Common Names
Click on the language to view common names.
Common Names in Chinese:
Ci Gan Ju, Tian Chun Huang Ju
Common Names in Danish:
Ager-Gåseurt
Common Names in Dutch:
Valse Kamille, Wilde Kamille
Common Names in English:
Corn Chamomile, Field Chamomile, Field Chamomile Anthemis Arvensis, Mayweed, Scentless Chamomile, Scentless Chamomile
Common Names in French:
Anthémis Des Champs, Fausse Camomille
Common Names in German:
Acker Hundskamille, Ackerkamille, Feld-Hundskamille, Hundskamille
Common Names in Hungarian:
Montika, Parlagi Pipitér
Common Names in Norwegian:
Hvit Gåseblom, Kvit Gåseblom
Common Names in Polish:
Rumian Polny, Woloweko, Zajecznik
Common Names in Portuguese:
Camomila-Do-Campo
Common Names in Romanian:
Muşeţel Prost, Mărucă, Măruncă, Mărună, Roman, Romaniţă, Romaniţă De Cîmp, Romaniţă Proastă, Romaniţă Puturoasă, Romoniţă, Romoniţă Proastă, Romăniţă De Cîmp
Common Names in Russian:
Pupavka Polevaia
Common Names in Spanish:
Manzanilla Bastarda, Manzanilla Silvestre
Common Names in Swedish:
åkerkulla
Description
Family Asteraceae
Annuals
, biennials, perennials
, subshrubs
, shrubs
, vines
, or trees
. Roots usually taproots
, sometimes fibrous
. Stems usually erect
, sometimes prostrate
to ascending
(underground stems sometimes woody caudices or rhizomes, sometimes fleshy
) . Leaves usually alternate or opposite, sometimes in basal rosettes, rarely in whorls; rarely stipulate
, usually petiolate
, sometimes sessile, sometimes with bases
decurrent onto stems; blades
usually simple
(margins
sometimes 1 2+ times pinnatifid
or palmatifid
), rarely compound
. Inflorescences indeterminate heads (also called capitula) ; each head
usually comprising a surrounding involucre of phyllaries (involucral bracts
), a receptacle, and (1 ) 5 300+ florets; individual heads sessile or each borne on a peduncle; heads borne singly or in usually determinate, rarely indeterminate, arrays (cymiform, corymbiform
, racemiform
, spiciform
, etc.
) ; involucres sometimes subtended by calyculi (sing. calyculus) ; phyllaries borne in 1 5( 15+) series proximal
to (i.e.
, outside of or abaxial
to) the florets
; receptacles usually flat to convex
, sometimes conic or columnar
, either paleate (bearing paleae or receptacular
bracts that individually subtend
some or all of the florets) or epaleate (lacking paleae) ; epaleate receptacles sometimes bristly
or hairy
or bearing subulate
enations
among the florets. Florets bisexual
, pistillate
, functionally staminate
, or neuter
(also called neutral) ; sepals highly modifed (instead of ordinary sepals, each ovary usually bears a pappus of bristles
, awns
, and/or scales
, sometimes in combination
within a single pappus) ; petals connate
, corollas (3 ) 5-merous, ± actinomorphic
or zygomorphic (one or both kinds in a single head, see descriptions
of radiate
, discoid
, liguliflorous, disciform, and radiant following) ; stamens (4 ) 5, alternate with corolla lobes
, filaments
inserted
on corollas, usually distinct
, anthers
introrse
, usually connate and forming tubes
around styles (rarely filaments connate and anthers distinct; e.g.
, Heliantheae, Ambrosiinae) ; ovaries inferior, 2-carpellate, and 1-locular with 1 basally attached, anatropous ovule
; styles 1 in each bisexual, functionally staminate, or pistillate floret; each style usually ringed at base by a nectary
, distally 2-branched with stigmatic
papillae borne on adaxial
face
of each branch
in 2 separate or contiguous
lines
or in 1 continuous band
(styles usually not branched in functionally staminate florets), style branches apically truncate
or appendaged beyond the stigmatic bands or lines, appendages
usually papillate
to hirsute
distally on abaxial (or abaxial and adaxial) faces. Fruits (technically cypselae, historically called achenes) usually dry with relatively thick, tough pericarps, sometimes beaked
(rostrate
) and/or winged
(alate
), often dispersed with aid from pappi. Seeds 1 per fruit, exalbuminous
; embryos straight.
