Antirrhinum majus

Intermediate inheritance of flower colour due to incomplete dominance[5]

It is an herbaceous perennial plant, growing to 0.5–1 m tall, rarely up to 2 m. The leaves are spirally arranged, broadly lanceolate, 1–7 cm long and 2-2.5 cm broad. The upper glandular stalk is stalk-round, sometimes woody to the middle. The opposite leaves are simple, elliptic or ovate to broad-lanceolate, sometimes linear and usually bleak. Leaflets are missing.[6]

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 "maw" of the crown is closed by protuberance of the lower lip, one speaks here of "masked", and everted baggy at the bottom. There is a circle with four stamens. The plants are pollinated by bumblebees, who are strong enough to gently and briefly open male flowers to enter and exit them without difficulty, collecting pollen in the process. A snapdragon's calyx is up to 8 mm long, with sepals of equal length, oblong to broad.

The ovary is supreme. The fruit is an ovoid capsule 10–14 mm diameter shaped like a skull,[7] containing numerous small seeds. [8]

Antirrhinum majus

Antirrhinum majus subsp. linkianum

Snapdragon -- Antirrhinum majus (cultivar) with buds with glandular hairs

Four former subspecies are now considered as separate species:[9]

• Antirrhinum majus subsp. cirrhigerum (Ficalho) Franco: now classified as Antirrhinum cirrhigerum (Welw. ex Ficalho)
• Antirrhinum majus subsp. linkianum (Boiss. & Reut.) Rothm: now classified as Antirrhinum linkianum Boiss. & Reut.
• Antirrhinum majus subsp. litigiosum (Pau) Rothm.: now synonymised with Antirrhinum barrelieri Boreau
• Antirrhinum majus subsp. tortuosum (Bosc) Rouy: now classified as Antirrhinum tortuosum Bosc ex Lam.

It is native to from southern-central France, and the eastern Pyrenees to north-eastern Spain and the Balearic Islands. They often grow in crevices and walls.[10]

A peloric snapdragon

Antirrhinum majus can survive a certain amount of frost, as well as higher temperatures, but does best at 17–25 °C (63–77 °F). Nighttime temperatures around 15–17 °C (59–63 °F) encourage growth in both the apical meristem and stem.[1] The species is able to grow well from seeds, flowering quickly in 3 to 4 months. It can also be grown from cuttings.[11]

Though perennial, the species is often cultivated as a biennial or annual plant, particularly in colder areas where it may not survive the winter. Numerous cultivars are available, including plants with lavender, orange, pink, yellow, or white flowers, and also plants with peloric flowers, where the normal flowering spike is topped with a single large, symmetrical flower.[8][12] The cultivars ’Floral Showers Deep Bronze’[13] and ‘Montego Pink’[14] have gained the Royal Horticultural Society’s Award of Garden Merit.

The trailing (creeping) variety is often referred to as A. majus pendula (syn. A. pendula, A. repens).

It often escapes from cultivation, and naturalised populations occur widely in Europe north of the native range,[8] and elsewhere in temperate regions of the world.[2]

Past common names for Antirrhinum majus include: great snapdragon, lion's-mouth, rabbit's mouth, bonny rabbits, calf-snout, toad's mouth, bulldogs, and lion's-snap.[15]

In the laboratory it is a model organism,[16] for example containing the gene DEFICIENS which provides the letter "D" in the acronym MADS-box for a family of genes which are important in plant development. Antirrhinum majus has been used as a model organism in biochemical and developmental genetics for nearly a century. Many of the characteristics of A. majus made it desirable as a model organism; these include its diploid inheritance, ease of cultivation (having a relatively short generation time of around 4 months), its ease of both self-pollination and cross-pollination, and A. majus's variation in morphology and flowering color. It also benefits from its divergence from Arabidopsis thaliana, with A. thaliana's use as a common eudicot model, it has been used to compare against A. majus in developmental studies.[1]

Studies in A. majus have also been used to suggest that, at high temperatures, DNA methylation is not vital in suppressing the Tam3 transposon. Previously, it was suggested that DNA methylation was important in this process, this theory coming from comparisons of the degrees of methylation when transposition is active and inactive. However, A. majus's Tam3 transposon process did not completely support this. Its permission of transposition at 15 °C and strong suppression of transposition at temperatures around 25 °C showed that suppression of the transposition state was unlikely to be caused by the methylation state.[17] It was shown that low temperature-dependent transposition was the cause of the methylation/demethylation of Tam3, not the other way around as previously believed. It was shown in a study that decreases in the methylation of Tam3 were found in tissue that was still developing at cooler temperatures, but not in tissue that was developed or grown in hotter temperatures.[18]

Antirrhinum majus has also been used to examine the relationship between pollinators and plants. With debate as to the evolutionary advantages the conical-papillate shape of flower petals, with arguments suggesting the shape either enhanced and intensified the color of the flower or aided in orienting pollinators through sight or touch. The benefit that A. majus brought was through an identification of a mutation at the MIXTA locus that prevented this conical petal shape from forming. This allowed testing of the pollination plants with and without conical petals as well as comparisons of the absorption of light between these two groups. With the MIXTA gene being necessary in the formation of conical cells, the use of the gene in breeding of Antirrhinum was crucial, and allowed for the tests which showed why many plants produced conical-papillate epidermal cells.[19]

Another role A. majus played in examining the relationship between pollinator and plant were in the studies of floral scents. Two of A. majus's enzymes, phenylpropanoids and isoprenoids, were used in the study of its floral scent production and the scent's effect on attracting pollinators.[1]

Antirrhinin is an anthocyanin found in A. majus.[20] It is the 3-rutinoside of cyanidin. Its active ingredients include mucilages, gallic acid, resins, pectin and bitters. It is a topical emollient, antiphlogistic, astringent, antiscorbutic, hepatic and diuretic. It is effective against inflammations, it is used for haemorrhoids. It has been used in gargles against ulcerations of the oral cavity. Internally, it can be used for colitis and heartburn. Externally, as poultices, on erythemas.

Antirrhinum majus may suffer from some pests and diseases.

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  Close-up view of Antirrhinum majus
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  White snapdragon flower
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  Yellow snapdragon flower
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  Pink snapdragon flower
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  White snapdragon flower
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  Yellow snapdragon flower
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  Bunch of pink snapdragon flowers
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  Antirrhinum majus flower