath the stems and have short, narrow blades. The inflorescence is a cluster of several spikelets accompanied by a long, stiff, stemlike bract.
The plant erects tall peduncles which support the flowers. The peduncles and umbels are brownish and the small flowers within the crinkly inflorescence are white.
This species grows up to half a meter tall. The inflorescence is a raceme of 4 to 10 large, white flowers.Impatiens wilsoni. Flora of China.
Phalaris angusta is an annual grass reaching as much as 2.5 meters tall. The inflorescence is a narrow cylindrical spike of rough-haired, pointed spikelets.
The herbage of the inflorescence is coated in black hairs. The fruit is a tiny rounded or oval legume pod just a few millimeters long.
The inflorescence is a head with 5 square-tipped, petal-like ray flowers and sepal-like phyllaries. Fruits are seeds attached to parachute-like pappi.
Mastixia trichotoma is a tree in the family Nyssaceae. The specific epithet ' is from the Greek meaning "three parts", referring to the three-branched inflorescence.
The inflorescence is a compound umbel of many spherical clusters of small white flowers. These yield ribbed, oblong-shaped fruits 3 to 6 millimeters long.
Inflorescence is up to 10 cm (4 inches) long with densely hairy spikelet bracts and fascicles.Alexeev, Eugeniy Borisovich. Novosti Sistematiki Vysshchikh Rastenii 22: 28. 1985.
The inflorescence is a series of single-spikelet nodes a few centimeters long, each spikelet with an outward-curved awn up to 2.5 centimeters long.
The inflorescence is a cluster of brown, pale green, or straw-colored flowers accompanied by one bract which appears as an extension of the stem.
The inflorescence (or blooms), are produced in April, or June, they are fan-shaped and contains two or three white flowers, with a purple mark.
The inflorescence holds a solitary white flower which is sometimes tinted with pink or yellow. The flower is 2 to 4 centimeters wide when open.
The cylindrical inflorescence is up to 12 centimeters long, each spikelet made up of one strongly beaked fertile floret and one or two sterile florets.
The inflorescence is up to long, with each hairy spikelet bearing an awn up to 4 or 5 centimeters long. The awn is kinked twice.
They may become curly with age.Aristida purpurascens. USDA NRCS Plant Fact Sheet. The panicle-shaped inflorescence has branches appressed to the stem, making it narrow.
Pollination bags are designed to fit well over the inflorescence or individual flowers of a plant type. The size, shape and strength of bag should ensure that there is no contact with flowers to avoid development of diseases and physical hindrances in seed development. The size of bag will vary with the size of inflorescence to be covered. Pollination bags may be 2D or 3D.
Carex simulata produces sharply triangular stems up to 80 centimeters tall from a long, coarse, dark brown rhizome. The inflorescence is dense and rounded to open and long, containing several flower spikes. The plant is generally dioecious, with individual plants bearing male or female flowers, but not both. The male, staminate inflorescence is usually longer and more narrow than the oval-shaped female, pistillate spike.
The inflorescence arises on an erect stem up to 40 or 45 centimeters tall which is whitish and hairy when new and turns reddish as it ages. The inflorescence itself is a cluster of up to 35 flowers a few centimeters wide. The woolly flowers are pink-tinged when in bud and turn bright white when open. The stamens are tipped with yellow or pink anthers.
Eriogonum cedrorum is a mat-forming perennial herb growing up to half a meter wide with hairy or woolly herbage. It has a woody taproot and caudex unit covered in rosettes of leaves each up to 1.5 centimeters long by 1 wide. The inflorescence arises on an erect stem up to 8 centimeters. The inflorescence itself is a cluster of yellow flowers that quickly turn dark red.
Spinifex sericeus has branched stolons and rhizomes extending up to . The leaves have a ligule of a rim of dense hairs; the blades are flat and densely silky. The male inflorescence is an orange-brown terminal cluster of spiky racemes subtended by silky bracts. The female inflorescence detaches at maturity, a globose seed head of sessile racemes up to 20 cm in diameter which becomes a tumbleweed.
Atop the stem is a showy inflorescence of many bright yellow flowers. Each flower has oblong petals around a cluster of long stamens tipped with knobby anthers. As the inflorescence lengthens at the top of the stem, flowers that have opened and been pollinated drop their petals and the ovary develops into a fruit. The fruits are capsules several centimeters long containing many seeds.
Poa confinis is a perennial grass growing in small tufts with rhizomes and stolons, reaching up to about 30 centimeters tall. The narrow leaves are firm to stiff and sometimes folded or rolled along the edges. The inflorescence is a small, rough-haired, light brown cluster of spikelets. The plant is dioecious, with male and female individuals producing different types of inflorescence, the types similar in appearance.
The up to 40 cm tall inflorescence produces one to three flowers at its apex that are typically 15–20 mm long and are the largest of the yellow-flowered species. Each inflorescence can produce up to a total of eleven flowers. In its natural habitat, G. aurea can be found flowering year-round. The flowers and the scapes are densely covered in glandular trichomes.
Lomatium mohavense is a hairy gray-green perennial herb growing 10 to 40 centimeters tall from an elongated taproot. There is generally no stem, the erect or spreading leaves and inflorescence emerging from ground level. The leaves may approach 20 centimeters long, their blades intricately divided and subdivided into crowded clusters of tiny segments. The inflorescence is an umbel of yellow to brownish to dark purple flowers.
Lomatium ravenii is a hairy, gray-green perennial herb growing 5 to 40 centimeters long from a taproot and tuber unit. There is generally no stem, the leaves and inflorescence emerging at ground level. The leaf blades are divided into segments which are subdivided into smaller oval or knoblike segments. The inflorescence is a hairy umbel of white or purple-tinged flowers with dark anthers.
Dead leaves are marcescent in juvenile palms, but abscise, naturally fall off the tree, neatly in adults. The inflorescence is infrafoliar and surrounded by a long, leathery spathe, which curls up on itself after abscission (due to drying out). The inflorescence stalk is long and elliptic in cross-section. The rachis is very short, long and bearing about 30–50 crowded, spirally arranged rachillae.
The lid or operculum is orbicular and has a distinctive glandular crest on its underside. An unbranched spur is inserted near the base of the lid. An intermediate pitcher Nepenthes faizaliana has a racemose inflorescence. The female inflorescence of this species has not been formally described. In male inflorescences, the peduncle is up to 17 cm long, while the axis reaches 40 cm in length.
Astragalus didymocarpus is a slender, hairy annual herb growing erect to about tall, drooping, or flat on the ground in a spreading clump. The leaves are up to long and are made up of narrow to oblong leaflets. The inflorescence is a cluster of up to 30 purple-tinted white flowers, each under long. The inflorescence is covered in long black and white hairs.
Namophila urotepala grows from an underground bulb, which has a dark brown papery tunic. The bulb produces only two somewhat succulent leaves which spread out on the ground on either side. The flowers are produced in a several-flowered raceme borne on a very short stem so that the inflorescence is at ground level. At the top of the inflorescence is a tuft of bracts.
It has a short warty trunk and thick branches. The upright and terminal inflorescences which occur on short thickened stems off the branches are grey in bud and up to 25 cm x 12 cm in size. The yellow styles emerge in a spiral at the bottom of the inflorescence and gradually cover the whole inflorescence. Lorikeets and other birds are attracted to the nectar.
The mostly bisexual flowers are immersed in the inflorescence axis and more or less connate to each other, to the bract, and to the axis. The inconspicuously three-lobed perianth consists of three connate tepals. There are one ore two (rarely three) stamens shortly exserting the flower, and an ovary with two stigmas. The fruit remains enclosed in the inflorescence axis, the fruit wall (pericarp) is membranous.
It can become abundant, practically covering the surface of the water. It is a perennial herb producing a floating stem with long, narrow, flattened leaves which can be quite long, sometimes reaching over two meters. It is monoecious, individual plants bearing both male and female inflorescences. These are spherical, the male inflorescence a ball of stamens and the female inflorescence a ball of developing fruits.
Detail of the florets and bracts of a flowering orange tulip ginger Glossy, overlapping bracts form a terminal inflorescence, that is spike-shaped to ovoid. The bracts are red to orange, usually becoming more orange at the apex, which curves outward. The inflorescence is quite variable in size, ranging from long and cm broad. During flowering, small, hermaphroditic yellow or orange tubular florets emerge among the bracts.
Morphologically, it is the modified part of the shoot of seed plants where flowers are formed. The modifications can involve the length and the nature of the internodes and the phyllotaxis, as well as variations in the proportions, compressions, swellings, adnations, connations and reduction of main and secondary axes. One can also define an inflorescence as the reproductive portion of a plant that bears a cluster of flowers in a specific pattern. The stem holding the whole inflorescence is called a peduncle and the major axis (incorrectly referred to as the main stem) holding the flowers or more branches within the inflorescence is called the rachis.
Inflorescence from Philodendron cannifolium When philodendrons are ready to reproduce, they will produce an inflorescence which consists of a leaf-like hood called a spathe within which is enclosed a tube- like structure called a spadix. Depending on the species, a single inflorescence can be produced or a cluster of up to 11 inflorescences can be produced at a single time on short peduncles. The spathe tends to be waxy and is usually bicolored. In some philodendrons, the colour of the base of the spathe contrasts in colour with the upper part, and in others, the inner and outer surfaces of the spathe differ in coloration.
Pupation takes place on the inflorescence stalks or on nearby blades of grass. The pupa is light green at first, changing to yellowish tan and brown.
The inflorescence is an open array of star-shaped spikes of flowers covered with gold scales. The fruit is coated in a toothed, red-tipped perigynium.
The inflorescence is a small array of white flowers with lobes just under a centimetre long. They are sometimes lavender-tinted and open in the evening.
This plant does not have bulblets in the inflorescence. The flowers mature into spherical crested fruits which later split open to reveal the dark shiny seeds.
The inflorescence is a loose umbel of tiny flowers each made up of whitish, petal-like sepals less than 2 millimeters long, and no true petals.
The inflorescence is a spike up to about 12 cm long made up of spikelets up to about 3 cm long each, usually tipped with awns.
The inflorescence arises on a stout, hairy peduncle up to 35 centimeters tall. White-petaled flowers occur in a cluster or dense array at the top.
The serrated leaves are up to a meter long. The inflorescence is a plume-like panicle of spikelets covered in white or pale-colored silky hairs.
The inflorescence is a compound cyme of tiny flowers. H. mutilum subsp. mutilum and subsp. boreale have a diploid number of 16, and H. mutilum subsp.
They are coated in white hairs. The inflorescence is a dense cluster of tiny white flowers, each pointed corolla lobe just a millimeter long or so.
Inflorescence is branched 1-2 times with 2-4 buds borne on short peduncle. Petals are white and slightly hairy with style 2–3 mm long.
Carnivorous Plants in the tropics. They bear reduced fringed wings or ribs. Nepenthes mapuluensis has a racemose inflorescence. The peduncle is up to 7 cm long.
In this case, it refers to the inflorescence which is an umbel of triads, which is often a pair (see illustration on p 89 of Kuijt).
The nodding inflorescence produces flowers with yellow petals a few millimeters long with red markings near the bases. The fruit is a straight or coiling capsule.
The inflorescence is a row of bell-shaped white flowers each just under a centimeter long. The fruit is a capsule.Eubotrys racemosa. Flora of North America.
The pointed leaves are up to 4 centimeters long. The inflorescence is a short, coiling series of tiny white flowers each only about a millimeter wide.
The inflorescence is evenly lined with hanging involucres of flowers. The individual flowers are less than 2 millimeters wide and white to pink-tinged in color.
The inflorescence is a branching cyme bearing many clusters of flowers. The individual flowers are 1 to 2 millimeters wide and white or pink in color.
The inflorescence is a spherical flower head a few millimeters wide which resembles a tiny cotton boll since the flowers and maturing fruits are very woolly.
The inflorescence produces purple flowers. The plant grows in moist forest habitat. Threats to the species include degradation of this habitat by feral pigs and rodents.
The narrow linear leaves are up to 38 centimeters long by 1.5 wide. The inflorescence is a raceme of purple-pink flowers.Cyanea kuhihewa. The Nature Conservancy.
Different authors accept from four to 18 species in the genus. The inflorescence consists of large colourful sepal-like bracts which surround three simple waxy flowers.
The plant bears an inflorescence of two to eight pinkish purple pea flowers each up to two centimeters wide. The fruit is a dehiscent legume pod.
The flowers are orange-red (rarely yellow), glossy, and are born on 20–25 mm pedicels, on capitate or subcapitate racemes, on a branched inflorescence (panicle).
Inflorescence in racemes smaller than leaves. Perianth made of 6 petal-like yellow sepals, in diameter. Stamens ; anthers oval. Ovary topped by a thick sessile stigma.
The inflorescence is a cluster of many flowers surrounded by leaflike bracts with awl-shaped lobes. The flowers are white and under a centimeter in length.
The inflorescence is a dense, narrow, cylindrical tuft no longer than 5 centimeters in length, made up of small spikelets with hairlike tips and bent awns.
A rhipidium is a built partial inflorescence in which the prophyll of a lateral axis subtends a new lateral axis, each axis ending in a flower.
The upper portion of the plant makes up its inflorescence, which often has a flat top. The tiny clustered flowers are white to yellow or sometimes pinkish.
The inflorescence is a dense or open bundle of rounded or oval brown flower spikes. The fruit is coated in a veined perigynium with a white tip.
The genus Latin name (“campanula”), meaning small bell, refers to the bell-shape of the flower, while the specific epithet (“spicata”) refers to the spike-shaped inflorescence.
Adenodolichos paniculatus is a plant in the legume family Fabaceae, native to tropical Africa. The specific epithet means "with panicles", referring to the plant's many-branched inflorescence.
Specialised characters of T. rostratus include visual acuity for detecting the bright yellow inflorescence of Banksia attenuata. They have a typical lifespan between one and two years.
At the junction of the sheath and blade there is also small ligule, extending to 1–2 mm. The flower spike (inflorescence) is held within the leaves.
The shrub is of interest to the botanist because of its unique (within the genus) resting buds and the different types of inflorescence produced through the year.
The specific epithet brachiata is from the Latin meaning "branched", referring to the decussate inflorescence. O. brachiata is native to China, Thailand, Cambodia, Vietnam, Malaysia and Indonesia.
The hairy blades are borne in opposite pairs on the stem. The inflorescence at the tip of the stem produces deep blue flowers a few millimeters wide.
Dysoxylum pachyrhache is a tree in the family Meliaceae. The specific epithet ' is from the Greek meaning "thick axis", referring to the axis width of the inflorescence.
Within this group, it is closely related to Madagascan Aloe occidentalis (which can be distinguished by having longer leaves, shorter inflorescence, and longer perianths, than Aloe tormentorii).
Melochia umbellata is a species of flowering plant in the mallow family, Malvaceae. Its specific epithet comes from the Latin umbellatus (umbel-like), referring to the inflorescence.
The inflorescence is a solitary flower head with yellow to reddish disc florets. The fruit is a ribbed cypsela about one millimeter long with a large pappus.
The leaves may be thin and early- withering or somewhat fleshy and persistent. The inflorescence is a dense cluster of short branches bearing small, hairy-edged spikelets.
Flowering occurs in fall. The plant produces an inflorescence of several pinkish flowers on a tall peduncle. The fruit is a red-striped green or pink capsule.
The leaves are borne on petioles up to 10 centimeters long. The inflorescence is a spherical cluster of purplish or off-white flowers atop a long peduncle.
A variable species, usually a blue-green colour but sometimes reddish, especially in exposed positions. The inflorescence is branched, and the flowers reddish orange with yellow tips.
The only mature parts that retain an indumentum are the inflorescence and tendrils, which bear an inconspicuously puberulent covering of simple, black hairs of around 0.3 mm.
The inflorescence bears tubular flowers each up to 3.4 centimeters in length. The flowers are pale lavender to blue-purple and have yellowish hairs inside their mouths.
The waxy gray-green leaf blades are made up of several very small, sharp-toothed, fleshy segments. The inflorescence is a small umbel of tiny purple flowers.
The leaves are located around the stem bases, and are straight or curled. Old leaf sheaths become shreddy. The inflorescence is a spike up to long.Psathyrostachys juncea.
The inflorescence bears an umbel of yellowish, purplish, or white flowers. The fruit is a compressed, winged, round or oval disc up to about 2 centimeters long.
The leaf blades are divided and subdivided into narrow segments. Leaves higher on the stem are enclosed in sheaths. The inflorescence is an umbel of yellow flowers.
The inflorescence is a head of four to nine pale purple flowers, each just under long. The fruit is a bladdery legume pod which can exceed long.
Finally, the larvae lives in the inflorescence, feeding on the developing fruits. Larvae can be found from September. They overwinter as a larva before pupating in June.
V, Grasses. P. 368. The inflorescence is a spreading panicle with the lower parts drooping more than the upper. The spikelet is up to 6 cm long.
Basil grows a thick, central taproot. Its flowers are small and white, and grow from a central inflorescence that emerges from the central stem atop the plant.
The inflorescence atop each stem branch is a spike up to long containing many purple flowers. The fruit is a legume pod containing 1 or 2 seeds.
There are tiny bristlelike tendrils. The inflorescence bears two greenish-white pea flowers each up to a centimeter wide. The fruit is a hairless dehiscent legume pod.
The specific epithet spicatus (Latin "spiked") refers to its inflorescence. Habitat is forests from sea- level to altitude. C. spicatus is found in Borneo and the Philippines.
Under George's 1999 arrangement, B. epicas placement was as follows: Closeup of leaves, with inflorescence in early bud :Banksia ::B. subg. Banksia :::B. sect. Banksia ::::B. ser.
The inflorescence is a wide array of a few tubular flowers. Each is or long, coated in glandular hairs, and dark- veined pink or purple in color.
The terminal inflorescence contains numerous whitish or pale lilac lipped flowers with large shelf-like lower lips. The fruits contain four pitted seeds covered with white hairs.