Genera ca.
1500, species ca. 23,000 (418 genera, 2413 species in the flora
) : nearly worldwide, especially rich in numbers of species and/or in numbers of plants
in arid
and semiarid regions of subtropical
and lower to middle
temperate
latitudes
.
Asteraceae (Compositae, "composites," or "comps") have long been recognized as a natural group, and circumscription of the group has never been controversial (although some authors
have divided
the traditional family
into three or more families) . A. Cronquist (1981) placed Asteraceae as the only family in the order
Asterales within subclass Asteridae, associated with the Gentianales, Rubiales, Dipsacales, and Calycerales and relatively distant
from Campanulales. On recent molecular phylogenetic
data, the Angiosperm Phylogeny Group (2003; see references there for details; classification abbreviated
APGII hereafter) has suggested that Asteraceae are better treated as part of a more widely defined Asterales within the asterids II informal clade (or campanulid clade; see W. S. Judd and R. G. Olmstead 2004) . Judd and Olmstead summarized the higher-order relationships
of Asteraceae as follows (in order of decreasing inclusiveness; synapomorphies in parentheses) : asterids (ovules unitegmic
and tenuinucellate
, iridoid chemistry) ; core
asterids (sympetaly, stamen number equal to petal number, stamen epipetaly, mostly 2 3-carpellate gynoecia) ; campanulids (early sympetaly), comprising eight unassigned families plus Aquifoliales, which is sister to Dipsacales, Apiales, and Asterales (last three sharing frequently inferior ovaries, polyacetylenes) ; and Asterales, which appears to be sister to Dipsacales-Apiales (K
. Bremer et al.
2004) . The order Asterales (valvate
petals, lack of apotracheal
parenchyma, storage of inulin
, ellagic acid
present, and, possibly, the presence of a plunger or brush
pollen presentation
mechanism) now includes the following families (fide APGII) : Alseuosmiaceae, Argophyllaceae, Calyceraceae, Campanulaceae (optionally including Lobeliaceae), Goodeniaceae, Menyanthaceae, Pentaphragmaceae, Phellinaceae, Rousseauaceae, and Stylidiaceae. Within Asterales, Asteraceae is part of a clade (corollas with more or less fused lateral
veins joining midvein
near lobe apices, thick integuments, no endosperm haustorium) with the Menyanthaceae (cosmopolitan
with Southern Hemisphere genera) basal to a more nested clade (inferior ovaries, possibly connate anthers, pollen exine with bifurcating columellae) comprising Asteraceae, Goodeniaceae (mainly Australia), and Calyceraceae (South America), the last being the immediate sister to Asteraceae (highly modified, persistent
calyces, corolla venation
patterns
, unilocular
and uniovulate
gynoecia, pollen with intercolpar depressions
, specialized fruits) . Aggregation of flowers into heads with involucres appears to have been a parallel phenomenon in Calyceraceae and Asteraceae, given the determinate nature of the former and indeterminate (racemose) organization of the latter. Some traits
typical of Asteraceae predate evolution of the family as a distinct clade. Relationships of Asteraceae and Calyceraceae have been discussed by M.
H. G. Gustafsson and Bremer (1995) . Synapomorphies of the Asteraceae clade include: calyces modified to structures called pappi, anthers connate (forming tubes) and styles modified to function as brushes in a specialized pollen presentation mechanism, ovaries each containing a single basal ovule, and production
of sesquiterpene lactones
.
