Commelina communis the Asiatic dayflower, is an herbaceous annual plant in the dayflower family. It gets its name because the blooms last for only one day. It is native throughout much of East Asia and northern parts of Southeast Asia. In China, the plant is known as yazhicao (), roughly translating to "duckfoot herb", while in Japan it is known as , meaning "dew herb". It has also been introduced to parts of central and southeastern Europe and much of eastern North America, where it has spread to become a noxious weed. It is common in disturbed sites and in moist soil. The flowers emerge from summer through fall and are distinctive with two relatively large blue petals and one very small white petal.
The Asiatic dayflower plant serves as the type species for its large genus. Linnaeus picked the name Commelina in honour of the two Dutch botanists of the Commelijn family, using the two large showy petals of Commelina communis to symbolise them. Linnaeus described the species in the first edition of his landmark work, Species Plantarum, in 1753. Long before the plant was studied in Europe, however, it had been used for generations in traditional Chinese medicine. The flowers have also been used in Japan to produce a dye and a pigment that was used in many world-renowned Ukiyo-e woodcuts from the 18th and early 19th centuries. In the modern era the plant has found limited use as a model organism in the field of plant physiology due to its complex pigment chemistry and the ease of viewing its stomata.
The Asiatic dayflower is considered a weed both in areas where it was introduced and in certain parts of its native range. The flowers' interactions with pollinators have been well studied and have helped to support important hypotheses about pollination in the field of plant ecology. Recent research has also revealed that the Asiatic dayflower can bioaccumulate a number of metals, making it a candidate for revegetating and essentially cleaning spoiled copper mines. Several animals and fungi use the plant as a food source, with a few species feeding upon it exclusively.
Description
The Asiatic dayflower is an annual herb with stems that are typically decumbent, meaning that they are prostrate at the base but become erect towards the tips, but some individuals may be simply erect. The diffusely branched stems tend to root at the basal nodes. The pubescence on the stems is variable, but common patterns include a line of hair continuous with the leaf sheath, or they may be glabrous basally, meaning hairless, and puberulent towards the extremities, that is covered with fine hairs. The leaves are sessile: they lack a leaf stalk, also known as a petiole; or they may be subpetiolate, meaning they have very small petioles. The leaf sheaths are cylindrical, sometimes striped with red, and typically glabrous, but usually have margins that are puberulent or pilose, meaning lined with fine, soft hairs. The leaf blades range from narrowly lanceolate, or lance-shaped, to ovate–elliptic, between egg-shaped and ellipse-shaped. They measure by wide. The blades range from glabrous to puberulent and have scabrescent, or slightly rough, margins. Their tips are acute, meaning they come to a point quickly, to acuminate, meaning the point develops gradually. The leaf bases are oblique, or uneven.
The flowers are arranged on inflorescences called cincinni (singular: cincinnus), which are also called scorpioid cymes. This is a form of a monochasium where the lateral branches arise alternately. The cincinni are subtended by a spathe, a modified leaf. The solitary spathes usually measure long, but some may be up to in length, while they are tall, but sometimes up to . The uncurved spathes typically have a cordate, or heart-shaped, whitish base, which contrasts with its dark green veins. Their margins lack hairs, are somewhat scabrous, or rough, and are unfused, meaning they are distinct to the base. Their apices are acute to acuminate while the surfaces are glabrous, puberulent, or hirsute–ciliate, meaning with longer, shaggier hairs. The spathes are borne on peduncles, or stalks, that measure and sometimes up to long.
There are often two cincinni present, though the upper, or distal, cincinnus may be vestigial. The lower, or proximal, cincinnus bears 1 to 4 bisexual flowers and is nearly included in the spathe, while the upper cincinnus has 1 to 2 male flowers and is about long. The individual flowers are subtended by bracteoles that fall off early in development. The pedicels supporting single flowers, and later the fruits, are erect initially but curve when in fruit. They measure about . The 3 concave, membranous sepals are inconspicuous, but persist after the fruit develops; the lateral pair are fused basally, measure only long by wide, and are elliptic and glabrous. The lower sepal is lanceolate and about long by about wide. The 2 upper petals are blue to indigo in colour, while the much smaller lower petal is white. The upper two petals measure long by wide, while the lower petal is long by about wide. The 2 upper petals are composed of a claw about long and a broadly ovate limb with an acute apex and a cuneate-cordate base.
There are three anticous fertile stamens, meaning they are on the lower part of the flower, and three posticous infertile stamens, meaning they are on the upper part of the flower. These infertile stamens are termed staminodes. The fertile stamens are dimorphic: the lateral pair have maroon to indigo anthers that measure about long and are elliptic with a base that is sagittate or arrowhead-shaped. Their filaments are about long. The central fertile stamen has a yellow, elliptic anther with a maroon connective and a base that is hastate or spearhead-shaped, but with the lobes at right angles. The anther measures about long while its filament is about long. The three staminodes are all alike with yellow, cruciform, or cross-shaped, antherodes that are about long on filaments about long. Sometimes the antherodes will have a central maroon spot. Each antherode has two abortive lateral pollen sacks. The ovary is ellipsoid, about long and has a style that is about long.