The inflorescence has two or three pea flowers in varying shades of red, each up to 3 centimeters wide. The fruit is a hairless dehiscent legume pod.
The inflorescence bears small flowers with five pointed sepals and five oval white or pink petals. The fruit is a capsule containing shiny, sometimes iridescent, black seeds.
Inflorescences emerge from the leaf axils arranged alternately on the main stem. Oftentimes during development they puncture the epidermis at the base of the leaves. A single inflorescence typically carries only 2 or 3 flowers at a time, however more has been observed. Flowers may emerge from the tip of the inflorescence from spring through summer, and continue to do so for many years until the stem dries up.
These are articulated, basally conduplicate, ligulate sometimes with acute apex, thin and narrow, very malleable, light green colored. The inflorescence is erect or arching, shorter than the leaves and bares one to nine flowers sometimes showy, which open in quick sequence holding at least three of four opened at the same time. The inflorescence shoots among the foliar sheaths on the pseudobulbs bases. The flowers vary according to the species.
The upper surface of the petiole is glabrous, but the margins and lower surface possess hairs similar to those of the abaxial leaf surface. One or two racemose inflorescences are produced per plant and are usually long. Approximately 12 flowers are found on one inflorescence with each white or pink flower held on a 3–5 mm long pedicel. The scape, inflorescence, and sepals are sparsely covered in white hairs.
Nepenthes micramphora has a racemose inflorescence measuring up to 35 cm in length by 6 mm in width. The peduncle itself may be up to 8 cm long and 1 mm wide. Flowers are borne on one- flowered, non-bracteate pedicels (3–4 mm long), of which there are between 20 and 40 on the inflorescence. The ovate tepals measure up to 2.5 mm in length by 1.2 mm in width.
The leaf is hairless and when crushed gives off a lemon-ginger scent like other grasses in the genus Cymbopogon. The inflorescence of the plant, or the collections of flowers, are arranged on a long stem with clusters of short, nearly hairless branches which bend downwards when mature, giving the inflorescence a barbed- wire appearance. The spikelets are paired, one stalked the other unstalked. Flowering mostly spring to autumn.
N. papuana has a racemose inflorescence, while that of N. neoguineensis is a panicle or panicle-like raceme. Furthermore, the inflorescence of N. papuana usually bears only one-flowered pedicels, both in male and female plants. Those of N. neoguineensis can be up to four-flowered. The lamina of N. papuana has very distinct longitudinal veins and indistinct pinnate veins, whereas in N. neoguineensis the opposite is true.
Beggar-tick (Bidens comosa) Bracts that appear in a whorl subtending an inflorescence are collectively called an involucre. An involucre is a common feature beneath the inflorescences of many Apiaceae, Asteraceae, Dipsacaceae and Polygonaceae. Each flower in an inflorescence may have its own whorl of bracts, in this case called an involucel. In this case they may be called chaff, paleas, or receptacular bracts and are usually minute scales or bristles.
Its inflorescence is 90–120 cm long, usually with 3-7 branches (each 30–60 cm long). The inflorescence, pedicels, and erect flower buds are all salmon coloured. The flowers become paler yellow after opening. They have green tips and in habitat they are often frayed and torn from the tiny endemic gecko species which push their heads into the perianth tube to lick the nectar and thereby pollinate the plants.
The leaves grow in a dense basal clump at the ground. They are fat and fleshy and covered in a carpetlike coat of stiff, light colored branching hairs. The stem may be erect above the clump of leaves or its inflorescence may rest directly upon them. The spherical or club-shaped inflorescence may have up to 80 small yellow flowers packed densely in it, each petal about 5 millimeters wide.
The texture of the leaves may be cartilaginous, leathery or herbaceous. The flowers are at the end of one or several branching inflorescence stalks, that carry several bracts much smaller than the leaves, at least substending each of the branches. These inflorescence stalks may be roughly hairy to hairless, and round or angular in cross-section. The compounded inflorescences may be compact or loosely composed racemes, panicles or corymbs.
Flowers initially occur in clusters of 1–6 at intervals along the stem (scape) of the inflorescence. Each cluster is at the base of a bract, which ranges from in length, becoming smaller towards the end of the inflorescence. Most of the flowers which are produced initially die off, so that the inflorescences are relatively sparsely flowered. Individual flowers are greenish-white, borne on stalks (pedicels) some long.
This pampas grass, Cortaderia jubata, has long, thin, razor-edged leaves forming a large bunch grass tussock from which the eye-catching inflorescences arise. At the top of a stem several meters in height is an inflorescence of plumelike spikelets. These panicles are pink or purplish when new and they gradually turn cream or white. Each inflorescence is packed full of fruits which develop despite the plant's having never been fertilized.
N. papuana has a racemose inflorescence, while that of N. neoguineensis is a panicle or panicle-like raceme. Furthermore, the inflorescence of N. papuana usually bears only one-flowered pedicels, both in male and female plants. Those of N. neoguineensis can be up to four-flowered. The lamina of N. papuana has very distinct longitudinal veins and indistinct pinnate veins, whereas in N. neoguineensis the opposite is true.
The stems are round in cross-section, unlike those of sedges, which are typically somewhat triangular in cross-section. In Juncus section Juncotypus (formerly called Juncus subg. Genuini), which contains some of the most widespread and familiar species, the leaves are reduced to sheaths around the base of the stem and the bract subtending the inflorescence closely resembles a continuation of the stem, giving the appearance that the inflorescence is lateral.
It can exceed two meters in height, its inflorescence reaching 4 meters. The trunk is up to 60 centimeters in diameter. Leaves are borne in dense rosettes, each with up to 220 stiff linear leaves up to 140 centimeters long and 4 broad. It is dioecious, with separate male and female plants; the flowers are white, produced on the tall plume-like inflorescence that normally appears in late spring.
California Native Plant Society Rare Plant Profile This is a perennial herb growing an erect inflorescence from a mat of silvery, woolly- haired herbage, reaching maximum heights over half a meter. Each palmate leaf is made up of 6 to 9 leaflets up to 7.5 centimeters long. The inflorescence is a raceme of whorled flowers each just over a centimeter long. The flower is cream to pale brownish yellow in color.
Allotropa virgata has an underground stem (rhizome) with brittle roots. The scale-like leaves are along the striped peduncle with a raceme-like inflorescence. The peduncle is persistent after the seeds have been dispersed and tends to turn brown. The bracts of the inflorescence are less than 3 cm and the pedicels are not recurved. The individual flowers generally don’t have sepals but if they do, have 2 to 4.
The foliage is scabrid, crisped-villous or puberulent with yellow glandular hairs. Leaf margins are coarsely or double-serrate. The flowers are collected together into capitula (heads) that are densely corymbose, the inflorescence are usually 3 to 6 cm wide and rarely form large compound corymbose inflorescence that can be up to 20 cm wide. The involucre are campanulate shaped and 5–6 mm wide, composed of five flowers.
Utricularia densiflora is a carnivorous plant in the genus Utricularia and is endemic to Brazil. It is a hydrophytic herb that has stolons up to long. It produces inflorescences around long with the bracts and flowers arranged spirally around the inflorescence. The species epithet densiflora refers to the density of flowers that each plant produces, which typically ranges from 15 to 23 flowers congested near the top of the inflorescence.
Inflorescence and Corolla Differences Inflorescences can be acted on by sexual selection in many ways, and commonly include arrangement, number, and size. For example, male inflorescence in plants often produce more flowers than females . Furthermore, pollen export and ultimately paternity, often increases with flower number, even for plants with hermaphroditic flowers. Retention of older flowers with no pollinator rewards can lead to increased pollinator visitation rate and increased pollen removal.
The leaf is dark green and in this species the midrib is streaked with white. The netlike veining on the leaf is also white, but not as thick as the midrib stripes. The plant produces an erect inflorescence up to about 30 centimeters tall. The top of the inflorescence has many white orchid flowers which may all face the same direction on the stalk, or be spirally arranged about it.
Renanthera matutina is a monopodial epiphytic orchid that produces a long branched pendulous stem about long, bearing the inflorescence. The numerous flowers are pinkish-yellow, with red spots.
They are shrubs or small trees growing to tall. The leaves are simple, arranged in opposite pairs or whorls of three. The flowers form a dense globular inflorescence.
The inflorescence is a cyme of 2 to 5 flowers, each with 5 pointed green sepals and 5 rounded white petals. The fruit is a toothed black capsule.
Leaves are heart-shaped, up to 16 cm long. Inflorescence is a racemous thyrse.Gillespie, Lynn Judith. 1997. Omphalea (Euphorbiaceae) in Madagascar: a new species and a new combination.
The leaves are curved, canaliculate and a creamy, greenish-yellow khaki colour. The inflorescence is short, unbranching, and starts out horizontal. The flowers are orange with green tips.
The oval-shaped leaves are long and wide and form a rosette on the top of the plant. Each inflorescence contains three to eight trumpet-shaped white flowers.
The inflorescence is a compound raceme, the individual scented bisexual flowers having five, unequal creamy-white petals. These are followed by flattened oblong pods each containing one seed.
The small inflorescence grows up to 9 centimeters tall and bears several flowers with white petals tinged or veined with pink. The stamens have red or black anthers.
Parinari argenteo-sericea grows as a tree up to tall. The brown bark is lenticellate. The inflorescence is up to long. The ovoid fruits measure up to long.
Male inflorescence of Attalea sp. swarming with insects. Attalea sp. – MHNT Attalea species are monoecious—male and female flowers are separate, but are borne by the same plant.
The inflorescence is a cluster of flowers surrounded by five hairy greenish bracts tipped with hooked awns. The flower is about 2 millimeters wide and yellow in color.
The rarer, var. leucotheca, is known only from the San Jacinto and San Bernardino Mountains. It has a much more thickly woolly inflorescence than the more common variety.
The inflorescence is a compound umbel of many spherical clusters of small white flowers. These yield ribbed, round or oblong-shaped fruits each about half a centimeter long.
The inflorescence is an umbel of up to 25 white flowers with yellow anthers.Cirillo, Domenico Maria Leone. 1788. Plantarum Rariorum Regni Neapolitani 1: 13.Hickman, J. C. 1993.
The inflorescence bears flowers with pink petals just over a centimeter long and a protruding pistil. The fruit is a hairy, glandular capsule up to 4.5 centimeters long.
The inflorescence is a raceme of flowers with yellow-green sepals and no petals. It is the only Heuchera with six-parted flowers.Heuchera eastwoodiae. Flora of North America.
G. brachystylis grandis typically grows to a height of , has non-glaucous branchlets and simple leaves long and wide. It produces irregular red inflorescence from August to September.
The leaves are short, pointed, and somewhat hairy. The inflorescence is up to 3 centimeters long and one wide, flat and hairy with spikelets a few millimeters long.
The small gray-green leaves are usually lobed. The inflorescence is an array of several flower heads containing yellow ray and disc florets. The fruit is an achene.
The inflorescence is a long cluster of deep blue flowers, up to about 15 centimeters long. The fruit is a smooth, 3-lobed capsule a few millimeters long.
Tetramolopium rockii. The Nature Conservancy. This plant is a small, mat-forming shrub growing no more than about 10 centimeters tall. The inflorescence contains a single flower head.
The inflorescence is a cluster of a few several yellowish or green-tinged, star-shaped flowers with five petals. The fruit is a dry drupe containing one seed.
The leaves usually have an olive-green to brown colour. In the summer (November to December) Tulista pumila produces pink-white tubular flowers, on a tall thin inflorescence.
The leaves have three leaflets. The inflorescence is a terminal raceme of flowers. The flowers are yellow, sometimes fading orange or purple.Moteetee, A., & van Wyk, B. E. (2006).
The blade is borne on a long petiole, with upper leaves having larger petioles than basal. The inflorescence is a dense compound umbel of many small white flowers.
Inflorescence an erect terminal and lateral raceme, up to 30 cm long, 12–20-flowered. Pedicel c. 3–7 mm long. Bract minute; bracteoles 2, below the calyx.
Several inflorescences arise from the stem, often but not always from leaf axils. The inflorescence is a compound umbel of tiny flowers each with five pointed white petals.
The inflorescences last for two nights and are protogynous in some species (though not others (), changing from the pistillate phase that attracts pollinators on the night it opens, to a staminate phase on the second night, when pollen is shed. When the inflorescence opens, it produces heat and releases a sweet scent attracting its pollinators, dynastine beetles (Cyclocephala spp.). Dynastines arrive covered with pollen from another inflorescence and remain in the spathe tube for 24 hours, pollinating the pistillate flowers as they feed on the sterile area of the spadix. On the second night, they come out of the tube and walk over the staminate flowers, getting covered with pollen, and then flying to a recently opened inflorescence nearby. ().
The inflorescence is a short, erect array of one to many flowers with lance-shaped petals up to a centimeter long. The petals are yellow, sometimes with red veins.
One former species, esparto grass (Macrochloa tenacissima), is used for crafts and extensively in paper making. It is a coarse grass with inrolled leaves and a panicle patterened inflorescence.
The showy inflorescence is an umbel of several flowers with tubular yellow throats and flat magenta corollas with five jagged or notch-tipped lobes. The fruit is a capsule.
Compare with Papyrus Cyperus scapes. Contrast with peduncle of Agave In botany, a peduncle is a stem supporting an inflorescence, or, after fecundation, an infructescence.Shashtri, Varun. Dictionary of Botany.
Melica nitens. NatureServe. This perennial grass has short rhizomes and sometimes forms bunches. The stems grow up to 1.3 meters tall. The inflorescence is a branching panicle of spikelets.
The narrow leaves are mostly located on the lower third of the clumped stems. The inflorescence is a narrow, erect panicle with spikelets green, brownish, or purple in color.
The inflorescence is an open array of flowers, each blooming in an involucre of spiny bracts lined with awn-tipped teeth. The six- lobed flowers are white to pink.
It is a perennial bunchgrass which varies in maximum height from 10 to 90 centimeters. The inflorescence is a narrow panicle of V-shaped green and purple banded spikelets.
The inflorescence is a spike with interrupted clusters of 3 to 5 small, yellow-green to yellow-brown flowers. Flowering occurs in June and July.Sinadoxa corydalifolia. Flora of China.
Its fruits mature in the summer. It is similar to the closely related Cyperus echinatus, from which C. retrorsus can be distinguished by its cylindrical inflorescence and shorter stature.
The nodding inflorescence produces several flowers, each with white petals a few millimeters long and drying to dull red. The fruit is a capsule 3 to 5 centimeters long.
The sparse inflorescence is a wide, flat, open array of spikelets that break apart easily. The grain has a twisted tip and three awns up to 2 centimeters long.
The nodding inflorescence bears flowers with yellow petals each a few millimeters long. The fruit is a cylindrical capsule up to 2.5 centimeters long containing several dark-colored seeds.
The flower stalk grows 60 cm or more above the foliage, with pale yellow flowers in whorls of six or more that make an inflorescence 20–25 cm long.
The inflorescence has clusters of flower heads each up to about a centimeter long. Each contains white or off-white disc florets and usually a few white ray florets.
The inflorescence is a solitary flower with five sepals and five small white petals. There are two subspecies which differ mainly in the arrangement of hairs on the stem.
The top few centimeters of the stem is made up of a cylindrical inflorescence with each spikelet embedded into it and dividing it into segments which can break off.
The plant erects a tall stem which is pale green with pink or red tinting, atop which it bears a branching inflorescence with many pale to bright yellow flowers.
The inflorescence contains many leaves and a few flowers. The flowers have bell-shaped calyces of green sepals and lobed petals which may be dark red, white or purplish.
Its hairy petioles are 5-15 millimeters long with a groove on their upper side. Inflorescences are organized on short inconspicuous peduncles. Each inflorescence consists of 1-2 flowers.
The longest leaves near the base of the stem are up to long by wide. The inflorescence has widely spaced twisted green flowers with petals up to in length.
The thready leaves are no more than 5 centimeters long. The inflorescence bears widely spaced spikelets which are reddish purple in color. Each has three awns at the tip.
Leaf margin regularly toothed to finely serrate, although flower leaves may be entire. Inflorescence from the leaf axil 1-2-3 flowered. Flower stems 4-6 cm, erect bare.
The inflorescence is several centimeters long and bears many flowers with white petals just a few millimeters in length. The fruit is a silique up to 2.5 centimeters long.
Detail of flowers The leaves of this geophyte are basal. They are long, slender, lanceolate and channeled. The leaf margins are often hairy. The vertical inflorescence has many flowers.
The inflorescence is a woolly cluster of narrow, leaflike bracts laced with webby fibers. The small flowers are funnel-shaped, with yellowish throats and white to pale blue corollas.
The inflorescence bears cylindrical, oval, or nearly spherical flower heads each 2 to 5 millimeters. The head generally has no phyllaries, just a ball of tiny woolly white flowers.
The dense inflorescence is crowded with rounded, urn-shaped white flowers, each only 3 to 5 millimeters long. The fruit is a hairy, glandular drupe about 7 millimeters wide.
The stiff, sharp-pointed leaves are up to 20 centimeters in length. The inflorescence is a cylindrical panicle of tiny purple flowers. Flowering occurs in August through October.Muhlenbergia torreyana.
Actinotus suffocatus is a small, rhizomatous, mat-forming perennial herb with leaves in a basal rosette and a cup-shaped inflorescence of sessile flowers on a short, erect scape.
The inflorescence is a raceme of mustardlike flowers with yellow petals each no more than a millimeter long. The fruit is a round silique 1 or 2 millimeters wide.
Older larvae live free among spun leaves or the inflorescence. The larvae have a yellowish green body and a black head. They can be found from April to June.
The compound or decompound inflorescence will commonly have many primary branches to a length of with sub-digitate clusters that are spherical to hemispherical and have a diameter of .
The small stem bears an inflorescence of 1 to 25 flowers. The flower has 5 to 9 small white or pinkish petals often marked with darker veining or stripes.
The inflorescence is a cluster several centimeters long of white to deep blue flowers. The fruit is a lobed capsule a few millimeters long which is sticky when new.
