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Canberra, Aust Capital Terr, Australia
Scientific Name
Matthiola incana (L.) R.Br.
Synonyms
Cheiranthus albus Mill., Cheiranthus annuus L., Cheiranthus coccineus Mill., Cheiranthus incanus L., Cheiranthus fenestralis L., Cheiranthus graecus Pers., Cheiranthus hortensis Lam., Cheiranthus viridis Ehrh., Hesperis fenestralis (L.) Lam., Hesperis incana (L.) Kuntze, Matthiola annua (L.) Sweet, Matthiola fenestralis (L.) R.Br., Mathiolaria annua (L.) Chevall.
Family
Brassicaceae
Common/English Names
Brampton Stock, Common Stock, Gillyflower, Hoary Stock, Imperial Stock, Stock, 10-Week Stock
Vernacular Names
Czech: Fiala Šedivá
Eastonian: Aedlevkoi
Esperanto: Matiolo Nuda
Finnish: Tarhaleukoija
French: Giroflée, Mattiole Blanchâtre, Voilier Grisâtre
German: Garten-Levkoje, Weisslichgraue Levkoje
Hungarian: Kerti Viola, Nyári Viola, Szagos Viola
Peru: Alhelí (Spanish)
Polish: Lewkonia Letnia
Portuguese: Goiveiro-Encarnado, Goivo-Encarnado
Slovašcina: Fajgelj, Šeboj, Sorta’
Slovencina: Fiala Sivá
Swedish: Gillyflower, Lövkoja
Turkey: Yalancı Şebboy
Welsh: Murwyll Coesbren, Murwyll Lledlwyd
Origin/Distribution
It is native to the coastal areas of southern and western Europe and has naturalized elsewhere. It has been introduced into the New World and Australia.
Agroecology
Matthiola incana is a cool climate species, growing best in temperatures of 15–24 °C. It thrives in full sun to light shade and grows best in well-drained, moist, fertile, organic rich soil with a neutral or slightly alkaline pH range.
Edible Plant Parts and Uses
Its flowers are eaten as a vegetable or used as a garnish, especially with sweet desserts (Tanaka 1976; Facciola 1990). Studies reported that M. incana seeds contained oil rich (55–65 %) in omega-3 linolenic acid and could replace marine oils and thereby contribute beneficially to the human diet (Yaniv et al. 1999).
Botany
A biennial or perennial tomentose herb, 15–75 cm high, unbranched or with sparingly basal branching. Basal leaves rosulate; cauline leaves shortly petiolate or sessile, oblanceolate, 3–16 cm long, (0.5-) 1–2 cm broad margin entire; base attenuate to cuneate, apex rounded (Plates 1 and 2). Racemes 10–30-flowered. Flower: sepals linear-lanceolate to narrowly oblong, 10–15 by 2–3 mm; petals purple, violet, pink, red or white (Plates 1, 2 and 3), obovate to ovate, 20–30 by 7–15 mm, long clawed, apex rounded or emarginate; stamens 7–9, filaments 5–8 mm, anthers 2–4 mm; style 1–5 mm, stigma bilobed, erect, sessile. Siliquae (7-) 10–15 cm long, 2.5–4 mm wide, pubescent-glandular. Seed sub-orbicular, 2 mm across, brown, winged.
Plate 1
Purple flower stock and leaves
Plate 2
Maroon flower stock and leaves
Plate 3
Bunch of stock flowers
Nutritive/Medicinal Properties
Phytochemicals in Flowers
The flavonoid glycoside dactylin with the structure 5,7,3,4′- tetrahydroxy-3′-methoxyflavone-3-O-B-d-glucopyranoside was isolated from M. incana (Rahman and Khan 1962). The following phenolic compounds p-coumaric, caffeic, ferulic and sinapic acids and kaempferol and anthocyanin pigments were found in the flowers of healthy and virus-infected plants of Matthiola incana (Feenstra et al. 1963). In healthy red flowers larger amounts of cinnamic acids were present, bound to the acylated anthocyanins and other compounds and possibly also as free acids. When anthocyanin synthesis was blocked, the formation of cinnamic acids was also inhibited, except for small amounts of sinapic and ferulic acids. In anthocyanin-producing flowers of Matthiola incana, the presence of naringenin, naringenin 7-glucoside, dihydrokaempferol and dihydrokaempferol 7-glucoside was detected (Forkmann 1979). The four isolated compounds initiated anthocyanin synthesis after administration to acyanic flowers of genetically defined lines of Matthiola incana and Antirrhinum majus.