' original description (1753)|alt=First page of Linnaeus' 1753 description of Viola
History First formally described by
Carl Linnaeus in 1753 with 19 species, the genus
Viola bears his
botanical authority, L. When
Jussieu established the hierarchical system of families (1789), he placed Viola in the
Cisti (rock roses), though by 1811 he suggested Viola be separated from these. However, in 1802
Batsch had already established a separate family, which he called Violariae based on Viola as the
type genus, with seven other genera. Although Violariae continued to be used by some authors, such as
Bentham and Hooker in 1862 (as Violarieae), most authors adopted the alternative name Violaceae, first proposed by
de Lamarck and
de Candolle in 1805, and
Gingins (1823) and
Saint-Hilaire (1824). However de Candolle also used Violarieae in his 1824
Prodromus.
Phylogeny Viola is one of about 25 genera and about 600 species in the large
eudicot family
Violaceae, divided into subfamilies and tribes. While most genera are
monotypic,
Viola is a very large genus, variously circumscribed as having between 500 and 600 species. Historically it was placed in subfamily Violoideae, tribe Violeae. But these divisions have been shown to be artificial and not
monophyletic.
Molecular phylogenetic studies show that
Viola occurs in Clade I of the family, as
Viola,
Schweiggeria,
Noisettia and
Allexis, in which
Schweiggeria and
Noisettia are monotypic and form a sister group to
Viola.
Subdivision Viola is a large genus that has traditionally been treated in
sections. One of these was that of
Gingins (1823), based on stigma morphology, with five sections (
Nomimium,
Dischidium,
Chamaemelanium,
Melanium,
Leptidium). The extensive taxonomic studies of
Wilhelm Becker, culminating in his 1925 conspectus, resulted in 14 sections and many infrasectional groups. The largest and most diverse, being section
Viola, with 17 subsections. In addition to subsections,
series were also described. Alternatively, some authors have preferred to subdivide the genus into subgenera. Subsequent treatments were by Gershoy (1934) and Clausen (1964), using subsections and series. These were all based on morphological characteristics. Subsequent studies using
molecular phylogenetic methods, such as that of Ballard et al. (1998) have shown that many of these traditional divisions are not
monophyletic, the problem being related to a high degree of
hybridization. In particular section
Nomimium was dismembered into several new sections and transferring part of it to section
Viola. Section Viola
s. lat. is represented by four sections,
Viola sensu stricto,
Plagiostigma s. str.,
Nosphinium sensu lato. and the
V. spathulata group. In that analysis, the S American sections appear to be the
basal groups, starting with
Rubellium, then
Leptidium. However, the exact phylogenetic relationships remain unresolved, as a consequence many different taxonomic nomenclatures are in use, including groupings referred to as
Grex. Marcussen et al. place the five S American sections,
Andinium,
Leptidium,
Tridens,
Rubellium and
Chilenium at the base of the phylogenetic tree, in that order. These are followed by the single Australian section,
Erpetion, as sister group to
Chilenium, the northern hemisphere sections and finally the single African section,
V. abyssinica. These sections are morphologically, chromosomally, and geographically distinct.
Sections Seventeen sections are recognized, listed alphabetically (approximate no. species); • Sect.
Andinium W.Becker (113) S America • Sect.
Chamaemelanium Ging.
s.lat. (61) N America, northeast Asia (includes
Dischidium,
Orbiculares) • Subsect.
Chamaemelanium • Subsect.
Nudicaules • Subsect.
Nuttalianae • Sect.
Chilenium W.Becker (8) southern S America • Sect.
Danxiaviola W. B. Liao et Q. Fan (1) China • Sect.
Delphiniopsis W.Becker (3) western Eurasia: southern Spain; Balkans • Sect.
Erpetion (Banks) W.Becker (11–18) eastern Australia; Tasmania • Sect.
Leptidium Ging. (19) S America • Sect.
Melanium Ging. (125) western Eurasia (pansies) • Sect.