The irregular-shaped tuber of E.zeyheri is white-ish inside. The pale, greenish-cream-coloured, fragrant, star-shaped flowers appear on a tall, thin inflorescence in December to March.
The leaves are pinnately bifoliolate, meaning that they have two leaflets attached to the sides of the petiole. The flowers grow in a panicle or corymb type of inflorescence.
The inflorescence is an open array of flowers on short pedicels. Each flower opens into five pointed lobes, each about a centimeter long and dark rose pink in color.
The inflorescence contains up to 50 dark veined pink- tinted white flowers. Anthers and pollen are yellow.Hickman, J. C. 1993. The Jepson Manual: Higher Plants of California 1–1400.
An open inflorescence usually contains functionally male and female flowers at any one time. Inflorescences range from 6–15 cm in diameter with a basal ring of coloured bracts.
The inflorescence consists of bunches of a few flowers which are either sessile or are borne on short stalks. The flower buds are ovoid and covered in a short tomentose pubescence. The individual flowers are greenish- yellow in colour, hermaphroditic with five petals in radial symmetry and are in diameter. The pedicel of the inflorescence is greyish in colour, downy and usually less than in length, although has been recorded in Zambia and Zimbabwe.
USDA Forest Service Botany in the News This plant is a perennial herb producing a basal rosette of fleshy, hairy, lance-shaped leaves up to 4 centimeters long. The inflorescence arises on a peduncle up to 25 centimeters tall with widely spaced flowers, each at the tip of a pedicel. The inflorescence also contains reproductive bulblets. Each flower has five spade- shaped petals which are white with two golden spots near the base.
Acis ionica is a bulbous plant with narrow leaves, 12–22 cm long but only 2–3 mm wide. The leaves appear after flowering, which is in the autumn. The flowering stalk (scape) is usually 8–20 cm tall, with an inflorescence composed of two to four flowers, occasionally only one or as many as six. The inflorescence is subtended by two spathes, usually extending to below the level of the highest flower.
Aloe nyeriensis is a succulent aloe plant species, endemic to Kenya. Inflorescence It grows from 1–3 metres tall, and sends up an inflorescence on a flowering stalk from 0.5-0.8 metres tall, densely packed with red flowers. A. nyeriensis grows on rocky soils of the savannah, often in communities with Acacia trees, at altitudes between 1760 and 2100 metres. It is closely related to - and often confused with - its relative Aloe kedongensis.
Hakea sericea is a large spreading, bushy shrub and may grow to and does not form a lignotuber. The branchlets are densely covered in grey-whitish short, soft, woolly hairs. The inflorescence appear in umbels of 1-6 flowers in leaf axils, pinkish in bud and maturing to white. The inflorescence rachis is long and thickly covered in woolly, short, matted white hairs toward the end and rusty coloured at the base.
Developing pitchers have laterally appressed walls and a pronounced bulge at the rear, which holds the spur upright. The spur has a closed bifurcation at this point. Nepenthes eymae has a racemose inflorescence. The male inflorescence measures up to 30 cm in length by 2.5 cm in width (flowers included), of which the peduncle (≤3 mm wide at its base) constitutes up to 11 cm and the rachis up to 20 cm.
Inflorescence of Guzmania musaica Guzmania musaica is a stemless, evergreen, epiphytic perennial plant that can reach a height of . Leaves are about two feet long, simple, with entire margins, spineless, light green with reddish and dark green transverse striations. In the central rosette of leaves grows a long stem topped by a beautiful inflorescence of pink-red bracts with many waxy tubular yellow flowers arranged in spikes. The plant blooms from June to August.
Inflorescence of Hydrangea radiata The inflorescence of silver hydrangea is a corymb. The showy, sterile flowers (white to near white) and are comparatively abundant (2-15 per bloom) and are borne around the periphery of the corymb; they are usually greater than 1 cm in diameter. The leaves of silverleaf hydrangea are large (8 to 15 cm long), opposite, serrated, ovate, and deciduous. The upper leaf surface has hairs along the veins.
The lower leaves are lance- shaped with a toothed or smooth edge and leaves higher on the plant are narrower, linear in shape, and less often toothed. The top of the stem is occupied by a long inflorescence which is an open raceme of many flowers. The top of the inflorescence bears the newest buds which are often purple in color. More mature flowers stud the stem at intervals below, each on a short pedicel.
Banksia because its inflorescence is a typical Banksia flower spike shape, in B. sect. Banksia because of its straight styles, and in B. ser. Banksia because of its robust inflorescence and hairy pistil that is prominently curved before anthesis. He added that its follicles resembled those of Banksia ornata, while the muricate seed body resembled those of B. speciosa and B. baxteri, though its obovate, crinkled cotyledons suggested an affinity with the series Cyrtostylis.
Leaves are ephemeral, growing in whorls of three on the lower branches and falling off after a short time. They are linear in shape and up to 3 centimeters long. The inflorescence is an umbel appearing at the tips of the long branches and sprouting from the sides at nodes. The inflorescence contains many small purple-tinted greenish flowers, each with a central array of bulbous hoods, and corollas reflexed back against the stalk.
This sedge produces triangular, hollow stems 30 to 120 centimeters tall. The leaves are hairy, especially on the lower parts, and the leaf sheath is tinted with reddish purple. The inflorescence is up to 60 centimeters long and made up of several spikes; those spikes near the tip are usually staminate, and those lower in the inflorescence are usually pistillate. The tip of each fruit has two or more long, thin teeth.
This sedge produces stems up to 60 centimeters tall, growing from a long rhizome. The stem just below the inflorescence is sheathed in the base of the bract, the characteristic that gives the plant its name. The inflorescence contains a terminal spike and usually at least one lateral spike. The plant reproduces by seed and by sprouting from the rhizome and the stolons, and from buds at the bases of the stems.
This is an erect plant often reaching over half a meter in height. Its foliage is rich green and dotted with glands and hairs. The sawtoothed leaves extend about halfway up the plant, with the upper half of the stem being occupied with a stout inflorescence which narrows to a point. The inflorescence has rows of leaflike bracts, between which emerge showy purple and white lipped, hooded flowers, each over two centimeters wide.
There is also some evidence that the giant inflorescence, which heats itself to 36°C, thus shines like an invisible infrared beacon in the dark of night on the jungle floor, unseen by humans but detectable by insects. The blooms of Philodendron adamantinum are able to stick a glob of resin on the otherwise smooth back of the beetles it attracts, modifying them so they are better equipped to carry pollen to the next inflorescence.
Both floating leaves and submerged leaves are borne on long petioles, a distinguishing characteristic. The inflorescence is a spike of many small flowers arising from the water on a peduncle.
The inflorescence is of simple terminal racemes, long. The cylindrical corolla tube is white, the upper lip pale blue, and the lower lip bright blue, flowering from October to December.
They are white and woolly on the undersides but green and mostly hairless on the upper surfaces. The inflorescence is a cluster of white flowers.Eriogonum exilifolium. Flora of North America.
The inflorescence is coiled in bud, but generally elongates in fruit. The pedicels are generally 0–1 mm, and the flower is bisexual with the sepals fused below the middle.
Inflorescence measurements for the formal description were taken by Volker Heinrich at the type locality on 22 July 2008, since herbarium material of the floral structures could not be located.
It grows from a rhizome. The young twigs are coated in curly hairs. The deciduous leaves are oval, leathery, and glandular. The inflorescence is a raceme of bell-shaped flowers.
The inflorescence at the end of each stem is a raceme of many small five-petalled white flowers surrounded by rounded or oval bracts with pointed, lobed, or notched tips.
The coriaceous leaves are sessile, arising from clasping sheathes which cover the stem. The congested paniculate inflorescence arises from the apex of the stem and bears small, fleshy yellow flowers.
The narrow, hairlike leaves are up to long and only a few millimeters wide. The inflorescence is a spike of flowers arranged in whorls and borne on a short peduncle.
Grass Manual Treatment. This perennial grass grows up to 80 centimeters tall. The inflorescence is usually compact, its spikelets containing 3 to 7 flowers each. The grass sometimes has rhizomes.
The inflorescence is a dense, headlike spike of many flowers up to 1.5 centimeters wide. Each flower corolla is up to 1.4 centimeters wide and white to purple in color.
The flowers are medium-sized or large. The terminal flowers are solitary in many species. In others the terminal inflorescence is cymose or racemose. The flowers are odourless and regular.
The few linear leaves are up to 3 centimeters long and occur along the stem. The inflorescence generally bears one pair of yellow flowers, each flower under a centimeter wide.
This is a perennial herb with small, threadlike, pointed leaves up to 6 centimeters long. The terminal inflorescence is a cluster of flowers with petals 1 to 2 centimeters long.
The inflorescence bears rosy red bracts and violet or white petals. It is a semi-cold hardy bromeliad that can tolerate temperatures down to 25°F for a few hours.
The flowers are bright fuchsia, with 3–6 flowers growing in whorls, widely spaced along the inflorescence. The flower is long and covered in hairs, with a pea-green calyx.
A biological assessment of Parque Nacional Noel Kempff Mercado, Bolivia. RAP Working Papers 10: 1–372. Inflorescence rarely racemose, usually paniculate having 6 - 13 whorls containing 6 - 9 flowers each.
The Female inflorescence is in raceme about 1.3 cm in length. These generally contain 2-4 flowers. The pistils bifurcate. The style is cylindrical and about 2–3 mm long.
The inflorescence is a raceme of small flowers with white to pink petals a few millimeters long. The fruit is a hairy, elongated capsule up to 8 centimeters in length.
The herbage is coated in white hairs. The inflorescence bears whorls of yellow flowers roughly a centimeter long which yield rough-haired legume pods 2 or 3 centimeters in length.
Lasura tree flowers during March–April. The inflorescence, mostly terminal, is, white in color. Individual florets are nearly 5 mm in diameter. At places these are somewhat hairy and white.
The inflorescence is made up of one to nine clusters of a few tiny flowers each. The flower is made up of several segments which are green with translucent margins.
The inflorescence is an open array of several clusters of up to 10 flowers each. The flower has rough-textured green segments with brown edges and bristles at the tips.
Cyperus javanicus inflorescence Cyperus javanicus planted in Hawaii Cyperus javanicus, also known as the Javanese flatsedge, is a sedge of the family Cyperaceae that is native to Indonesia and Australia.
Orcuttia pilosa is a small, densely hairy annual bunchgrass forming tufts up to about 20 centimeters tall when growing erect. The inflorescence is a crowded cluster of overlapping hairy spikelets.
As a parasite taking its nutrients from a host plant, it lacks leaves and chlorophyll. The inflorescence is a small cluster of tubular purple flowers 1 to 2 centimeters long.
The inflorescence is coiled in bud, but generally elongates in fruit. The pedicels are generally 0–1 mm, and the flower is bisexual with the sepals fused below the middle.
The stem bases are thick and sheathed by the hairless leaves. The inflorescence is dense, cylindrical, and narrow. It is a spikelike series of many small whitish or grayish spikelets.
The inflorescence is made up of spike- like clusters of numerous purple flowers that are bilaterally symmetric. Each cluster is across. Bracts are generally round long. Each calyx is usually .
This grass produces branching stems up to 1.2 meters tall from a network of rhizomes. The inflorescence is a narrow panicle of spikelets which are up to 8 millimeters long.
The lanceolate to somewhat ovate inflorescence is long. The glumes are long. The lemma is long, occasionally with a straight awn measuring between . The palea is either absent or vestigial.
Nepenthes argentii on Sibuyan Island. Carnivorous Plant Newsletter 34(2): 47–50. The inflorescence bears a very dense indumentum of adpressed, stellate hairs. The staminal column is covered in short hairs.
The inflorescence is a dense or loose cluster of light green to gold spikes. Some spikes occur lower on the stem as well. The flowers are covered in light colored scales.
Castilleja kaibabensis is a woody perennial herb with hairy stems and hairy, lance-shaped leaves. The inflorescence contains hairy bracts in shades of yellow and orange.Castilleja kaibabensis. Center for Plant Conservation.
The inflorescence bears one to four flower heads containing yellow disc florets and usually 8 ray florets measuring one half to one centimeter in length. It blooms from July to August.
Other important characters are the four- sided single-leaved pseudobulbs besides the raceme inflorescence with two to ten flowers.Campacci, Marcos A. (2003). Coletânea de Orquídeas Brasileiras II, Bifrenaria. Ed. Brasil Orquídeas.
Shorea bracteolata is a species of plant in the family Dipterocarpaceae. The species name bracteolata is derived from Latin (bracteolatus = with bracteoles) and refers to the persistent bracteoles of the inflorescence.
The inflorescence is covered in glandular hairs. It contains many lance-shaped yellow or orange bracts and flower corollas long. Blooming occurs in July and August. The plant reproduces by seed.
The bracts which subtend the inflorescence are longer than it. It flowers from October to February and fruits from October to June and the nuts are dispersed by granivory and wind.
They are lobed or toothed.Holodiscus dumosus. USDA International Institute for Tropical Forestry. The inflorescence is a feathery panicle of small, pinkish-white to cream colored flowers, each about 2 millimeters long.
The inflorescence is a linear array of developing fruits with a dense clump of open flowers at the tip. The bristly white five-lobed flowers are 3 or 4 millimeters wide.
They have hairs and bristles, some of which have bulbous bases. The inflorescence is a length of very hairy developing fruits tipped with a cluster of small five- lobed white flowers.
The inflorescence is a flat-topped cyme of many white flowers each 6 to 8 millimeters wide with five whiskery white stamens. The fruit is a drupe about a centimeter long.
The inflorescence arises on a stout purple or greenish peduncle up to about 14 centimeters tall. At the top is a rounded cluster of purple flowers sheathed in purple-veined bracts.
Pandanus tonkinensis is a plant species endemic to Vietnam. Pandanus tonkinensis is one of the smaller members of the genus. It has leaves up to 90 cm long. Inflorescence is terminal.
Parinari argenteo-sericea is a tree of Borneo in the family Chrysobalanaceae. The specific epithet ' is from the Latin meaning "silvery silky", referring to the pubescence of the inflorescence and flowers.
Bulbophyllum praetervisum is a species of orchid in the genus Bulbophyllum. It grows a single flower on each inflorescence, these flowers are glossy, thick, and fleshy. They exude a spicy fragrance.
They are not sticky. The inflorescences are fan-shaped to oblong. They are loose, erect, and 3–8 cm by about 2 cm. The involucral bract is shorter than the inflorescence.
The inflorescence is a series of tiny five-lobed white flowers each about 2 millimeters wide. They are surrounded by sepals which are coated in long white hairs with hooked tips.
Pinkish-green flowers grow on stalks reaching up to tall, growing in whorls spaced about apart on the inflorescence. Plants spread into large mats, with many flower stalks blooming at once.
The inflorescence is a woolly cluster of narrow, leaflike bracts laced with webby fibers. The small flowers have yellow throats and blue corollas with lobes up to half a centimeter long.
The inflorescence bears flowers accompanied by hairy, lobed red-green bracts. The flower is up to 2 centimeters long, made up of a dark-veined pink pouch enveloped in darker sepals.
The inflorescence is made up of one or two whitish to yellowish pealike flowers located in leaf axils. The fruit is a hairy legume pod up to about 1.5 cm long.
The inflorescence is a raceme of glandular flowers, each with four notched white to pink petals a few millimeters long. The fruit is an elongated capsule up to 6 centimeters long.
The inflorescence is short cyme of funnel-shaped flowers each just under a centimeter long. The flower has a yellow-throated white corolla set in a calyx of narrow, pointed sepals.
The plants have culms that grow high, and deep-green to yellowish-green leaves measuring 2–5 mm wide. The inflorescence is typically a single terminal spike lacking a spike bract.
The inflorescence is a panicle-like cluster of white flowers up to about 7 centimeters long. The fruit is a rough, lobed capsule about half a centimeter long containing three seeds.
The inflorescence is about 10 cm long.Parnell, J. and Curtis, T. 2012. Webb's An Irish Flora. Cork University Press The fruit is a nutlet with a transparent coat containing the seed.
Inflorescence is a panicle or raceme of up to 20 flowers. Berries are dark red, narrowly egg-shaped, up to 15 mm long.Schneider, Camillo Karl. 1905. Bulletin de l'Herbier Boissier, sér.
Studies suggest that there has been selection for increased pollen delivery, achieved through greater inflorescence size, and it seems probable that male-male competition is commonly part of that selection pressure.
The inflorescence is a raceme of many yellow flowers with six pointed tepals no more than a centimeter long. The fruit is a lance-shaped capsule containing many bristle-tailed seeds.
US Forest Service Fire Ecology The leaves are up to 26 centimeters long and rough-haired along the margins. The inflorescence is an open panicle of spreading branches bearing grayish spikelets.
The inflorescence is a cluster a few centimeters wide, with each bearing three white petals surrounded by a few thin sepals. The fruit is a capsule less than a centimeter wide.
The leaf margins have irregular and very shallowly rounded teeth, and are yellow-green or dark green above, and light green below. The margins are very minutely fringed, and there are appressed hairs on the midrib beneath. The inflorescence is a spike and is terminal on the side branches. It has a covering of long soft weak hairs which are clearly separated but not sparse and is 2–4 cm long. The inflorescence stalk is 1–2 cm long.
The flowers are white with a pink tinge that gradually fades, five petaled, with an inflorescence consisting of a cyme with 4–6 flowers. The central flower of the inflorescence is called the "king bloom"; it opens first and can develop a larger fruit. The fruit matures in late summer or autumn, and cultivars exist in a wide range of sizes. Commercial growers aim to produce an apple that is in diameter, due to market preference.
The inflorescence is axillary, with and a two- flowered umbel or a four-flowered raceme or spike; there are nearly orbicular bracts beneath each flower. The flower has six free petals. The stamens are nearly equal, and the anthers are dorsifixed and versatile, having a short sterile tip with the free part of the filament about 2 mm long. The peduncle is 6–9 mm long and up to 20 mm when the inflorescence is a raceme.