The fruit is a dehiscent, ellipsoid capsule with two locules each containing two seeds. The capsule is glabrous, brown, measures long, and dehisces into two valves. The seeds are brown or brownish yellow in colour and deltoid, or roughly triangular in outline. They are dorsiventral, meaning they have distinct upper and lower surfaces, with the ventral, or lower, surface being planar and the dorsal, or upper, surface being convex. Seeds range in length from , but seeds as short as can occur, while they are across. The surfaces are rugose pitted-reticulate and are densely covered with smaller farinose granules with sparse larger farinose granules.
Taxonomy Commelina communis was first described in 1753 by Carl Linnaeus in the first edition of his Species Plantarum, along with eight other species in the genus. The plant serves as the type species for the genus. The scientific name Commelina was chosen based on the Asiatic dayflower. Linnaeus picked the name in honour of the Dutch botanists Jan and Caspar Commelijn, using the two large showy petals of Commelina communis to symbolise them. A number of names given to plants thought to be different species have fallen into synonymy with the Asiatic dayflower. Albrecht Wilhelm Roth created the first such synonym, Commelina polygama, in 1790. Wenceslas Bojer described what he believed were two new species, Commelina barabata and Commelina salicifolia, in his work Hortus Mauritianus, both of which were quickly found to be identical to C. communis. Karl Sigismund Kunth created the synonym Commelina willdenowii in 1841. Finally, Korean populations of the species were named under the synonym Commelina coreana in 1910 by Augustin Abel Hector Léveillé.
Several varieties have also been named. Commelina communis var. ludens was created by C.B. Clarke after demoting it from the full species status in which it was placed by Friedrich Anton Wilhelm Miquel in 1861. The variety is distinguished by its darker flowers, antherodes with central maroon spots, less well developed distal cymes that usually do not produce a flower, and spathes that are proportionally broader. Jisaburo Ohwi's Flora of Japan also treats the variety as geographically distinct, stating that it is restricted to mountainous areas. This variety is still accepted by some workers, but others, such Robert B. Faden, consider it impossible to consistently separate from the type variety. Another variety, C. communis var. hortensis, which was named by Tomitaro Makino and is apparently a cultivated variety which originated from C. communis var. ludens in Japan, is also accepted by some botanists. It differs in having larger showy flowers which are used to produce a dye (see "Uses" section below). A variegated form called C. communis var. ludens f. aureostriata named by Frank C. MacKeever in 1961 is known to occur randomly throughout much of the species' range.
Distribution and habitat The plant's native distribution includes much of East Asia and Southeast Asia. Country by country, it is found in China, Taiwan, Japan, Korea, the Russian Far East, Cambodia, Laos, Malaysia, Thailand, India, Iran and Vietnam. Within China it is found in all provinces except Qinghai, Hainan, Xinjiang, and Tibet. In Japan the plant is found throughout the bulk of the country from Hokkaido south to Kyūshū. In Russia the Asiatic dayflower is found naturally on Sakhalin as well as in the Far East in areas surrounding the Ussuri River.
The species has been introduced to much of Europe and eastern North America. On the former continent it is now found from Central Europe well into western Russia. Specifically it is known from Italy north to Switzerland, east through the region encompassing the former Yugoslavia, east into the regions around the Black Sea including Romania, the Moldavia Region, and Ukraine but excluding Crimea, north through the Dnieper Basin into Belarus and Russia, continuing east into the regions surrounding the Don River and the Volga River south to their intersection at the Volga–Don Canal and north to the regions around Lake Ladoga and Lake Ilmen, and farther east to the regions of the Ural River and the Kama River. It is also found in the Czech Republic and Slovakia. It is present in the provinces of Ontario and Quebec in Canada, and in most of the eastern and central American states from Massachusetts and New York state in the northeast, west to Minnesota and south through the Great Plains to Texas and east to Florida in the United States.
Within its native distribution, the plant is most typical of moist, open places, including shady forest edges and wet areas of crop fields, orchards, ditches, and roadsides. In Taiwan, it can be found from elevation. In areas where the Asiatic dayflower is an introduced weed it is most common in waste places, but also along the edges of fields, woods, and marshes, and occasionally penetrating into woods.
Ecology
The Asiatic dayflower is considered an invasive weed in many areas where it has been introduced. In the United States, the Virginia Department of Conservation and Recreation, for example, categorises the species as "occasionally invasive" in its Invasive Plant Species of Virginia. This means that the plant will "not affect ecosystem processes, but may alter plant community composition by outcompeting one or more native plant species". The species is typically limited to disturbed sites, whence it spreads relatively slowly. Within its native range in China it is also sometimes considered a pest, especially in the northeast of the country where it has caused economically significant agricultural damage in orchards.