K. Bremer et al. (2004) gave an Early Cretaceous origin
for the Asteridae and the basal campanulids, and a Late Cretaceous origin for the Asterales. Bremer and M. H. G. Gustafsson (1997) also hypothesized a Late Cretaceous ancestry of Asterales in East Gondwanaland (Australasia), with later expansion into West Gondwanaland (South America-Antarctica), where the Asteraceae originated before the final separation
of South America and Antarctica. Similarly, M. L. DeVore and T. F. Stuessy (1995) argued that the close relationships of Asteraceae to Goodeniaceae and Calyceraceae, plus the basal position of Barnadesioideae K. Bremer & R. K. Jansen (Asteraceae), indicated a South America-Antarctica-Australia origin for the complex
. After reviewing previous hypotheses, they proposed a late Eocene origin for the complex and suggested a South American origin for the Asteraceae based on the basal position of the South American Barnadesioideae (see also Stuessy et al. 1996, on Barnadesioideae origin in southern South America in the Oligocene
) and their sister relationship to Calyceraceae. Fossil pollen data (both Mutisieae and Asteroideae types notably Heliantheae in the broad sense among earliest reports) reviewed by A. Graham (1996) appear to indicate an Eocene origin for Asteraceae in South America, with migration to North America at least by the Oligocene, possibly as early as the late Eocene. More recently, M. S. Zavada and S. E. de Villiers (2000; and references therein) reported Asteraceae pollen (assignable to Mutisieae in the broad sense) from the Paleocene-Eocene of South Africa, suggesting an earlier, West Gondwana (southern Africa
or Australia) origin for the family. Such data indicate that some tribes
of Asteraceae may have arrived in North America via long-distance dispersal
or island hopping well before closure
of the isthmus of Panama. They also have a bearing on the possible times of radiation
of some tribes in North America, particularly Heliantheae in the broad sense and Eupatorieae, which originated in the continent (including Mexico and parts of Central America), and those that came to North America from or through South America such as Mutisieae, Vernonieae, some Plucheeae, and Astereae. Other tribes, such as Cynareae, Cichorieae, some Gnaphalieae, and Anthemideae, may have reached North America from Eurasia
, possibly via Beringia (or as Amphi-Atlantic disjuncts
), at a later time.
The bases of a tribal classification within Asteraceae were established
in the nineteenth century, primarily through the work of H. Cassini (especially in articles scattered
through the 61 volumes of F. Cuvier 1816 1845; Cassini included
synopses of his tribes as part of his entry for Zoegea, i.e., zyégée in French; the articles have been collected in three volumes by R. M. King and H. W. Dawson 1975), C.
F. Lessing (1832), A. P. de Candolle (1828 1838, 1836 1838), and, particularly, G. Bentham (1873) . In the twentieth century, the tribal system
of Cassini, as elaborated by Bentham, was widely followed with only slight modifications (see S. Carlquist 1976; A. Cronquist 1955, 1977; C. Jeffrey 1978; G. Wagenitz 1976b; see also J. Small 1919 and, for alternate views on Heliantheae-Eupatorieae, H. Robinson 1996) .
A molecular phylogenetic study by R. K. Jansen and J. D. Palmer (1987) established that a South American clade (later named Barnadesioideae) is basal within Asteraceae. Both cladistic morphologic analyses (e.g., K. Bremer 1994, 1996) and mostly chloroplast-DNA molecular phylogenies (e.g., Jansen et al. 1991, 1992; K. J. Kim et al. 1992; Kim and Jansen 1995; R. J. Bayer and J. R. Starr 1998; P. K. Eldenäs et al. 1999; B
. G. Baldwin et al. 2002) have deepened our knowledge of tribal interrelationships within Asteraceae and led to the recent proposal
of a phylogenetic classification for the family with 10 subfamilies and 35 tribes (J. L. Panero and V. A. Funk 2002) .
Treatment of Asteraceae here differs from some of the recently proposed classifications in that some groups continue to be traditionally circumscribed (e.g., Mutisieae in the broad sense, Heliantheae in the broad sense, including Helenieae and excluding Eupatorieae) . Where appropriate and so far as practicable, new taxonomies are acknowledged in our discussions of individual tribes (which see) . In North America, the following subfamilies and tribes, as defined by J. L. Panero and V. A. Funk (2002), are represented (tribes with no native
representatives are marked
by asterisks
) : Mutisioideae-Mutisieae in the strict
sense, Gochnatioideae-Gochnatieae, and Hecastocleioideae-Hecastocleideae (all included in Mutisieae here, which see), Carduoideae (Cardueae = Cynareae), Cichorioideae (*Arctoteae, Cichorieae, Vernonieae), and Asteroideae [Senecioneae, *Calenduleae, Gnaphalieae, Anthemideae, Astereae, Plucheeae, *Inuleae, Eupatorieae, and the following segregates
of Heliantheae in the broad sense (all treated here within or as subtribes
of a fairly traditionally circumscribed Heliantheae) : Bahieae, Chaenactideae, Coreopsideae, Helenieae, Heliantheae in the strict sense, Madieae, *Millereae, Perityleae, Polymnieae, and Tageteae) ].