M. bidwillii is an erect to spreading plant, the branches and leaves of which are smooth (or having a few scattered hairs on the inflorescence axes). The leaves are linear to oblanceolate and rounded at the tip. The leaf blade is from 1.5 to 3 cm long and 1.5 to 3 mm wide, with obscure venation and an obscure petiole. The inflorescence a 2-flowered simple umbel on a peduncle which is from 3 to 6 mm long.
Flora de la Península de Yucatán Tillandsia variabilis is an epiphyte growing in the branches of various trees in moist forests. It is up to 40 cm long including the inflorescence, usually single but occasionally in clumps. Leaves are narrowly triangular, soft and brittle, up to 30 cm long. Inflorescence is usually simple, sometimes with 2-3 branches but never palmately branched. Bracts are red, green or purple, less than 1 cm wide, covering and obscuring the rachis.
They appear in clusters, each flower up-turned, on a tiny inflorescence that sprouts from the tip of the stem. Each stem usually only produces a maximum of one inflorescence. The flowers of different species are in a range of colours; most emit unpleasant odours, especially the darker red or brown coloured ones. The compact, mat-forming stems are very similar to those of the related genus Duvalia, and the two are often confused when not in flower.
The much branched monoecious inflorescence forms below the leaf bases, ringing the trunk with cream-coloured male and female flowers. Both sexes carry three sepals and three petals and in both cases the sepals are two or three times longer than the petals. The inflorescence becomes pendent as the large fruit set; the beaked, ovoid fruit are red to purple to green; each fruit contains one seed.Riffle, Robert L. and Craft, Paul (2003) An Encyclopedia of Cultivated Palms.
Historical model of the inner part of the inflorescence, the spadix with the flowers and ring of small hairs. Botanical Museum Greifswald. The flowers are borne on a poker-shaped inflorescence called a spadix, which is partially enclosed in a spathe or leaf-like hood of varying colour. The flowers are hidden from sight, clustered at the base of the spadix with a ring of female flowers at the bottom and a ring of male flowers above them.
These pinnae are arranged on a single plane on each side of the rachis, such that the pairs form a V-shape down the leaf blade. The pinnae are sized in length and in width in the middle of the leaf. The developing inflorescence is protected within a hairless, woody spathe in length, with the enlarged part of the spathe being long and in width. The inflorescence is branched with 7-35 rachillae (branches) which are in length.
Petioles range from to over in length, while the rachis (which bears the leaflets) can be to over long. Inflorescences are borne singly emerging from the leaf axil. Flowers grow in triplets along the inflorescence; each female flower is flanked by two male flowers; elsewhere along the inflorescence male flowers grow singly or in pairs. Ripe fruit can be yellow, orange, red or purple-black (other colours are present in a few species) and range from long.
The laminar glands are pale, pointed, and densely placed; while the intramarginal glands are black, small, and few in number. The inflorescence is 50-flowered from 1–3 nodes, but can also flower from 1-3 lower nodes; the shape of the whole inflorescence is pyramidal to cylindric. The flowers are 12–18 mm in diameter; their buds are ellipsoid and acute. The sepals are equal and acute and measure 4–6 by 1–3 mm.
Carex archeri grows up to high, with leaves less than wide. Its inflorescence comprises a single spike subtended by a bract that is longer than the inflorescence. The spike contains few flowers, with the female flowers towards the base of the spike, and a very short portion towards the tip containing male flowers. The glumes of the female flowers are long, and the utricles that form in the female flowers are long, with a notched beak.
Brodiaea coronaria is a perennial herb growing from a corm and producing an erect inflorescence with a few basal leaves. The inflorescence is up to about 25 centimeters tall and bears lilylike flowers on an array of pedicels. Each flower is a tube several centimeters long opening into a bell-shaped corolla of six bright purple lobes each up to 3 centimeters long. In the center are three stamens and whitish sterile stamens known as staminodes.
Inflorescence The yellow- green inflorescence is a panicle that reaches a length of about 4.5 to 7 centimetres. The panicle branches are hairy and each carry an elongated, flattened spikelet that grows to about 9 to 11 millimetres in length. The glumae are unkempt and shorter than the spikelets, the lower one is single- veined, the upper one is three-veined and 4.9 to 5.8 millimetres long. The five-veined lemmas reach a length of 6 to 7.3 millimetres.
Nepenthes attenboroughii has a racemose inflorescence up to 80 cm long. The male flower spike bears approximately 100 pedicellate flowers on a rachis up to 45 cm long and is recorded to bifurcate on occasion. The flowers lack bracts and produce red tepals that are broadly ovate with an obtuse apex. The female inflorescence is shorter, to 65 cm long, never bifurcates, and bears up to 70 densely arranged flowers on a compact rachis up to 20 cm long.
Telopea speciosissima floral morphology In many genera of Proteaceae the inflorescence is very large and showy, often in bright colours, consisting of many small flowers densely packed into a compact head or spike. The individual flowers within the inflorescence also give Proteaceae species a unique look. Telopea species are long-lived, perennial plants that re-sprout from lignotubers after fire. After a few years of fire, re-sprouting stems produce the terminal flowers which continue the flowering cycle annually.
The inflorescence is an umbel of 18 to 23 bell-shaped pink flowers each about a centimeter long. Blooming occurs in June through September. The plant has a strong onion scent.Allium gooddingii.
It has nitrogen-fixing root nodules. The plant grows tall. The hairless leaves are compound, divided into a number of leaflets. The inflorescence is a raceme of white, pink, or purple flowers.
The inflorescence is an erect stalk bearing one white to pale lavender flower just a few millimeters wide. The fruit is a capsule up to 5 millimeters wide containing many tiny seeds.
The leaves are flat. The inflorescence is single group of 3-5 green and red flowers. The central flower has no bracts, unlike the surrounding flowers. It flowers from April to October.
Carex straminiformis produces dense clumps of stems 20 to 50 centimeters tall with leaves up to about 25 centimeters long. The inflorescence is a dense spherical brown cluster of distinct flower spikes.
Melica torreyana is a perennial bunchgrass with dense clumps of stems up to a meter-3 feet long. The inflorescence is a narrow panicle of small spikelets each under a centimeter long.
Setaria parviflora. USDA NRCS Plant Fact Sheet. The inflorescence is a compact, spikelike panicle up to 8 or 10 centimeters long. Surrounding each spikelet are up to 12 yellow or purple bristles.
The inflorescence contains up to 40 spikes each up to 3 inches long.Spartina cynosuroides. USDA NRCS Plant Fact Sheet. This grass grows in flooded saline soils such as those in salt marshes.
As with other members of E. subsect. Spathacea Rchb.f. 1861, the racemose inflorescence bears enlarged spathaceous floral bracts. The green, non-resupinate, fleshy flowers are partially covered by the large, dolabriform bracts.
It has tiny leaves 3 or 4 millimeters long and a red or purplish inflorescence containing one flower no more than 4 millimeters long.Geocarpon minimum. Flora of North America.Mackenzie, Kenneth Kent 1914.
Grass Manual Treatment. This rhizomatous perennial grass has thick stems which can exceed in height. The leaf blades are up to long. The inflorescence is a panicle with up to 7 branches.
The stem grows to a maximum height near . The inflorescence is a cluster of three to five blue or blue-green flowers up to long. The fruit is a tubular capsule.Gentiana glauca.
It is a strongly branching woody shrub, average height , maximum height . The leaves are leathery and lance-shaped. Its flowers are white to rosy white and sit in a medium-sized inflorescence.
If the inflorescence is located on an erect stem it bends the stem over with its weight. The flowers self-pollinate. The fruit is a cylindrical capsule 1 to 2 centimeters long.
The inflorescence is a series of tiny flowers with white five-lobed corollas no more than 3 millimeters wide. The fruit is a minute nutlet with a surface covered in long prickles.
The flower heads of the small cryptic pagoda M. palustris contain three to six individual flowers, and the leaves in the inflorescence are tightly overlapping, not patent as in both larger species.
Flowers are pink, about 2.5cm in diameter, and form a compact terminal inflorescence, with smaller axillary inflorescences. Edees, E.S., Newton, A. and Kent, D.H., 1988. Brambles of the British Isles. Ray Society.
The inflorescence is composed of two or three flowers emerging from the leaf axils. Each flower has pointed sepals tipped with awns. The flower has a purplish tube and a pinkish corolla.
The leaves are no more than 3 to 5 centimeters long and just a few millimeters wide. The inflorescence is a small, narrow, partially sheathed series of short branches bearing small spikelets.
The linear or lance-shaped leaves are up to 3 centimeters long. The hairy, glandular inflorescence is a cyme of five-lobed lavender flowers each no more than half a centimeter long.
Furthermore, each phyllode extends into a spine. Tolerate frosts to . A. alata blooms between April and December. The inflorescence is simple with mostly two flowers per axil, but sometimes distributed in racemes.
The glandular inflorescence bears wide-mouthed tubular flowers up to 2.2 centimeters long in shades of blue-purple. The flowers are mostly hairless except for thin glandular hairs on the outer surfaces.
The inflorescence is branched to a single order, with 15-35 rachillae (branches) 7-20cm long. It is monoecious. The flowers are generally purplish. The staminate (male) flowers are 8-10mm long.
Oxytropis podocarpa. Fabaceae of the Canadian Arctic Archipelago: Descriptions, Illustrations, Identification, and Information Retrieval. Version: 15 November 2000. The inflorescence is a raceme of one or two purple or blue-violet flowers.
This is a tufted perennial bunchgrass growing up to a meter tall. The inflorescence is open with spreading branches. The spikelet has a twisted awn up to 2.5 centimeters in length.Achnatherum richardsonii.
17 . It has panicles of cream-colored pointed flowers produced in spring. The loose, hemispherical inflorescence has a length of 6 to 16 centimeters and a width of 6 to 16 centimeters.
Dioscoreophyllum gossweileri is a plant species native to Angola. It is a twining vine with deeply tri-lobed leaves and a racemose inflorescence. Dioscoreophyllum gossweileri Exell, J. Bot. 73(Suppl.): 10. 1935.
Trifolium cyathiferum is a low growing annual plant. Jepson The inflorescence is many flowered and bowl shaped. Flowers are white to yellow with pink tips. The bloom period is May to August.
Thus, the pseudanthium represents an evolutionary convergence of the inflorescence to a reduced reproductive unit that may function in pollination like a single flower, at least in plants that are animal pollinated.
It is a perennial growing tall. 2 to 7 lanceolate to narrow elliptic leaves should be present. The inflorescence is a terminal racemic structure, long with 15 to 60 whitish-green flowers.
The inflorescence is topped by a head (coma) of up to 30 bracts, sometimes quite small. The plant lacks the purple coloration found other large species of Eucomis, such as Eucomis comosa.
Phleum alpinum is a perennial bunchgrass forming loose clumps 20 to 60 centimeters tall. The inflorescence is a cylindrical to oval mass of spikelets up to 6 centimeters long and 1.2 wide.
The inflorescence is a solitary tubular flower around a centimeter long. It has a flat white or pale pink or blue corolla with five lobes each just under a centimeter in length.
The inflorescence is a solitary flower at the tip of each stem. The flower is white or light pink or lavender with five rounded lobes. It is just over a centimeter long.
Its leaves are basal and grass-like. Its inflorescence is a long, compact spike. It typically flowers in late spring and early summer, although later season flowering can be induced by rainfall.
Inflorescence of Crossyne guttata Flowers of Crossyne guttata Lorate immature leaves of Crossyne guttata Crossyne is a genus of African plants in the Amaryllis family.Salisbury, Richard Anthony. 1866. Genera of Plants 116.
It is similar to Protea effusa, primarily differing in having conically-shaped receptacles within the inflorescence, and also to P. pendula, from which it differs by having wider leaves with indistinct venation.
The inflorescence is a hanging cluster of spherical to urn-shaped manzanita flowers each about half a centimeter long. The fruit is a hairless drupe between one half and one centimeter wide.
In the wild, all Fascicularias are terrestrial, saxicolous (growing on rocks) or epiphytes. It is cultivated in gardens for the dramatic bright crimson colour of its leaves contrasting with the blue inflorescence.
The inflorescence is a coiled cyme of flowers that uncoils as the fruits develop. The flowers have corollas less than half a centimeter wide and hairy, bristly sepals.Cryptantha incana. Jepson Manual Treatment.
The inflorescence is a raceme of several tiny white flowers each under a centimeter wide. The fruit is a silique measuring 4 to 8 centimeters in length and containing many small seeds.
Versieux, L.M., Wendt, T., Batista Louzada, R. & das Graças Lapa Wanderley, M. (2008 publ. 2009). Bromeliaceae da Cadeia do Espinhaço. Megadiversidade 4: 98-110. Hohenbergia stellata exhibits sharp spines in its inflorescence.
The inflorescence is a cluster of pointed yellow-green, pink, or pale purple, hairy bracts. Between the bracts appear the small purple-spotted yellow flowers, which are pouched with tiny, protruding stigmas.
The inflorescence is a tight cluster of white flowers with 3 to 5 petals each a few millimeters long. The fruit is a capsule containing up to 15 minute shiny black seeds.
The hairy, glandular inflorescence is a one-sided curving or coiling cyme of funnel- or bell-shaped flowers. Each flower is about half a centimeter long and white to cream in color.
The rachis is 30–74cm in length. The 15-29 pinnae (leaflets) on each side of the leaf rachis are linear with an acuminate apex and inserted at a regular distance on the same plane per side of the leaf, so that each pair of pinnae forms a neat 'V'-shape. These pinnae are 13-40cm long and 0.3-0.8cm wide in the middle of the rachis. Similarly to B. eriospatha, it has woody spathes (in which the young inflorescence is developing) with the outside surface densely covered in a furry layer of lanate (woolly) tomentose indumentum; these differ from the spathes of that species by the hairs being shorter and darker purplish-brown. The spathe is 33–40cm in length, with an enlarged part 10-18cm long and 3.5-4.5cm wide. The inflorescence is branched and up to 17cm long. The inflorescence has a 27-32cm peduncle and a lanceolate prophyll 7-14.5cm long. The rachis of the inflorescence is 1-7.5cm long and has 3-18 rachillae (branches) which are 6-12cm long.
The leaves are green in color and waxy in texture. The inflorescence is an erect, wide open array of many flowers. The flowers have yellow petals with red-tinged or white-speckled undersides.
Prepared for the USDA Forest Service, Rocky Mountain Region, Species Conservation Project. September 24, 2004. The short inflorescence has yellow flowers. This plant grows in cracks and crevices on rock outcrops and cliffs.
The pitcher lid or operculum is reniform to cordate and has no appendages. An unbranched spur (≤15 mm long) is inserted at the base of the lid. Nepenthes bicalcarata has a paniculate inflorescence.
The shrub stands tall, with leaves long. The leaves close in the dark. The inflorescence looks like a yellow candle. The fruit, shaped like a straight pod, is up to 25 cm long.
The inflorescence is a panicle with minute reddish-brown flowers. The fruits are rounded, sticky and yellow when ripe, the carpels developing long, horn-like processes. The fruits are about long and wide.
Muhlenbergia reverchonii. NatureServe. This perennial bunchgrass produces erect stems up to 80 centimeters tall. The hairlike leaves are up to 35 centimeters long. The inflorescence is a panicle of brown to purplish spikelets.
It produces clumps of stems up to a meter tall. The inflorescence is a dense, tangled cluster of many flower spikes up to about long. Tolerates fluctuating water levels and periods of drying.
Melica californica is a perennial bunch grass, generally with rhizomes, producing a dense cluster of stems up to about in maximum height. The inflorescence is a narrow series of purple-banded green spikelets.
Silene caliacrae is a biennial to perennial herb, tall when mature. The leaves are opposite and entire. The inflorescence is long, comprising a number of bisexual flowers, each with a white corolla wide.
Gobierno de Canarias, p. 150 It is a low woody shrub, average height , maximum height . The leaves are leathery, spiny and lance-shaped. Its flowers are white and sit in a compact inflorescence.
American Journal of Botany 92(1), 167-78. They grow from thick rhizomes. The leaves are lance-shaped to oblong. The inflorescence takes the form of a spike, a panicle, or a raceme.
Stems are square in cross-section, up to 40 cm long. Leaves are in whorls of 6-8 narrowly oblanceolate leaves, thick and somewhat succulent. Inflorescence is an elongated panicle of yellow flowers.
The stem reaches a meter in height with an inflorescence of 7 to 10 centimeters. The spikelets grow on short, wavy stalks and each has three florets with long, protruding stamens during flowering.
The forewings are uniformly pale to medium brown. The hindwings are usually lighter and sparsely scaled.TOLweb The larvae feed on Yucca whipplei. They feed primarily in the basal portion of the inflorescence stalk.
The inflorescence arises on a slender, hairy peduncle up to 40 centimeters tall. Thin branches bear flowers and reproductive bulbils. Each flower has spade-shaped white petals, the upper ones dotted with gold.
They are up to 6.5 centimeters long. The inflorescence is a cluster of up to 20 flowers, or sometimes more. The petals are white or rose-pink. The fruit is a hairy nutlet.
The inflorescence is a spreading or flat-topped array of many small, star-shaped flowers with red or pink petals up to a centimeter long each, and stamens with red or purplish anthers.
Inflorescence is up to 45 mm long. Flowers are white, some hermaphroditic (male and female together) but others pistillate (female only). Achenes are brown, triangular in cross-section, up to 4 mm long.
Its species are perennial aquatic plants (or hydrophytes) with prostrate and densely branched stems. The inflorescence is can have one to 30 conspicuously attractive flowers, mostly lavender to pink in colour, rarely white.
Journal of Evolutionary Biology 25(1): 90–102. The lid is very long, narrow, and cuneiform. It is never reflexed beyond 90 degrees relative to the mouth. Nepenthes inermis has a racemose inflorescence.
The inflorescence is a raceme of several blue or purple pealike flowers each about long. The fruit is a hairy oval beak-tipped legume pod up to long containing smooth kidney-shaped seeds.