Nosphinium W.Becker
s.lat. (31–50) N, C and northern S America; Beringia; Hawaii • Sect. nov. A (
V. abyssinica group) (1–3) Africa: equatorial high mountains • Sect. nov. B (
V. spathulata group) (7–9) western and central Asia: northern Iraq to Mongolia • Sect.
Plagiostigma Godr. (120) northern hemisphere (includes
Diffusae) • Grex Primulifolia • Sect.
Rubellium W.Becker (3–6) S America: Chile • Sect.
Sclerosium W.Becker (1–4) northeastern Africa to southwestern Asia • Sect.
Tridens W.Becker (2) southern S America • Sect.
Viola s.str. (
Rostellatae nom. illeg.) (75) northern hemisphere (violets) (includes
Repentes) • Subsect.
Rostratae Kupffer (W.Becker) • Subsect.
Viola • Sect.
Xylinosium W.Becker (3–4) Mediterranean region
Species The genus includes
dog violets, a group of scentless species which are the most common
Viola in many areas, sweet violet (
Viola odorata) (named from its sweet scent), and many other species whose common name includes the word "violet". But not other "violets": Neither
Streptocarpus sect. Saintpaulia ("African violets",
Gesneriaceae) nor
Erythronium dens-canis ("dogtooth violets",
Liliaceae) are related to
Viola.
List of selected species Section
Danxiaviola •
Viola hybanthoides Section
Delphiniopsis •
Viola cazorlensis •
Viola delphinantha •
Viola kosaninii Section
Erpetion •
Viola banksii – Australian native violet, ivy-leaved violet •
Viola hederacea – Australian native violet, ivy-leaved violet Section
Leptidium ''|alt=Viola stipularis •
Viola stipularis Section
Melanium (pansies) ''|alt=Flowers of Viola tricolor •
Viola arvensis – field pansy •
Viola bicolor •
Viola pedunculata – yellow pansy,
Pacific coast. •
Viola bertolonii •
Viola calcarata •
Viola cheiranthifolia – Teide violet •
Viola cornuta •
Viola lutea •
Viola tricolor – wild pansy, heartsease Section
Nosphinium ''|alt=Flowers of Viola pedata •
Viola pedata Section A (
V. abyssinica group) ''|alt=Flower of Viola abyssinica •
Viola abyssinica Section B (
V. spathulata group) •
Viola spathulata Section
Plagiostigma ''|alt=Flower of Viola epipsila •
Viola epipsila Section
Rubellium •
Viola capillaris •
Viola portalesia •
Viola rubella Section
Sclerosium •
Viola cinerea Section
Tridens ''|alt=Flowers of Viola tridentata •
Viola tridentata – mountain violet Section
Viola (violets) ''|alt=Flowers of Viola sororia •
Viola canina – heath dog violet •
Viola hirta – hairy violet •
Viola labradorica – alpine violet •
Viola odorata – sweet violet •
Viola persicifolia – fen violet •
Viola riviniana – common dog violet •
Viola rostrata – long-spurred violet •
Viola sororia – common blue violet, hooded violet Section
Xylinosium ''|alt=Flower of Viola decumbens •
Viola decumbens Evolution and biogeography One
fossil seed of †
Viola rimosa has been extracted from
borehole samples of the
Middle Miocene fresh water deposits in
Nowy Sącz Basin,
West Carpathians,
Poland. The genus is thought to have arisen in South America, most likely the Andes.
Genetics Habitat fragmentation has been shown to have minimal effect on the genetic diversity and gene flow of the North American woodland violet
Viola pubescens. This may be partially attributed to the ability of
Viola pubescens to continue to persist within a largely agricultural matrix. This trend of unexpectedly high genetic diversity is also observed in
Viola palmensis, a Canary Island endemic known only from a 15 square kilometer range on
La Palma island. High levels of genetic diversity within these species indicate that these plants are outcrossing, even though many violet species can produce many clonal offspring throughout the year via cleistogamous flowers. Plants that produce copious amounts of clonal seeds from cleistogamous flowers often experience increased levels of inbreeding. These reportedly high rates of outcrossing and genetic diversity indicate that these violets are strong competitors for pollinators during the early spring when they are in bloom and that those pollinators can travel considerable distances between often fragmented populations. ==Distribution and habitat==