Asa Gray produced
the first broadly influential floristic synthesis of North American Asteraceae. Other authors who made important contributions to floristics of North American Asteraceae in the nineteenth and first half of the twentieth centuries were S. F. Blake, N. L. Britton, R. S. Ferris, M. L. Fernald, E. L. Greene, H. M. Hall, M. E. Jones, D. D. Keck, P. A. Rydberg, J. K. Small, and S. Watson. Some of those authors had narrower concepts of genera and species than had their predecessors and they freely recognized new taxa in Asteraceae (mostly genera and species) . Floristics of North American Asteraceae in the second half of the twentieth century was especially influenced by A. Cronquist (e.g., 1955, 1980, 1994; H. A. Gleason and Cronquist 1991), who usually favored traditional generic
circumscriptions.
In the last 20 years or so, developments in molecular systematics
have led to revisions
of generic limits in some tribes of Asteraceae and, sometimes, to a return to generic concepts that had been suggested earlier but largely ignored. More or less worldwide, taxonomies in some tribes or parts of tribes have included segregate genera that have been revived or newly published. Most of the innovations will be summarized in the forthcoming Asterales volume of K. Kubitzki et al. (1990+) . The generic circumscriptions adopted here incorporate recent taxonomic
findings relevant to North America, insofar as our contributors have accepted them. As a result, many of the genera treated herein have never been presented in a major flora before, and some species are included within genera with which they were not associated traditionally. Thus, the Flora brings together much new knowledge and many new names
. In most instances, circumscriptions of species have turned out to be conventional. So far as practicable, recently named species from North America have been accounted for within relevant treatments herein.
With 418 genera and 2413 species (Table
1), Asteraceae is, numerically, the largest family in the flora of North America north of Mexico. Members
of the family are found in diverse
habitats
, from the High Arctic
tundra
and polar
deserts to the Sonoran warm-desert scrub
, and from alpine
habitats to salt marshes. Asteraceae are particularly conspicuous
elements
of warm-desert and intermountain grasslands, as well as of desert scrubs, notably the intermountain desert scrub where Artemisia dominates (M. G. Barbour and N. L. Christensen 1993) . Among other conspicuous species, members of Solidago and Symphyotrichum form a very showy part of the fall
flowering in eastern North America, and members of Heliantheae sometimes produce
striking displays in the American West (e.g., Gaillardia spp.
, Lasthenia spp., members of Madiinae) .
Much has been published, not only on systematics
(at various levels), but on biology
, chemistry, and economic and medical uses of Asteraceae worldwide, particularly in proceedings (from conferences and symposia) edited by V. H. Heywood et al. (1977), T. J. Mabry and G. Wagenitz (1990), and D. J. N. Hind et al. (1995, 1996) .
Relatively few North American species of Asteraceae are economically important or widely used ethnobotanically. The only major Asteraceae crop of North American origin is the sunflower, Helianthus annuus, which is valued for its seed oil
and is appreciated in the horticultural trade. Other crop
plants from native species
worth mention are Helianthus tuberosus, the Jerusalem artichoke, and Parthenium argentatum, the guayule, a source of rubber. Echinacea spp. are touted as health plants. Members of several genera of Asteraceae native to the flora are grown for their ornamental
value, notably species of Coreopsis (tickseeds), Echinacea (coneflowers), Helianthus (sunflowers), Liatris (blazingstars and gayfeathers), Rudbeckia (black-eyed Susans), Solidago (goldenrods), and Symphyotrichum ("asters" of the trade) .
Many species of Asteraceae have been introduced
into North America, mainly from Europe and Asia, some deliberately for medicines, foods, or horticulture
, others accidentally (often with seeds or other agricultural products or by other means) . Few, if any, of the introduced taxa are thought to be noxious at the continental level, but some (e.g., Acroptilon) are considered noxious in large parts of their ranges
within the flora. Taraxacum officinale is a common lawn weed
that (in terms
of dollars spent and herbicides
applied in weed control) has an economic and ecologic impact
disproportionate to the actual harm it causes; other weedy introduced Asteraceae are of little economic consequence. Some native Asteraceae are toxic
to cattle and other livestock and are therefore considered weeds. And some native species of open habitats (e.g., Symphyotrichum pilosum) are often considered weeds because they invade fields
left fallow. Ragweeds (especially Ambrosia artemisiifolia and A. trifida) range over nearly the whole continent and their wind-blown pollens cause late-summer allergic reactions (hayfever) for a large number of people. Because ragweeds have a large impact on human health, they have a significant, negative
economic impact.