The inflorescence bears widely spaced narrowly cylindrical spikelets which hang sideways off the stem, resembling semaphore signals. Each spikelet may be up to 4.5 centimeters long and may contain up to 16 flowers.
The inflorescence is a rounded cluster of flowers held on a peduncle which may be erect and several centimeters tall or nearly nonexistent. The purple flowers are sheathed in dark-veined white bracts.
Arisaema thunbergii subsp. urashima is a herbaceous perennial plant. It is widespread through the woodlands of Japan, especially near the coast. The plant has a very curious inflorescence, and is popular in horticulture.
It grows as an erect annual herb up to in height, though normally not more than high. It is sparsely hairy, with few branches except for the branched inflorescence. The flowers are yellow.
The leaves are divided into several narrow, threadlike linear lobes. The inflorescence is a woolly cluster of narrow, leaflike bracts laced with webby fibers. The small flowers have white to light blue corollas.
The inflorescence is a cluster of 3 to 8 flowers each up to about a centimeter long. The petals are yellow, often with dark lobes. The fruit is a curved, beaked legume pod.
Achillea pratensis has pinnate leaves with a low number of leaflets compared to other A. millefolium and related species (15 per side on average). The inflorescence is comparatively loose. The plant is tetraploid.
It flowers in late spring to early summer around November and produces an inflorescence containing 6 to 10 white flowers. This species does not produce fruit and only reproduces asexually by root suckering.
The inflorescence include separate male and female flowers. The flowers are pungent, creamy- yellow and have no petals. The fruit is a capsule that contains three large seeds; it opens explosively when ripe.
Flowers are produced on a reduced inflorescence in Alluaudia comosa; only the end flower develops, and is set on a very short axis. Flowers are dioecious (male and female flowers on separate plants).
The inflorescence is a raceme about 50 cm long. The bracts are leafy. The stalk of the inflorescense is 2–6 cm long. The sepals are up to 2 mm long and free.
Nestegis species are evergreen trees or shrubs. The leaves are opposite, simple, entire, and coriaceous. The inflorescence is axillary, decussate, sometimes terminal and somewhat paniculate. The flowers are either bisexual or functionally unisexual.
The inflorescence is a panicle of white or pink conical or urn-shaped flowers each 6 to 8 centimeters long. The fruit is a spherical reddish-brown drupe 1 to 1.5 centimeters wide.
Foleyola billotii was first described by René Charles Maire. The individual flowers have purple petals and are spaced along the inflorescence. Its growth habit is as a shrub. It grows in arid areas.
Leucopogon foliosus is a plant in the family Ericaceae native to Western Australia. It was first described in 2016 by Michael Hislop. The species epithet, foliosus ("leafy", "many-leaved") describes the leafy inflorescence.
Deschampsia danthonioides has stems growing solitary or in loose clumps up to 40 to 60 centimeters tall. The inflorescence is a narrow to open array of thin branches bearing small V-shaped spikelets.
Most frass is ejected out of the mine. Older larvae live free among spun shoot tips in the spun inflorescence and feed on the flowers. Larvae can be found from May to June.
The inflorescence is paniculate and simple or branched with a few side risps. The perigon is blue or purple. The helmet is usually wider than high. The tepals are bare on the outside.
Related to Zygopetalum. Stems short, leafy, usually forming pseudobulbs, 1- to 3-leaved. Leaves petiolate, linear to oblong, narrow, pleated, lightly veined. Inflorescence lateral, erect, slender, branched or unbranched, numerous to few-flowered.
They vary in shape. They are glandular in most species. The inflorescence is a solitary flower head. The head can have 15 or more ray florets, while some taxa lack any ray florets.
Red blotches are present on the waxy inner surface. The peristome may be yellow or red striped, while the lid is green to yellow and commonly red on its lower surface. Nepenthes kerrii has a racemose inflorescence up to 130 cm long. In male plants, the inflorescence reaches 90 cm in length, of which the peduncle can constitute up to 65 cm and the rachis up to 27 cm, and bears around 120 flowers singly on pedicels measuring 6–8 mm in length.
Part of an inflorescence and single blossom This is a perennial herb growing from a caudex in the water or mud. It produces lance-shaped leaves 12 to 20 centimeters long and 4 wide on long petioles; leaves which remain submerged in water are smaller and less prominently veined. The inflorescence is mostly erect and up to half a meter tall. It is a wide array of small pink-petalled flowers, which open in the morning, from June until August.
A flowering plant of N. rajah Nepenthes rajah seems to flower at any time of the year. Flowers are produced in large numbers on inflorescences that arise from the apex of the main stem. N. rajah produces a very large inflorescence that can be 80 cm, and sometimes even 120 cm tall. The individual flowers of N. rajah are produced on partial peduncles (twin stalks) and so the inflorescence is called a raceme (as opposed to a panicle for multi-flowered bunches).
Mutations in LFY, AP1, and similar promoting genes can cause conversion of flowers into shoots. In contrast to LEAFY, genes like terminal flower (TFL) support the activity of an inhibitor that prevents flowers from growing on the inflorescence apex (flower primordium initiation), maintaining inflorescence meristem identity. Both types of genes help shape flower development in accordance with the ABC model of flower development. Studies have been recently conducted or are ongoing for homologs of these genes in other flower species.
Little has been published on the ecology of B. oligantha. Its lifespan is probably around 10 to 30 years. Six species of honeyeater have been observed feeding at its flowers, as have insects including honeybees, ants, butterflies, beetles and native bees. Both birds and insects function as pollinators, but honeybees are probably not very effective: in one study only about 4% of honeybees collected pollen, and they tended to move from inflorescence to inflorescence on the same plant, rather than moving between plants.
Amorphophallus titanum, the titan arum, is a flowering plant with the largest unbranched inflorescence in the world. The talipot palm, Corypha umbraculifera, has a larger inflorescence, but it is branched rather than unbranched. A. titanum is endemic to Sumatra. Due to its odor, like that of a rotting corpse, the titan arum is characterized as a carrion flower, and is also known as the corpse flower or corpse plant (—bunga means flower, while bangkai can be translated as corpse, cadaver, or carrion).
These are perennial herbs growing from fleshy root systems that range from slender to tuberous, and are occasionally stoloniferous. Most of the leaves are basal, but some species have leaves higher on the stem before the inflorescence matures, often taking the form of a sheath around the stem. The inflorescence is a terminal spike with flowers arranged in a characteristic loose or dense spiral. As in most other orchids, the flowers are resupinate, twisting during development into an upside-down position.
Mimetes palustris or cryptic pagoda is an evergreen shrub, assigned to the family Proteaceae. It has horizontal sprawling shoots as well as upright, unbranched shoots usually about ½ m (1½ in) high. The leaves are entire and stand out on the lower parts of the shoots, but are overlapping and pressed tidly against each other near the inflorescence, almost like a snakeskin. The inflorescence consists of several flowerheads, each containing three clear yellow flowers that are longer than the subtending leaves.
Muellerina celastroides is an erect or spreading plant which is smooth except for the inflorescence axis which is covered with minute, brown, densely matted woolly hairs. The leaves are oblong to elliptic and 2.5-7 cm long and 15-25 mm wide, with a rounded apex and an attenuate base. The inflorescence is a raceme of 1–3 pairs of triads, with the stems of lateral flowers being 3–6 mm long. The calyx is entire and about 1 mm long.
Allium amplectens is a species of wild onion known by the common name narrowleaf onion. It is native to British Columbia, Oregon, Washington State and California, where it grows in woods and especially in clay and serpentine soils.Kew World Checklist of Selected Plant FamiliesFlora of North America v 26 p 262 Allium amplectens grows from a pinkish-brown bulb and sends up a naked green stem topped with an inflorescence. When closed, the inflorescence is wrapped in bright pink to magenta bracts.
Botanical illustration of Synosma suaveolens (1913) Hasteola suaveolens is a perennial herb sometimes as much as 240 cm (8 feet) tall, hairless throughout, unbranched below the inflorescence. The spearhead shaped leaves are long and wide with serrated (toothed) edges. The plant flowers in late summer or early fall. The inflorescence is one or several roughly flat topped clusters of several to many flower heads consisting entirely of 18–55 white or very pale yellow disc florets, but no ray florets.
The main distinguishing characters of S. graminifolius are its papery (chartaceous) spikelet glumes that have reddish- purplish streaking throughout. Another key character of S. graminifolius is that its lower primary inflorescence bracts are widened at the base. Schoenus auritus also has lower primary inflorescence bracts that are widened at the base; however, that species has firmer glumes. The basal leaves of S. graminifolius are usually relatively long and grass-like, so that they are almost as long or longer than the flowering stems.
Pimelea physodes is a shrub that typically grows to a height of and has a single stem at ground level. The leaves are arranged in opposite pairs, more or less sessile, egg- shaped to narrow elliptical, long and wide and the same shade of green on both sides. The flowers are arranged in a bell-like inflorescence similar to those of some species of the distantly related darwinias, especially Darwinia macrostegia, (Mondurup bell). The peduncle of the inflorescence is long.
The describing authors of N. gantungensis identified N. deaniana and N. mira as its closest relatives. All three species are only known from isolated Palawan peaks. Nepenthes gantungensis can be distinguished from both on the basis of its typically shorter and narrower laminae, which have a more acute apex and base, as well as on the structure of the inflorescence, in which all flowers may be borne singly on pedicels. Compared to N. deaniana, the inflorescence of N. gantungensis is usually considerably longer.
Nepenthes hamata has a racemose inflorescence. The male inflorescence is 8–15 cm long, of which the peduncle constitutes 2.4–10 cm and the rachis up to 8 cm. The peduncle has a basal diameter of around 3 mm. Flowers are borne solitarily on ebracteate pedicels measuring 10–15 mm in length by 0.1–0.3 mm in width. The pedicels number around 22 per inflorescence. Tepals are elliptic, reflexed, and 1.5–3 mm long by 1–1.5 mm wide. Androphores are 1–2.5 mm long and bear anther heads measuring 0.6–0.8 mm by 0.8–1.4 mm. One infructescence was measured at 8.5 cm long by roughly 5 cm wide (fruits included), with a peduncle measuring 6.5 cm in length and having a basal diameter of 2.25 mm.
The inflorescence is a cluster of 3 to 7 funnel-shaped flowers. The lobes of the corolla are up to a centimeter long and white with 2 magenta marks at the base of each.
Satyrium erectum (Pienktrewwa) habit and habitat. Note flattened outer leaves. Satyrium erectum detail of inflorescence Satyrium erectum, habit in bud Satyrium erectum is a species of orchid endemic to southwestern and western Cape Province.
It may spread to form a colony. The oppositely arranged leaves are lance-shaped and mint-scented. The inflorescence contains tubular reddish purple flowers with purplish bracts beneath. The flowers are attractive to insects.
The branching inflorescence holds up to 25 widely spaced flowers, which are usually bright deep blue, and occasionally lighter blue or white, depending on subspecies. The spur is between one and two centimeters long.
Inflorescence axillary, solitary. Flowers numerous, arranged on a simple or lobed androgynous receptacle. Receptacle axillary, solitary, discoid, 5-angled, to 1.5 cm across, marginal lobes to 0.5 cm long; peduncles to 2 cm long.
The inflorescence is a solitary flower head with a small, hard, cuplike involucre of about 8 fused phyllaries. From the involucre bloom about 8 golden ray florets around a center of hairless disc florets.
The branching inflorescence bears many flowers, each with small bracts at its base. The flower has five oval-shaped petallike lobes each a few millimeters long. Until 2004 it was placed in genus Centaurium.
The inflorescence produces several small flowers with four oval petals just a few millimeters long and lavender in color with yellow-tinted bases. The fruit is a club-shaped capsule roughly a centimeter long.
Single flower of a Gasteria Gasteria brachyphylla Gasterias are recognisable from their thick, hard, succulent "tongue-shaped" leaves. Their inflorescence is also unique, with their curved, stomach-shaped flowers, which hang from inclined racemes.
They may be known generally as bloodgrasses.Isachne. USDA PLANTS. These are annual and perennial grasses. The stems are hollow, the leaves are often nerved, and the inflorescence may be an open or narrow panicle.
The inflorescence is a compound umbel of yellow flowers with up to 12 unequal rays measuring up to 6 centimeters long each. The fruit is rounded, ribbed, and only 2 or 3 millimeters long.
Petioles are 4–20 mm long. The inflorescence is a thyrse with 20-80 flowers. Peduncles measure 5–12 mm in length. The flowers are greenish-yellow, with stamens opposite the spoon-shaped petals.
Propagate by adventitious plantlets which form on the inflorescence. A rather demanding species, now rarely seen. The flowers open in the later morning hours only for about 2 hours. After this, it closes completely.
It is sometimes clumpy in form. The leaves are linear in shape and about 1 to 2 centimetres in length. The inflorescence is a solitary flower with five sepals and five small white petals.
The top of the stout stem is occupied by an inflorescence in a compound umbel arrangement, with the webbed rays of the umbel up to 10 centimeters long each. The flowers are generally yellowish.
Perennial with woody stock. Leaves in a basal rosette, pinnatifid with rounded lobes; margins subspinose. Scape up to 80 cm, with a few small bracts. Inflorescence a dense corymb of up to 20 heads.
The inflorescence is a dense cluster of flowers, each flower surrounded by six white to pink hairy bracts tipped in hooked awns. The flower itself is only a few millimeters wide with jagged tepals.
The inflorescence is somewhat lance-shaped, with branches appressed, spreading upwards along the stem axis. Male and female inflorescences look similar. They may hold up to 70 spikelets each, which are purplish in color.
Inflorescence about 35 cm long, a collection of umbels in a paniculate array. Fruits spherical, about 4 mm in diameter, with 5 seeds each.Wen, Jun. 2001. Aralia frondiniana (Aralacieae), a new species from Indonesia.
Clarke, C.M. 2001. A Guide to the Pitcher Plants of Sabah. Natural History Publications (Borneo), Kota Kinabalu. The inflorescence of N. × trusmadiensis may be up to 50 cm long and has two-flowered pedicels.
The lid is similar to that of the lower pitchers. Nepenthes thorelii has a large racemose inflorescence. The peduncle is 8 to 18 cm long, while the rachis is 50 to 70 cm long.
The inflorescence produces tubular flowers with wide lipped mouths. The flower is blue-purple in color, just under long, and hairless except for hairs on the floor of the mouth and on the staminode.
The inflorescence consists of multiple fluffy, red or pinkish-white capitula in clusters. These lack the typical ray flowers of the composites. They have multiple, much-branched woody stems. The petioles are rather long.
The nodding inflorescence produces flowers with yellow petals 2 or 3 millimeters long and usually spotted with red near the bases. The fruit is a straight or coiling capsule up to 3 centimeters long.
The leaves are narrow, linear in shape, with edges rolled upward nearly into a tube. The long inflorescence bears funnel-shaped lavender, pink, or pale blue-purple flowers up to 1.5 centimeters in length.
The nodding inflorescence produces flowers with yellow petals each a few millimeters long and sometimes dotted with red near the bases. The fruit is a straight or coiling capsule up to 5 centimeters long.
The inflorescence is a dense cluster of flowers, each flower surrounded by hairy, bristly white bracts tipped with hooked awns. The flower is 4 or 5 millimeters long and white to pink in color.
The inflorescence is a dense cluster of flowers, each flower surrounded by six hairy bracts with hooked awns at the tips. The flower is white to red and only 2 or 3 millimeters wide.
The inflorescence is a narrow panicle up to 15 centimeters long by 2.5 wide. The spikelet has a sharp tip and a long, hairy awn which may exceed 5Achnatherum thurberianum. Grass Manual Treatment.Achnatherum thurberianum.
Leaves are attached to petioles that are long. The inflorescence is cymose and all parts are glabrous to puberulous with a length of . The pedicels are long. The calyx lobes triangular with ciliate margins.
Most of the plant is silky-hairy in texture. The inflorescence holds one to three pinkish-yellow flowers roughly 1 cm long. The fruit is a dehiscent legume pod up to 2.5 cm long.
The laminar adaxial surface is covered in insect-trapping glands. Each rosette produces 1–4 raceme inflorescences, which are long. Each inflorescence bears 30–50 white flowers, with flowering occurring from March to June.
The hairy inflorescence is a one-sided curving or coiling cyme of bell-shaped flowers. Each flower is roughly half a centimeter long and white to purple in color with a pale yellow throat.
B. victoriae's inflorescence is orange, long. After flowering, up to 30 follicles develop in the flower spike. These are usually concealed by withered flower parts, which persist on the spike for a long time.
The herbage is coated in silvery silky hairs. The inflorescence is a small bundle of flower whorls, each flower about a centimeter long and purple in color with a yellowish patch on its banner.
The inflorescence bears greenish or purplish flowers. There are two subspecies of this plant, both very rare. One individual of ssp. lobata was found in Maui in 1982 after several decades of no observations.
The inflorescence is an open array of flower heads with a fringe of violet ray florets around a center of yellow disc florets. The fruit is a hairy achene with a long white pappus.
The flowers have umbellule inflorescence with 10-20 white flowers. These white flowers are small (~3.2 mm across) with 5 petals. The petals can sometimes be of unequal size and are somewhat heart shaped.
They are deciduous trees and shrubs. The alternately arranged leaves are divided into leaflets. The inflorescence is a simple or compound raceme of many flowers. Each flower has an inflated calyx with five teeth.
Gonystylus augescens grows as a small tree. The twigs are dark brown. Fruit is ellipsoid, reddish brown, up to long. The specific epithet augescens is from the Latin meaning "elongating", referring to the inflorescence.
The leaves are up to 13 centimeters long and 1.6 wide. They are divided into many small sections. When crushed they smell like orange peels. The inflorescence is an umbel of tiny white flowers.
At the top of a 10 cm inflorescence, the flowers are over 2.5 cm, deep pink to red. The individual flowers are 5-petalled, star- shaped and have dark pink stamens and white anthers.
There are branching, coiled tendrils. The plant bears a dense inflorescence of up to 10 pea lavender- veined white flowers each up to 1.5 centimeters wide. The fruit is a hairless dehiscent legume pod.
Most of the leaves are located in a tuft about the base of the stems. The inflorescence is a thin row of V-shaped spikelets arranged parallel to and mostly flat against the stem.
Aconitum degenii is a tall spindly erect to scandent forb which is perennial from rhizomes. It has divided leaves. The flowering period extends primarily from July to September. The inflorescence is paniculate and branched.
The bark is heavily covered with long hairs. The leaves are generally three-lobed and alternately arranged. Inflorescence is racemose. The fruit is oblong and measures about 4.5 mm and 1 mm in circumference.
The inflorescence holds up to about 15 white or pinkish flowers each less than a centimeter long.Hickman, J. C. 1993. The Jepson Manual: Higher Plants of California 1–1400. University of California Press, Berkeley.
The inflorescence is a rounded head filled with leaflike green bracts deeply divided into long, narrow, pointed lobes. The small pink-tinged white to dark blue flowers are tucked amidst the spine-lobed bracts.
The linear or lance-shaped leaves are up to 3 centimeters long. The inflorescence is a cyme of bell-shaped flowers each about half a centimeter long. They are purple with whitish tubular throats.
The inflorescence bears several flowers with pinkish or greenish white tubular throats long, their bases enclosed in pointed sepals. The flower face has five mostly white lobes. The fruit is a capsule about long.
The hairy, glandular inflorescence is a one-sided curving or coiling cyme of bell-shaped flowers. Each flower is up to a centimeter long and deep to light purple to nearly white in color.
This annual herb has an erect stem reaching in maximum height. It is covered in glandular hairs. The leaf blades are somewhat rounded with toothed edges. The inflorescence is a loose cyme of flowers.
The plant features terminal inflorescence ending in white flowers that come up in summer. The chromosome number varies: 2n=16, 32, 48. The subspecies are separated geographically, generally with only one subspecies per geographic area.
The short inflorescence is tightly packed with whorls of flowers that range in color from pale blue to light lavender. As the calyces age they expand and turn pink, complementing the color of the flowers.
This perennial herb had a thick, unbranched stem up to 22 centimeters long. The inflorescence contained up to 6 bell-shaped lavender flowers. The fruit was a winged capsule up to 2 centimeters long.Calochortus indecorus.
The inflorescence is a wide, spreading array of many flower heads, each lined with green- or black-tipped phyllaries. The heads contain yellow disc florets and most have very tiny yellow ray florets as well.
Endospermum medullosum is dioecious, i.e., each tree has either male or female flowers, and therefore cannot self-fertilize. The flowers are generally small and are greenish white in color. The inflorescence type is a raceme.
The leaves are each divided into a number of leaflets up to long. The inflorescence is a dense raceme of flowers. The flowers are pink or pale purple and up to long.S.G. Aiken, et al.
The inflorescence is a cluster of leaflike green or reddish bracts strung densely with cobwebby white wool and bearing bright yellow flowers. Each flower has five rounded lobes and long, protruding stamens with large anthers.
The inflorescence is a rhipidium usually containing two flowers. The flower has six dark blue tepals each up to 2 centimeters long. The fruit is a capsule which may reach nearly a centimeter in length.
The larvae live and develop in 1–2 years. They feed on the inflorescence of the Chinese fan palm (Livistona chinensis). Adults mainly feed on rotting fruits and can be found from January to April.
This species is characterized by leaves under 5 centimeters long and 3.5 wide. The inflorescence is a spike occupying the top of the stem. The flowers have pink-tipped green sepals and tubular pink corollas.
The edges are deeply cut into narrow, sharp-pointed lobes. The inflorescence is an array of somewhat rounded flower heads surrounded by several narrow, pointed bracts with spiny edges. The head blooms in whitish petals.
This plant is a perennial herb growing up to in height. The roots are pink to reddish brown in color. The inflorescence is an umbel of tiny white flowers. Blooming occurs in July through September.
The leaves are divided into threadlike or needlelike lobes. The inflorescence is a head of flowers lined with palmate bracts. The flowers are purple and roughly a centimeter long, their corollas divided into five lobes.
The basal leaves may have toothed edges and the upper ones are smooth-edged. The inflorescence is a raceme of flowers with narrow yellow petals. The fruit is a silique a few millimeters long.Physaria hemiphysaria.
Oregon Department of Agriculture. It grows up to 90 centimeters tall from a network of tubers. The inflorescence is pyramidal, with the lower pedicels much longer than the upper. Flowering occurs in April through June.
The genus Rhynchosia (Fabaceae) in Alabama. Phytologia 91(1). The inflorescence is a raceme of up to 15 flowers. The flowers are yellow with purple or brown veining and measure up to 8 millimeters long.
The inflorescence is a series of flowers, each on a curved pedicel. The flower has small green sepals and tiny white petals. The fruit is an array of four nutlets each lined with comblike prickles.
The flowers are yellow. They form raceme inflorescence and make clusters of 3 to 9 flowers attached in a long panicle. Each flower is about 6 mm in diameter. The sepals are oval and entire.
The terminal inflorescence can have the form of a cyme or a raceme. These flower from early summer well into fall. The flowers are sessile on a flexuose arched spike. The fertile flowers are hermaphroditic.
Perennial. Base woody. Leaves in a single large basal rosette up to 1 m across; pinnatifid, wooly, with a pointy tip. Scape up to 1.5 m, without bracts. Inflorescence an umbellate group of flower heads.
The plant produces a tall inflorescence originating from the subterranean pseudobulb that continues to produce flowers over several months. The flowers are approximately one centimetre in diameter with yellow petals and brownish green striped sepals.
Inflorescence is a panicle of racemes, with many small yellow flowers.Stergios, Basil, & Berry, Paul Edward. 1996. Studies in South American Caesalipiniaceae, I, Two new species of Jacqueshuberia from the Venezuelan Guyana. Novon 6: 429-433.
It is no more than tall. Each leaf is made up of three leaflets coated in silvery hairs. The inflorescence contains 4–9 reddish purple flowers. This plant grows in pinyon-juniper and sagebrush ecosystems.
It is a compact woody shrub, average height , maximum height . The leaves are narrow, densely haired and silver green. Its flowers are pale blue to pale bluish rose and sit in an egg-shaped inflorescence.
An Encyclopedia of Cultivated Palms. Portland: Timber Press. / (page 389) All species have spines on the rachis and petiole. The monocarpic species present a Christmas tree shaped inflorescence, or instead, upward-reaching branches spreading horizontally.
At the end of each of the many branches is a tube-shaped inflorescence which opens into a tiny white or greenish-yellow flower a few millimeters wide. There are two subvarieties of C. brevicornu.
The inflorescence generally contains 2-20 flower heads per stem. Each head contains 75–150 white, lavender or blue ray florets surrounding many yellow disc florets.Flora of North America, Erigeron speciosus. Showy fleabaneEastwood, Alice 1896.
Eriogonum breedlovei is a perennial herb forming low mats of spreading stems lined with woolly oval leaves no longer than about a centimeter. The inflorescence is a cluster of tiny white to reddish, hairy flowers.
Each stem has up to 12 leaves up to long by wide. The leaves tend to roll up during dry conditions. The inflorescence is a panicle up to long. The spikelet is pale and shiny.
The inflorescence takes the form of a globular umbel of white flowers with parts in sixes. The seeds are glossy black and triangular in cross section. The average pH of an onion is around 5.5.
The leaves are about wide and hairless. Meadow foxtail has a cylindrical inflorescence with glumes about wide and spikelets about long. The ligule is long, with a slightly tattered top.BSBI Description retrieved 1 December 2010.
George placed B. aculeata in B. subg. Banksia because its inflorescence is a typical Banksia flower spike; in B. sect. Banksia because of its straight styles; and B. ser. Tetragonae because of its pendulous inflorescences.
The inflorescence consists of 14-18 chrome-yellow flowers appearing in leaf axils in upper branches. The pedicel is smooth long. The perianth pale yellowish to green and long. The style is smooth and long.
The plant blooms in an inflorescence of many white or pink flowers, each with a tube throat up to 2 centimeters long. The fruit is a winged, heart-shaped body about half a centimeter long.
Leaves are toothed with a sharp point. There are one or two inflorescence per axil with 14 to 20 flowers on each raceme. Flowers are devoid of a nectar-producing gland. The pedicels are smooth.
The inflorescence is a rounded head of tiny white flowers.USFWS. Determination of endangered status for three Puerto Rican plants. Federal Register September 9, 1994. This is a federally listed endangered species of the United States.
Fimbristylis velata is a small densely tufted annual. Its leaves are shorter than its culms. There is no ligule. The compound inflorescence has many solitary spikelets on branches which are up to 5 cm long.
They have thick, cigar-shaped pseudobulbs which are clustered. The leaves are pleated in the upper part and deciduous. The pseudobulbs become spiny after the leaves have dropped. The inflorescence is borne on the basis.
The inflorescence is a cluster of flowers accompanied by a long, cylindrical bract which appears like an extension of the stem. The flower is made up of a few pointed, brown segments with membranous edges.
A. Rhigospira quadrangularis, portion of a plant. Fig. 1, the inflorescence. Fig. 2, a flower: both natural size. Fig. 3, the corolla in bud, showing the pyramidal form of the erect segments in aestivation. Fig.
Tuberaria lignosa is a perennial herb, often woody towards the base. It reaches a height of and branches freely. Its leaves are simple, long and wide. The inflorescence is lax, with each flower in diameter.
They are most common in dry oak forests. Most species have stiff, drought-resistant leaves and large onion- shaped pseudobulbs.Dressler, R. L. The Orchids, Natural History and Classification. The flowers arise from an apical inflorescence.
This sedge is variable in appearance. In general, it forms a tuft of grasslike stems and leaves up to 80 or 90 centimeters tall. The inflorescence has staminate spikes above spikes of pistillate flowers.Carex saxatilis.
The inflorescence is up to about 25 centimeters long. The hairy spikelet is about a centimeter long not counting the long awn, which can be up to 5 centimeters long and has two distinct kinks.
They are mostly oval with smooth edges and rounded tips. The inflorescence is made up of a number of racemes of flowers. There is a white- or pinkish-flowered form and a red-flowered form.
The inflorescence is narrow and compact, bearing spikelets parallel to the stem instead of spreading outward. Each spikelet is one to two centimeters long and contains up to 14 or 15 florets with membranous margins.
The inflorescence is a raceme of flowers with four white or lavender petals each a few millimeters long. The fruit is a hairy silique 1.5 to 2 centimeters in length which contains tiny reddish seeds.
In addition, 13/98 defined fen 蕡 "Cannabis inflorescence" and 13/159 bo 薜 "wild Cannabis". Male flowers are normally borne on loose panicles, and female flowers are borne on racemes.Bouquet, R. J. 1950. Cannabis.
As in lower traps, the upper surface of the lid closely matches the exterior of the pitcher in colouration. The plant has a racemose inflorescence measuring up to 37 cm in length by 2.5 cm in diameter. The peduncle itself may be up to 18 cm long by 3 mm wide, whereas the rachis is up to 20 cm long. The inflorescence bears one-flowered pedicels (7–9 mm long), with the lowermost ones sometimes bearing a filiform bract up to around 0.5 mm long.
Outside of the "maculata group", D. majalis is very similar to D. fuchsii, but is distinguished by the following characters: the spots of the leaves are less elongated, the bracts of the inflorescence are longer and the lower transcend the inflorescence itself; it tends to be less cylindrical (a little more 'globular'), the stem is hollow (not solid) and the leaves are slightly larger. Other similar orchids are D. incarnata and D. lapponica but these species have hollow stems and different habitat (fens and bogs).
The flowers are produced on a tall spike, each flower is 3.5-4.5 cm long, zygomorphic, with two 'lips' closing the corolla tube lobed divided into three parts and is purple red, almost 5 cm long. Wild plants have pink to purple flowers, often with yellow lips. Most 8 to 30 short stalked flowers are in an inflorescence together; the inflorescence axis is glandular hairy. The crown is 25 to 45 (rarely to 70) millimeters long and in different colors (red, pink, orange, yellow, white).
The lower inflorescence bracts of S. albovaginatus do not have the marginal membranaceous extensions that are evident in S. aureus and S. triticoides. In addition, the wheat-like panicle of S. triticoides is longer than the short, compressed inflorescence of S. albovaginatus. Finally, neither S. aureus nor S. triticoides have the long perianth bristles that are present in the spikelets of S. albovaginatus. The flowering heads of S. albovaginatus resemble those of Schoenus pictus; however, the latter species lacks the membranaceous leaf sheaths present in S. albovaginatus.
Inflorescence of Campanula glomerata Campanula glomerata is a perennial herbaceous plant growing to a height of , with a maximum of . The stem is simple, erect and shortly pubescent, basal leaves are petiolated, oval-lanceolate and lightly heart- shaped (cordate), while cauline leaves are lanceolate, sessile and amplexicaul. The inflorescence is formed by 15-20 sessile, actinomorphic and hermaphrodite single flowers of about 2 to 3 cm. They are in terminal racemes or in the axils of upper leaves, surrounded by an involucre of bracts.
Occasionally, three tiny "flowers" consisting of two stamens and a pistil are produced, by which sexual reproduction occurs. Some view this "flower" as a pseudanthium, or reduced inflorescence, with three flowers that are distinctly either female or male and which are derived from the spadix in the Araceae. Evolution of the duckweed inflorescence remains ambiguous due to the considerable evolutionary reduction of these plants from their earlier relatives. The flower of the duckweed genus Wolffia is the smallest known, measuring merely 0.3 mm long.
L. nivalis also has 1–2 cauline leaves which are long; both leaf types are grass-like, flat, linear, straight and possess parallel veins. The leaf tips are obtuse, acuminate, involute, caducous and slightly swollen. Both the blade adaxial and abaxial surfaces are glabrous, with sparse, white, non-glandular hairs along the blade margins. The inflorescence of Luzula nivalis is congested in a single, dark, many-flowered head 0.8–1.0 × 0.6–0.9 cm in size; between 5–60 small flowers can be found in each inflorescence.
The taproot is large, with numerous branches extending to a depth of , with tough stems, often reddish, and unbranched until just below the inflorescence. The junctions of the petioles with the stems are covered by a sheath formed by two fused stipules known as an ocrea, a thin, paper-like membrane - a characteristic of the family Polygonaceae. The stem leaves are alternate and are narrowly ovate–lanceolate. The inflorescence consists of large clusters of racemes which contain small greenish flowers that change to red as they mature.
USDA NRCS Plant Fact Sheet. The inflorescence is a branching panicle with brown or greenish spikelets. This grass is a good forage for animals and it is sometimes added to seed mixes used for vegetating rangeland.
It is characterised by an indumentum of thick brown hairs, which is even present on the inflorescence. Pitchers are mostly green throughout with some having red blotches on the inside surfaces.Clarke, C.M. 1997. Nepenthes of Borneo.
There are four brownish red tepals (7–9 mm by 1.8–2.1 mm), and four stamens. The anther filaments are 0.7–1.5 mm long. There are 20-90 white or pale yellow flowers in an inflorescence.
The inflorescence stem has a length of 15 to 18 millimetres and a diameter of 2 millimetres. The flower stalks are 5 millimetres long.Botanical Society and Exchange Club of the British Isles 1917 . 1917, p. 617.
The inflorescence consists of 20–50 white-cream flowers on a short stem and appear in leaf axils from October to January. The fruit are smooth, egg-shaped long and wide ending with a short beak.
Vascular Plants of the Gila Wilderness The inflorescence is a series of regular bracts and tiny flowers, each five-lobed white corolla less than 3 millimeters wide. The paired nutlets are arch-shaped and not prickly.
Flora Neotropica 64: 1–112. Vegetatively, resembles E. andrieuxii, nut differs by having distinct pellucid lines, a usually paniculate inflorescence and by achenes with beaks that are at most 1/3 as long as the body.
Each is made up of a few leaflets with toothed tips. The inflorescence contains up to 11 flowers with yellow petals each about half a centimeter long.Soják, P. (2006). Two new American species of Potentilla (Rosaceae).
Possible wildfires will destroy the mature plants, but the seeds will survive such an event, retained in caps in the dried inflorescence. When released after such fires, the seeds are dispersed by means of the wind.
The yellowish-white flowers are hermaphroditic and bear many stamens; they somewhat resemble a huge pale St John's Wort flower (a distant relative among the Malpighiales). There are often two dozen or more flowers per inflorescence.
The forewings are uniformly brownish gray, with a bronzy luster. The hindwings are the same color, but lightly scaled.TOLweb The larvae feed on Yucca whipplei. They feed primarily in the apical portion of the inflorescence stalk.
This is an annual bunchgrass growing 10 to 80 centimeters tall and bearing hairy leaves up to 15 centimeters long. The inflorescence is a branching panicle up to 12 centimeters long with rounded spikelets at nodes.
The inflorescence is a compound umbel of yellow flowers with 10 to 20 rays measuring 2 to 12 centimeters long each. The fruit is somewhat rounded in shape, ribbed, and up to half a centimeter long.
The inflorescence is a solitary flower borne on a threadlike pedicel. The flower has usually five sepals and five tiny white petals. There are two subspecies which differ mainly in the microscopic appearance of the seeds.
The leaves are coated in short, rough, whitish hairs. The inflorescence is a compound umbel on a peduncle up to 3 centimeters tall. It bears several yellow flowers contained in a cuplike unit of fused bractlets.
The inflorescence is made up of a few long-haired spikelets each up to long. They are wrapped in a lance-shaped bract called a spatheole. This sheath is long and can have a sharp point.
They are held on an extremely short inflorescence. It flowers all through the year, but with a peak from February to May.JB Castillon: Aloe castilloniae, un nouvel Aloe (Asphodelaceae) du Sud-Ouest Malgache. Succulentes. 2006/3.