In contrast to Orchidaceae, for which a wealth of excellent, well-illustrated popular books are available, few popular field guides on Asteraceae of North America have been published. The guide
by T. M. Antonio and S. Masi (2001) deserves notice for its maps, color photographs, and useful information.
Composites
(members of Asteraceae) share some unusual morphologic traits and some morphologic terms are used in particular ways as applied here to them.
For treatments of composites here, "perennials" are herbaceous and differ from annuals and biennials in living longer
than two years and differ from subshrubs, shrubs, and trees in not developing woody aerial
stems.
In most composites, leaf venation comprises a midrib
plus more or less equal lateral nerves or veins; such leaves are described as pinnately nerved. Venation in leaf blades of some composites often consists of a midrib plus relatively strong
lateral veins that diverge at or just distal to bases of blades. Such leaves are described as 3-nerved, 3( 5) -nerved, 5-nerved, etc., and, as appropriate, the phrases "from bases" or "distal to bases" may be added for clarification.
Composites often have subsessile
to sessile or sunken
glandular
hairs
that consist of multicellular
bases supporting globular elements that usually contain resinous
or sticky substances. Such structures have been called glands
, glandular hairs, glandular trichomes, punctae, resin dots, and so on. Sometimes, the glands are embedded
in epidermal depressions or pits. Epidermes with glands more or less sunk into or embedded within the surface have been called glandular-punctate and/or punctate-glandular. The glands may be colorless (translucent
) or yellowish to dark brown or orange and are sometimes more prominent
on dried specimens than in living plants. In keys
and descriptions here, gland-dotted refers to the presence of such glandular hairs, whether sessile or in depressions or pits (as appropriate, "in pits" or "sessile" may be added for clarification) .
Inflorescences of composites are called heads (or capitula, sing. capitulum) . Heads may be borne singly (i.e., not clearly associated with other heads on the same plant) or associated in arrays. The arrays of heads on composites correspond to arrays of individual flowers (inflorescences) on plants of other families; arrays of heads are sometimes called capitulescences
. Terms for architectural
structures of arrays of heads are parallel to terms for kinds of inflorescences: cymiform, corymbiform, paniculiform
, racemiform, spiciform, thyrsiform, etc.
In radiate heads, peripheral florets (ray florets) in one or more series have corollas with zygomorphic limbs and may be pistillate, or styliferous and sterile
, or neuter; the central florets (disc florets) in radiate heads have ± actinomorphic corollas and may be bisexual or functionally staminate. In liguliflorous heads, all florets are bisexual and (usually) fertile
and have zygomorphic corollas (ligulate
florets) ; liguliflorous heads are characteristic of Cichorieae and are found in no other composites. In discoid heads, all florets have ± actinomorphic corollas and all are either bisexual and fertile or all are either functionally staminate or pistillate (in monoecious or dioecious taxa, e.g., Baccharis spp.) . In disciform heads, all florets have ± actinomorphic corollas, and peripheral florets (in one or more series) are usually pistillate and usually have relatively slender (often filiform
) corollas. Such peripheral pistillate florets are generally thought to be derived by reduction from ray florets, and plants with disciform
heads are generally thought to be derived from ancestors
with radiate heads. The central florets of disciform heads are usually bisexual, sometimes functionally staminate. By tradition and for simplicity, both the peripheral, pistillate florets and the inner, bisexual or functionally staminate florets in disciform heads may be referred to as "disc" florets. In radiant heads, all florets have ± actinomorphic corollas and the peripheral florets usually have much enlarged corollas and may be bisexual, pistillate, or neuter; the central florets of radiant heads are usually bisexual. Some composites have peripheral, bisexual florets with slightly to strongly zygomorphic corollas (e.g., some members of Chaenactis, Lessingia, Thymophylla, et al.) ; heads of such plants do not quite conform to any of the five types just described and such heads may be referred to as "quasi-radiate" or "quasi-radiant." Some florets in heads of some Mutisieae have 2-lipped corollas and those heads may be called "quasi-radiate" or "quasi-liguliflorous." The term eradiate is used to refer collectively to discoid, disciform, and radiant heads.