The species has elliptic leaf blades long by wide on petioles up to long. The inflorescence is a panicle of flowers. Each flower has a fuzzy, tubular, cream or yellowish corolla just under a centimeter long.
The branching twigs are covered in tiny linear leaves no more than 2 or 3 millimeters long. The inflorescence is a dense spike flowers 1 to 4 centimeters long. Each tiny flower has four pink petals.
Inflorescence is a small cyme frequently resembling a head, with up to 25 flowers. Flowers are 3-ribbed or slightly 3-winged. Flowers are white, about 1 mm in diameter.Godfrey, R. K. & J. W. Wooten. 1979.
The glandular inflorescence produces several tubular purple flowers up to 2 centimeters long. The mouth of each flower may be hairless or coated in long hairs, and the staminode usually has a coat of yellow hairs.
Muhlenbergia mexicana is a rhizomatous perennial herb growing 30 to 70 centimeters tall. The inflorescence is a narrow series of short, appressed to upright branches lined densely in small, pointed spikelets each a few millimeters long.
The leaves are divided into several narrow, threadlike linear lobes. The inflorescence is a woolly cluster of narrow, leaflike bracts laced with webby fibers. The small flowers have yellow throats and white or blue corolla lobes.
The bristly inflorescence is a cluster of urn-shaped manzanita flowers which are hairy inside. The fruit is a drupe just under a centimeter wide which is hairy when new and becomes hairless as it ripens.
Leaves higher on the plant are similar, but generally smaller. The inflorescence is a compound umbel of many spherical clusters of small white flowers. These yield ribbed, oblong-shaped fruits each about half a centimetre long.
This tree produces thousand of fruits, ripening three months after anthesis. The fruit matures during the rainy season, this is a deciduous, stands erect and bare before shedding large bud scales that envelops twigs and inflorescence.
It is a perennial herb. The narrowly oblanceolate-elliptic leaves are 7–20 cm long and 1.5–4 cm wide. The scape is 7–25 cm tall. The inflorescence is cylindrical and 2–10 cm long.
The inflorescence is a spiral of flowers each just over a centimeter long. They are purple in color with yellow patches on their banners. The fruit is a hairy legume pod 4 or 5 centimeters long.
The inflorescence usually consists of one or two clusters. Bracts are about , more or less round and tipped with an awn (bristle). Salvia columbariae grows tall. Its stem hairs are generally short and sparse in distribution.
The top of the stem forms an inflorescence of a few flowers, each with four bright rose-purple petals. The fruit is a flat, straight silique about 3 centimeters long which contains several oblong little seeds.
The linear or lance-shaped leaves are up to 4.5 centimeters long. The inflorescence is a rounded head of tiny white flowers.USFWS. Determination of endangered status for three Puerto Rican plants. Federal Register September 9, 1994.
The herbage is coated in silvery silky hairs. The inflorescence is a raceme of whorled yellow flowers each about a centimeter in length. The fruit is a silky-haired legume pod 3 or 4 centimeters long.
Its inflorescence is an umbel of two or more pairs of flowers, which have rusty corollas covered with dense intertwined hairs. The fruit is globular, and the bract enlarges under the fruit. The leaves are flat.
Leaves can be up to 94 centimeters long and 25 centimeters wide. Inflorescence can be 100 centimeters tall and 70 centimeters in diameter. 10 to 13 ray florets 10–13 and 25 to 50 disc florets.
The leaf blades and sheaths, which comprise the leaves can be hairless, sparsely hairy or hairy. The inflorescence is a dense or open panicle, usually drooping or nodding, sometimes spreading (as in Japanese brome, B. japonicus).
The corolla may be any of several colors from white to yellow to deep lavender and may be mottled or speckled and tinted in the throat. The inflorescence and some flower parts are glandular and hairy.
The inflorescence is a cyme of 2 to 30 flowers which are variable in color and size. Each has usually five petals up to a centimeter long which may be white to pale yellow to gold.
The brownish inflorescence is a very small, narrow terminal head, with the basal pointed, ribbed green glume the same length as the rest of the head. The fruit is an ovoid, three-sided nut in diameter.
The inflorescence produces a single flower which has an elongated, cylindrical or cone-shaped receptacle up to 3 centimeters long. At the base of the receptacle are curving, spurred sepals and three to five tiny petals.
The lower spikes are female, while the terminal spike is gynecandrous. This inflorescence is often hidden in the leaves, which form a dense tussock. The species often reproduces clonally. This sedge grows in alpine snowbed habitat.
The inflorescence is a one-sided curving or coiling cyme of many purple flowers. The North Coast variety has bell-shaped flowers under a centimeter in length, while the island variety has wider, sometimes larger flowers.
The leaves are up to 3 centimeters long and divided into threadlike lobes. The inflorescence is a head filled with palmate green bracts speckled with resin glands. The tubular purple flowers are under a centimeter long.
The bark is smooth or furrowed. The oppositely arranged, deciduous leaves are oval in shape with smooth edges. The inflorescence is a flat-topped cluster of white flowers. The fruit is a blue or purple drupe.
There may be one or more leaves on the stem as well. The erect inflorescence bears up to 30 yellow mustardlike flowers. The fruit is an oval silique up to a centimeter long containing several seeds.
Silene vallesia can reach a height of . It is a perennial pubescent sticky plant with ascending flowering stems. Leaves are oblong-lanceolate, opposite, gradually smaller, long. Inflorescence is a raceme with only 1-3 flowers, long.
Disa ferruginea is a stout, reed-like terrestrial 200–450 mm tall. Radical leaves linear, developing after flowering; cauline leaves dry, sheathing. Inflorescence dense, 1–40 flowered. Flowers bright red to orange, often with some parts yellow.
It blooms between June to September and produces an axillary or terminal raceme regular inflorescence with white or cream flowers with white or cream styles. Later it forms smooth, oblong or ellipsoidal, glabrous fruit that are long.
Their disposition can be alternate, opposite, or whorled (usually alternate except when subtending an inflorescence). Even, lamina keep entire and are setaceous or linear. The leaf just shows one vein without cross-venules. Stomata are not present.
Potentilla rimicola leaves are borne on long petioles, their palmate blades each divided into five toothed leaflets. The inflorescence is a cluster of up to 20 flowers, each with five yellow petals under a centimeter in length.
Vigna are herbs or occasionally subshrubs. The leaves are pinnate, divided into 3 leaflets. The inflorescence is a raceme of yellow, blue, or purple pea flowers. The fruit is a legume pod of varying shape containing seeds.Vigna.
This rhizomatous perennial grass forms clumps of stems up to 80 centimeters tall. The inflorescence is up to about 16 centimeters long and has erect or spreading branches with spikelets near the ends.Festuca ligulata. Grass Manual Treatment.
Retrieved 10-17-2011. The inflorescence is an umbel of flowers with purple sepals and tiny purple-striped white petals. The shiny, oval- shaped fruit is often red-tinged. It may be up to a centimeter long.
The inflorescence is a branching cluster of flowers. The plant is easily distinguished from other Schiedea on Kauai, which are not vines. This plant was thought to be extinct until it was rediscovered in 1993.Schiedea helleri.
Vulpia elliotea is an erect grass, growing up to in height. Its leaf sheaths are glabrous, and its blades are typically glabrous though they can be scabrous above. The involute blades are wide. The inflorescence is long.
Pallenis spinosa reaches on average of height. Leaves are alternate, lanceolate or elliptical. The basal ones have short petioles, while the cauline ones are sessile or semiamplexicaul. A solitary inflorescence grows at the top of the branches.
They have few leaves or many. The inflorescence is variable, bearing a single spikelet to over 100.Scleria. Flora of North America. Despite the variety, examination of the fruits and subterranean structures is required to distinguish species.
The inflorescence is a narrowed panicle up to 80 centimeters long by 17 wide. Some seed is produced but most reproduction is vegetative, with new plants sprouting from tillers and the rhizome.Panicum amarum. USDA NRCS Plant Guide.
The inflorescence is a cluster of fuzzy flower heads under a centimeter long containing long, protruding white disc florets and no ray florets. The fruit is an achene a few millimeters long with a rough bristly pappus.
The pointed, hairy leaves along the stem are up to 11 centimeters long. The inflorescence is a series of five-lobed white flowers 2 millimeters to over one centimeter wide. The fruit is a narrow, ribbed nutlet.
This medium- sized orchid is epiphytic in forest at higher elevations. It has oblong- fusiform stems (pseudobulbs) carrying deciduous, ridged, many nerved, oblong- lanceolate, acute leaves. The leaves 4–5. Inflorescence arching to horizontal, 8-10 flowered.
The inflorescence is a raceme of flowers at the tip of the stem. The mustardlike flower has four orange to bright yellow petals each up to a centimeter long. The fruit is a plump, hairy, rounded capsule.
The inflorescence is multibranched and from 200 to 400 mm long. The tightly packed flowers are unisexual and coloured lilac to pink. Male flowers are borne in pairs, and have six stamens. The female flowers are solitary.
The inflorescence is a small raceme of green or yellow-green flowers. Each has usually 3 lance-shaped sepals, 2 similar petals, and one petal known as the lip, which is longer and rounded at the end.
The flowering culms are tall. The inflorescence is an open panicle with solitary spikelets on narrow pedicels. Each spikelet has between two and six florets. The glumes have pointed tips and are narrower than the fertile lemma.
It has a long rhizome system. It has short, flat, spiral-arranged leaves. At the top of the stem is an inflorescence of ovate, pointed spikelets, each on a long peduncle. The spikelet has many hairy bracts.
Other parts of aerial pitchers are similar to their lower counterparts. Nepenthes tobaica has a racemose inflorescence. The peduncle and rachis can each grow to 20 cm in length. Partial peduncles are two-flowered and lack bracteoles.
The lid and spur are similar to those of lower pitchers. Nepenthes longifolia has a racemose inflorescence. Male and female inflorescences have the same structure. The peduncle is up to 25 cm long and 3 mm wide.
Upper pitchers also bear 14 to 18 longitudinal nerves. The mouth is horizontal and elongated into a short neck near the lid. Nepenthes ovata has a racemose inflorescence. Female inflorescences are usually slightly larger than male ones.
The paired leaves are lance-shaped and nearly 9 centimeters in maximum length. The glandular inflorescence bears blue-purple or pinkish flowers up to 4 centimeters long. The flowers have white, mostly hairless mouths and hairless staminodes.
The leaves are tiny, succulent and linear or narrowly triangular. The inflorescence is spike-like with bracts similar to the leaves, small flowers with 5 petals, 5 stamens and 2 styles. The fruiting perianth has silky wings.
The inflorescence is a small array of a few narrow branches bearing spikelets. It is an ephemeral grass, beginning to produce stems near the end of winter, flowering in early spring, dying and withering away by July.
The leaves are 1 to 3 centimeters long, widely lance-shaped and sometimes folded lengthwise. The glandular inflorescence bears tubular flowers up to 3 centimeters long. They are generally purple-blue in color, often with white throats.
At 3-4mm in size these flowers are large compared to most other genus members. In younger plants inflorescence clusters are limited to branch junctions, but in age clusters are born along the upper stem as well.
The inflorescence generally contains only 1 flower head per stem. Each head contains 15–32 blue, or white ray florets surrounding many yellow disc florets.Flora of North America, Erigeron salishii G. W. Douglas & Packer, Can. J. Bot.
The stem leaves are lanceolate and only 6 mm long and 2 mm wide. The flowering period is May to August. The loose, paniculate inflorescence contains 7 to 60 flowers. The sepals are protruding or struck back.
The species in the genus are rhizomatous perennials. The leaves are mainly basal, with a few cauline, laterally compressed, distichous and equitant at base. The culms are tufted and pithy. The inflorescence consists of several partial panicles.
The inflorescence is a head of two to ten flowers which are pinkish purple in color with paler tips. This fruit is a cylindrical legume pod up to long with a sharp, pointed beak at the end.
The inflorescence is an open array of 2 to 7 off-white to pale lilac flowers each less than a centimeter in length. The fruit is a curved, leathery, hairy legume pod up to 2 centimeters long.
Each inflorescence has 7 to 16 flowers and is located in the axil of a leaf. The flowers are small and bisexual. Sepals are completely lacking. Petals are often absent, but are small and white when present.
The inflorescence is a raceme of many flowers, sometimes arranged in whorls. Each flower is just over a centimeter long and bright yellow to orange in color. The fruit is a hairy legume pod up to long.
The male flowers are usually many per bract, the bud globose, ca. 2 mm in diameter, the petals narrow and small. The female flowers are usually solitary, at the base of the inflorescence. Flowering is Jun–Aug.
Cyperus rotundus inflorescence, Kerala Flower stem showing triangular cross-section C. rotundus has many beneficial uses. It is a staple carbohydrate in tropical regions for recent hunter-gatherers and is a famine food in some agrarian cultures.
Each palmate leaf is made up of 5 to 9 leaflets up to 5 centimeters long. The stout inflorescence bears many unwhorled flowers each around a centimeter long. The flower is partly or entirely purple in color.
The plant has an unpleasant scent. The leaves vary in shape and size, the ones higher on the stem becoming smaller. The inflorescence is a compact or spreading array of 15 to 50 or more flower heads.
The inflorescence produces hairy, glandular flower heads filled with yellow disc florets and a fringe of up to 125 thin, flat white to purple-tinged ray florets. The fruit is an achene with a pappus of bristles.
The inflorescence is a compound umbel at the top of the stem.Wolff, Karl Friedrich August Hermann. Repertorium Specierum Novarum Regni Vegetabilis 9(222/226): 421. 1911.Davidse, G., M. Sousa Sánchez, S. Knapp & F. Chiang Cabrera. 2009.
The inflorescence is an open array of flower heads amidst leaflike bracts. The flower head contains many pale violet to nearly white ray florets and a center of yellow disc florets. The fruit is a hairy achene.
The lateral inflorescence gives a raceme or a panicle with few to many miniature to small (from a few mm. to 1 cm), resupinate flowers. The distinct column has an elongate, rostellar beak. There are four pollinia.
It is a distinctive plant sending up erect red-orange stems from a gray-green basal rosette. The small yellowish-red thimble-shaped flowers top the stems in a cyme inflorescence. Some subspecies are considered threatened locally.
The inflorescence is a solitary flat-topped woolly flower head containing many yellow disc florets. There occasionally appears a yellow ray floret, but they are usually absent. The fruit is an achene with a pappus of bristles.
This species is an annual herb growing just a few centimeters tall. It is yellowish green in color. The leaves are up to 1.5 centimeters long. The inflorescence contains one or two flowers with yellow- green tepals.
Strobilanthes integrifolius is much branched shrubs, to 2 m high; stems are terete and glabrous. Leaves are opposite. It bearing blue to light violet flowers. Inflorescence simple or compound spikes, interrupted, to 10 cm long, strong- smelling.
The inflorescence is a solitary flower on a long peduncle up to 20 centimeters in length. The morning glory flower at the end is a white to pale lavender or pinkish bloom 2 or 3 centimeters wide.
The inflorescence is a dense cluster of flowers accompanied by dark-veined oval bracts. Each flower has a calyx of triangular sepals and a tubular corolla roughly long, pale brownish or pinkish in color with red veining.
They have a few wide lobes along the edges which may have teeth or smaller lobes. The leafy inflorescence bears clusters of flowers each with five wedge-shaped orange petals around a centimeter long, and yellow anthers.
They are mostly hairless, except for long hairs along the edges. The erect inflorescence bears fewer than 10 yellow mustardlike flowers. The fruit is a lance-shaped silique one or two centimeters long, containing several winged seeds.
This perennial grass grows up to 4 feet tall. The leaves are up to 12 centimeters long and are lined with silky hairs along the edges. The inflorescence is a pale green panicle with hairy spikelets.Anthaenantia villosa.
Eriocephalus africanus in flower Eriocephalus africanus after seeding Eriocephalus africanus; details of inflorescence Eriocephalus is a genus of African flowering plants in the daisy family.Linnaeus, Carl von. 1753. Species Plantarum 2: 926-927 in LatinTropicos, Eriocephalus L.
Oncidium ensatum, the Latin American orchid or Florida dancinglady orchid, is a species of orchid found in southern Florida, southern Mexico (Chiapas and the Yucatán Peninsula), Central America, Cuba, the Bahamas, and northwestern Venezuela.Kew World Checklist of Selected Plant FamiliesFlora of North America, v 26 p 648, Oncidium ensatum Biota of North America Program Oncidium ensatum is usually epiphytic but sometimes terrestrial, up to tall (not including the inflorescence). The leaves are narrowly linear to lanceolate, each up to long. The inflorescence is either arching or hanging, up to long.
Inflorescence and spathe Closed Inflorescence of Zantedeschia aethiopica Emerging leaf growth Seeds Zantedeschia aethiopica is a rhizomatous herbaceous perennial plant, evergreen where rainfall and temperatures are adequate, deciduous where there is a dry season. Its preferred habitat is in streams and ponds or on the banks. It grows to tall, with large clumps of broad, arrow shaped dark green leaves up to long. The inflorescences are large and are produced in spring, summer and autumn, with a pure white spathe up to and a yellow spadix up to long.
This is a perennial herb growing up to 15 centimeters tall and covered in a coat of ash-gray woolly hairs. The leaves are linear or narrowly lance-shaped and one or two centimeters long. The inflorescence is made up of fuzzy dull to bright reddish or purplish pink bracts between which emerge smaller yellowish to greenish flowers. The color of the inflorescence is influenced by the environment of the plant; those with more northern exposures tend to have yellowish flowers and those facing south have more reddish flowers.
It is the tallest of the Gasteria species (even larger than its close relative to the east, Gasteria excelsa), with rosettes of light-green, sharp, stiff, spotted leaves, that are up to 1 meter long. The species name "acinacifolia" means "scimitar-leaves", and refers to how the smooth adult leaves curve, and end in a sharp point. The multi- branched inflorescence is often over a meter in height, with pink flowers and appears between September and December. The inflorescence is flat-topped (unlike that of Gasteria excelsa) and has racemes that spread horizontally.
The inflorescence of H. boreale is almost identical to that of Hypericum majus, but they differ in a few key ways. These include having more oblong and blunt sepals, fewer flowered clusters that are more leafy, and more broad and round leaves. The inflorescence consists of single flowers or open clusters of a few to several flowers at the tips of stems and branches, with a pair of leaf-like bracts at the base of a flower stalk. Its flowers are yellow, and less than a quarter inch in diameter.
Inflorescence Agrostis canina is a perennial plant, with stolons but no rhizomes, and culms which grow to a height of up to . It is frequently confused with Agrostis vinealis (formerly treated as a subspecies or variety of A. canina), which grows in more upland habitats and has rhizomes rather than stolons. The leaf blades are long and wide, with an acute or acuminate ligule up to long. The plant flowers from May to July, and the inflorescence is a panicle long and up to wide, with rough branches.
In fact, when birds forage at B. prionotes, only about a quarter of all movements from inflorescence to inflorescence involve a change of plant. Geitonogamous self-pollination must therefore occur more often in this species than cross-pollination. This does not imply high rates of self-fertilisation, however, as the species appears highly self-incompatible: although pollen grains will germinate on flowers of the self plant, they apparently fail to produce pollen tubes that penetrate the style. Even where cross-pollination does occur, fertilisation rate is fairly low.
B. prionotes has cream-coloured flowers with a bright orange limb that is not revealed until the flower fully opens. Known as anthesis, this process sweeps through the inflorescence from bottom to top over a period of days, creating the effect of a cream inflorescence that progressively turns bright orange. The old flower parts fall away after flowering finishes, revealing the axis, which may bear up to 60 embedded follicles. Oval or oblong in shape and initially covered in fine hairs, these follicles are from long and wide, and protrude from the cone.
Elymus elymoides is a perennial bunch grass growing to around in height. Its erect solid stems have flat or rolled leaf blades. The inflorescence is up to long and somewhat stiff and erect, with spikelets one or two centimeters long not counting the awn, which may be 9 centimeters long and sticks straight out at maturity, making the inflorescence look like a bottlebrush (see main image), and aiding wind dispersal of the seeds. In contrast, the early-season spike is compact and reddish, as in the images at left.
The herbarium specimen Clarke, Davis & Tamin 1307 was designated as the holotype of N. jacquelineae. It consists of two sheets from two different plants: a portion of a climbing stem with an upper pitcher and a mature female inflorescence; and an immature rosette with lower pitchers and a male inflorescence. The isotype Clarke, Davis & Tamin 1307, collected at the same time as the holotype, consists of a single sheet with a fragment of a sterile climbing stem bearing two upper pitchers. Both specimens are deposited at the Herbarium of Andalas University (ANDA).
The sex of seedlings can only be determined at the first flowering, which mostly occurs after three years. The male inflorescence is built up of four to six apetalous flowers, while the female inflorescence normally consists of only one apetalous flower and contains one ovary and one ovule. Fertilization occurs solely via wind pollination, which is why male plants need to be planted near the female plants to allow for fertilization and fruit production. The oval or lightly roundish fruits grow in compact grapes varying from pale yellow to dark orange.
The flowers of this species are entirely purple, each one only fully opening after anthesis of the previous one. The inflorescence itself is racemose, and its rachis spreads outwards and forwards in a zig-zag manner from the plant, and is not thickened. The inflorescence is between 30mm to 48mm in length, bearing from between one and 22 flowers, each on pedicels (flower stems) that are between 25mm to 29mm in length. The leaves are elliptic to (ob)ovate in shape, between 13mm to 19mm in length, and up to 5mm in width.
The leaves are abaxially keeled with a glossy texture, and leaflets always occur within a single plane on either side of the rachis. Inflorescences in the genus Ravenea are always interfoliar. R. musicalis is one of seven species in the genus observed to have apparent multiple staminate inflorescences, though, like the rest of its genus, it has solitary pistillate inflorescences. Whether or not any plants in the genus Ravenea, including R. musicalis have true multiple inflorescence or false multiple inflorescence (a condensed branch system within a single prophyll) is debated.
Rhynchostylis retusa (also called foxtail orchid) is an orchid, belonging to the Vanda alliance. The inflorescence is a pendant raceme, consisting of more than 100 pink-spotted white flowers. The plant has a short, stout, creeping stem carrying up to 12, curved, fleshy, deeply channeled, keeled, retuse apically leaves and blooms on an axillary pendant to long, racemose, densely flowered, cylindrical inflorescence that occurs in the winter and early spring. It is famous for its use as an hair-ornament worn by Assamese women during folk dance Bihu on the onset of spring.
The Balanophoraceae (from the inflorescence which appears to be covered by barnacles) are a subtropical to tropical family of obligate parasitic flowering plants, notable for their unusual development and obscure affinities. The family consist of 17 genera and around 44 known species. The plants are normally found in moist inland forests growing on tree roots and have an aboveground inflorescence with the overall appearance of a fungus, composed of numerous minute flowers. The inflorescences develop inside the tuberous underground part of the plant, before rupturing it and surfacing.
The inflorescence of Lobelia telekii can grow up to tall Lobelia telekii is a species of flowering plant in the family Campanulaceae, that is found only in the alpine zones of Mount Kenya, Mount Elgon, and the Aberdare Mountains of East Africa. It occurs at higher altitudes on well-drained sloped hillsides. It is a semelparous species, putting all its reproductive effort into producing single large inflorescence up to tall, and then dying. Inflorescences of L. telekii also possesses a large pith-volume for internal water storage and marcescent foliage which could provide insulation.
The foliages of larger shrubs of both Banksia paludosa subspecies resemble those of Banksia conferta subsp. penicillata, but the latter has a wider inflorescence, and the buds are more crowded in appearance on the inflorescence before anthesis. Banksia paludosa also bears a superficial resemblance to B. oblongifolia, but the latter has a prominent midrib on the leaf underside, the new growth is covered in rusty fur, and the old spikes are bare of flowers. The latter grows on dryer rocky soils while the former grows in wetter sandy soils.
Teasels are easily identified with their prickly stem and leaves, and the inflorescence of purple, dark pink, lavender or white flowers that form a head on the end of the stem(s). The inflorescence is ovoid, long and broad, with a basal whorl of spiny bracts. The first flowers begin opening in a belt around the middle of the spherical or oval flowerhead, and then open sequentially toward the top and bottom, forming two narrow belts as the flowering progresses. The dried head persists afterwards, with the small () seeds maturing in mid autumn.
The inflorescence is a series of hairy or brush-like rectangular spikelets, occur in clusters of three, between . The grass produces relatively few viable seeds and spreads mostly by its tillers and sometimes via rhizomes. The inflorescence stalk persists after the seeds drop, sticking out of the clump of leaf blades like stiff, wavy wires. It blooms between December and January according to some sources, from May to June in the Mojave Desert according to others, and from February through June in the Mohave Desert according to others.
The inflorescence is a pendulous, solitary, interfoliar spike, unbranched, with an elongated peduncle and a tubular prophyll. The prophyll is two-keeled, short and fibrous and is much smaller than the single peduncular bract, which is deeply grooved with a long beak. The lower half of the length of the rachis is covered in triads while the top has pairs of staminate flowers which shed early, leaving the inflorescence tip bare at antithesis. The bracts around the triads are pointed and ovate; those around the pairs have longer points.
Teasels are easily identified with their prickly stem and leaves, and the inflorescence of purple, dark pink or lavender flowers that form a head on the end of the stem(s). The inflorescence is ovoid, long and broad, with a basal whorl of spiny bracts. The first flowers begin opening in a belt around the middle of the spherical or oval flowerhead, and then open sequentially toward the top and bottom, forming two narrow belts as the flowering progresses. The dried head persists afterwards, with the small () seeds maturing in mid autumn.
In many hermaphroditic species, the close physical proximity of anthers and stigma makes interference unavoidable, either within a flower or between flowers on an inflorescence. Within-flower interference, which occurs when either the pistil interrupts pollen removal or the anthers prevent pollen deposition, can result in autonomous or facilitated self-pollination. Between- flower interference results from similar mechanisms, except that the interfering structures occur on different flowers within the same inflorescence and it requires pollinator activity. This results in geitonogamous pollination, the transfer of pollen between flowers of the same individual.
The two species can be distinguished by leaf anatomy: H. forsteriana has rather flat fronds with elegantly drooping leaflets, while H. belmoreana has curved leaves with erect leaflets giving the fronds a more angular appearance. More technically, if the inflorescence is a single spike and the rachis of the leaves is arcuate, the species is H. belmoreana. If the inflorescence consists of 3 to 5 (up to a maximum of 8) spikes arising from a single broad base, and the rachis of central and lower leaves is horizontal and drooping, the species is H. forsteriana.
As the beetles home in on the inflorescence, they first move in a zig-zag pattern until they get reasonably close, when they switch to a straight-line path. The beetles may be using scent to find the inflorescence when they are far away, but once within range, they find it by means of the infrared radiation. This would account for the two different types of paths the beetles follow. Once female anthesis is nearing its end and the female flowers have been pollinated, the spathe will be fully open and male anthesis begins.
Genera such as Caryodaphnopsis and Aspidostemon that share embryological characteristics with one tribe and wood and bark characteristics or inflorescence characteristics with another tribe blur the division of these groups. All available evidence, except for inflorescence morphology and wood and bark anatomy, fails to support separate tribes Laureae and Perseeae. The tribe Cryptocaryeae is partially supported by molecular and embryological studies. Chloroplast and nuclear genomes support a tribal grouping that contains all the genera circumscribed by van der Weff and Richter (1996), as well as three additional genera.
Like some other Ambrosia, the male and female flower heads are clustered separately on the inflorescence. The female head has a single floret while the male head contains several. The fruits are contained within a spiny bur.Ambrosia linearis.
37 and is derived from the Ancient Greek words κοῖλος (koîlos, hollow) and γῠνή (gunḗ, woman), referring to the concave stigma. A few species are commonly known as "necklace orchids", because of their long, pendant, multi-flowered inflorescence.
Smaller leaves occur farther up the stem. The small inflorescence grows a few centimeters tall and bears up to 50 flowers in a flat-topped array. The flowers have cream or yellowish petals up to a centimeter long.
This is a winter- flowering annual bunchgrass approaching half a meter in maximum height. The inflorescence is a dense cylindrical panicle up to 12 centimeters long. The spikelets are yellowish, greenish, or purplish, and very narrow and pointed.
Opopanax chironium grows high. This perennial herb has a branching stem, thick and rough close to the base. Leaves are serrate, pinnate, with long petioles. It produces a large, flat, yellow inflorescence at the top of the branches.
The inflorescence is composed of up to 10 racemes, each up to 7 centimeters long. The spikelets are solitary or paired. Urochloa panicoides can be confused with Urochloa setigera, but the morphology of the spikelet is slightly different.
This plant forms small clumps of stems up to 85 centimeters tall. The stem bases and leaf sheaths are tinged maroon. The leaf blades are hairy. The inflorescence contains a terminal spike and two to three lateral spikes.
This annual herb grows up to about 40 centimeters tall with linear leaves each a few centimeters long. The inflorescence has bracts tipped in pink or reddish purple. Between the bracts appear pouched, fuzzy purplish or pink flowers.
Hypericum delphicum is a perennial herb that grows tall. The plant has an herbaceous taproot from which grow many stems. The stems lack branches below the inflorescence. The sessile leaves have an obtuse base and a rounded tip.
The inflorescence is a thyrse of flowers. The flower has a hairy, glandular calyx of sepals and a purple or reddish corolla between 1 and 2 centimeters long. The staminode is hairless. Blooming occurs in June through August.
The plant is used as a carotene-rich table vegetable in Taiwan. Javanese sometimes cook and eat the green parts and inflorescence. Vietnamese also cook the plant and sometimes add its young leaves and flower to their salads.
The leaves farther up the stem are shorter, narrower, and more shallowly lobed or unlobed. The top of the stem is occupied by a raceme inflorescence of many yellow flowers. The fruit is a silique up to long.
The inflorescence is a small spike of flowers emerging from the water surface. Inflorescences also grow on submersed sections of the stem; these are smaller and spherical. It can be difficult to distinguish from similar species of pondweed.
Dark green when mature, they turn brownish red by early fall. The inflorescence is a corymb of flowers that have white petals measuring about 4 millimeters in length. The fruit is a follicle roughly one centimeter long.Physocarpus malvaceus.
Agapanthus praecox is a variable species with open- faced flowers. It is a perennial plant that can survive up to 75 years. Its evergreen leaves are 2 cm wide and 50 cm long. Its inflorescence is in umbel.
During her graduate studies, Cotter met Kenneth Tucker. They married in 1953. Shirley Cotter Tucker earned her doctorate in botany in 1956. Her dissertation was titled Ontogeny of the Inflorescence and the Flower in Drimys winteri var. chilensis.
The inflorescence is a series of small white flowers with rounded five-lobed corollas 2 to 9 millimeters wide. The fruit is a nutlet about 2 millimeters wide with a rough, tubercled or ribbed surface visible on magnification.
The inflorescence is a series of flowers, each on a curved pedicel. The flower has small green sepals and a tiny white corolla. The fruit is an array of four flattened, slightly curving nutlets lined with thin teeth.
The inflorescence occurs in wide clusters. The flowers are usually a pale blue or lavender color, and rarely a pale rose color. The upper lip of the flower is 2-lobed. The style and stamens are slightly exserted.
The inflorescence is a dense series of clustered spikelets which are flattened and longer than wide. The plant is dioecious with male and female individuals bearing different types of flowers; the two flower types are similar in appearance.
Each inflorescence is packed with flowers, each with five tiny white petals, many whiskery stamens, and usually 5 hairy pistils. The flower parts dry and may fall away, leaving a cluster of developing fruits, follicles containing the seeds.
Agouticarpa is characterized by being dioecious, having elliptic to obovate, membranaceous stipules, male flowers in a branched dichasial or thyrse-like inflorescence, a poorly developed cup-shaped calyx, pollen grains with 3-7 apertures, and large globose fruits.
They are erect plants, usually with long taproots. The fleshy to leathery leaves form a basal rosette at the root. The basal leaves may be different from those near the inflorescence. They may or may not have stipules.
Inflorescences sometimes bear a sparse indumentum of simple hairs. Caducous brown hairs are present on developing pitchers. The stem, inflorescence and tendrils are characteristically purplish-red in most plants. The lamina is green, often with a red midrib.
Figure 26 from "The Nepenthaceae of the Netherlands Indies" showing a portion of a climbing stem with a male inflorescence (Pulle 843 bis; labelled a) and dwarf plants from the mountain top (Lam 1654; labelled b and c).
Hybridization in the Catalina Island mountain mahogany (Cercocarpus traskiae): RAPD evidence. Conservation Biology 9:1 199. The inflorescence is a cluster of up to 10 flowers which do not have petals. Plants do not always flower each year.
The inflorescence bears tubular flowers with wide mouths each divided into a double-lobed upper lip and a triple-lobed lower lip, the whole flower about a centimeter in length. It is cream-colored with dark-red lines.
Atop the stem is an inflorescence of three to seven showy red-orange flowers. Each flower is up to 4 centimeters long and trumpet-shaped, with a protruding pistil and stamens tipped with anthers covered in blue pollen.
These are especially large and noticeable on the leaf top, but occur on the bottom also. The naked bishop's cap provides low ground cover and grows to be 1/4 inch to 1½ inches tall, not counting inflorescence.
The inflorescence bears a single flower head lined with green or purplish phyllaries. The head contains many purple ray florets between 1 and 2 centimeters long around a center of yellow disc florets. The fruit is an achene.
The inflorescence is generally a cluster of glandular flower heads with black- tipped yellow disc florets and sometimes one or more tiny greenish or purplish yellow ray florets. The fruit is a flat black achene with no pappus.
The forewings are dark ashy grey and the hindwings are yellowish. The larvae feed on Achras sapota. They damage the inflorescence of their host plant, preferring to feed on set fruits rather than buds, flowers or immature fruits.
The inflorescence is a cluster of flowers on the ends of stalks. The bracts are mostly ovate with teeth or lobes but sometimes entire. Sepals are . The orange to yellow petals are generally with red to orange bases.
The leaves have thick oval or round blades up to 7 centimeters long by 6 wide. The branching inflorescence has bell-shaped involucres each containing three purple-pink flowers about a centimeter wide.Mirabilis rotundifolia. Flora of North America.
Diospyros pendula is a tree in the family Ebenaceae. It grows up to tall. The fruits are round to ovoid, up to in diameter. The specific epithet ' is from the Latin meaning "hanging down", referring to the inflorescence.
The inflorescence is up to long, bearing whorls of flowers each about long. The flower is purple-blue with a whitish patch on the banner. The fruit is a hairy legume pod up to long containing several seeds.
It is a scrambling shrub, growing to 1 m in height. The ovate leaves are 2–3 cm long and 1–1.6 cm wide. The inflorescence is less than 1 cm long, bearing 1–3 very small flowers.
This plant can be differentiated from the closely related R. indica by the differences in the two species' inflorescences. R. rotundifolia bears groups of terminal inflorescence, while R. indica has solitary flowers on the axis of the leaves.
The tip of the stem is occupied by an inflorescence of very small flowers, each with yellow petals only 1 or 2 millimeters long. The fruit is a flattened oval or diamond-shaped capsule about 4 millimeters long.
The inflorescence bears up to 30 white to yellowish flowers, each between one and two centimeters long. The fruit is an inflated legume pod drying to a papery texture. It is up to about 2.5 centimeters in length.
Jepson Manual. 1993 The stiff, short, rolling leaves are mostly located near the base of the tuft. The inflorescence has hairy spikelets which produce large awned fruits. The root system is thick and penetrates deeply into the soil.
The Nature's Calendar Survey. The inflorescence is robust and often tinged purple. It produces a large amount of seed and is a rapid coloniser of disturbed ground. It prefers wetter ground; it is often seen around drainage ditches.

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