Heads with all florets of one sexual form (bisexual, pistillate, or functionally staminate) are called homogamous (discoid and liguliflorous heads are homogamous
, some radiant heads may be homogamous) and heads with florets of two or more sexual forms are called heterogamous (radiate and disciform heads are heterogamous, some radiant heads may be heterogamous) .
Phyllaries collectively constitute an involucre, usually number 5 21( 50+), usually are unequal (outermost usually shorter than the inner), and usually are arranged ± imbricately (overlapping like shingles) in 3 5( 15+), usually ± spiral
series. Sometimes, the phyllaries are ± equal in 1 2 series; they are rarely wanting
(e.g., Psilocarphus spp.) . Phyllaries may be herbaceous or chartaceous
to scarious
and are often medially herbaceous with chartaceous to scarious borders and/or apices. The phyllaries "proper" are sometimes immediately subtended by a calyculus (pl. calyculi) of (1 ) 3 15+ distinct, usually shorter bractlets
in 1( 3+) series (e.g., Coreopsis spp., Taraxacum spp.) .
Receptacles may bear paleae (i.e., some or all florets are individually subtended by a bractlet called a palea or receptacular bract) . Collectively paleae have been called "chaff" and paleate receptacles have been described as "chaffy." Receptacles that bear paleae are referred to as paleate and receptacles that never bear paleae are referred to as epaleate. Epaleate receptacles sometimes bear subulate enations (e.g., some Gaillardia spp.) or bristles or subulate to linear scales
(e.g., some Cynareae), or fine hairs (e.g., some Anthemideae) . Epaleate receptacles (and paleate receptacles that have shed their paleae) may be smooth
or pitted
(alveolate
, foveolate, etc.) .
The terms tube, throat, and limb have been variously used in descriptions of corollas of composites. Here, in ± actinomorphic corollas of bisexual and functionally staminate disc florets, the tube is the part of the corolla proximal to the insertion
of the staminal
filaments, and the limb is the part that is distal to insertion of the filaments. The limb comprises, proximally, the throat and, distally, the lobes. The distinction between tube and throat
hinges
on insertion of filaments, not on external morphology.
The relatively flat portion of a corolla of a ligulate floret from a liguliflorous head (i.e., members of Cichorieae) is called a ligule; it terminates in 5 teeth or lobes. The relatively flat portion of a corolla of a ray floret is called a lamina; it terminates in 0 3( 4) teeth or lobes. More or less bilabiate corollas are characteristic of some members of Mutisieae and are seldom found in members of other tribes.
Fruits of composites have been called "achenes" because they resemble true achenes. Achenes are dry, hard, single-seeded fruits derived from unicarpellate, superior ovaries. Ovaries of composites are bicarpellate
and inferior. Fruits derived from ovaries of composites are called cypselae (sing. cypsela, a term coined by C. de Mirbel in 1815) . Morphology of an ovary of a composite at flowering is often markedly different from the morphology of the mature
fruit (cypsela) derived from that ovary. References to cypselae in keys and descriptions here almost always refer to mature fruits, not to ovaries at flowering.
Shapes
of cypselae have been used in distinguishing among species, genera, and even subtribes of composites. In most composites, cypselae are ± isodiametric in cross
section
. In some composites, cypselae are characteristically ± lenticular
to elliptic
in cross section. Such cypselae are said to be compressed (or laterally flattened) if the longer axis of the cross section is ± parallel to a radius of the head (e.g., Verbesina spp.) . Cypselae are said to be obcompressed (or radially flattened) if the shorter axis of the cross section is ± parallel to a radius of the head (e.g., Coreopsis spp.) .
In composites, pappi (sing. pappus) are found where calyces are usually found on inferior ovaries; pappi have been shown to be greatly modified calyces. They show a great range of diversity
and are often diagnostic for recognition of taxa, especially at rank of genus and below. The forms of individual pappus elements intergrade
. For keys and descriptions here, the following distinctions are made: cross sections of bristles and awns are ± circular or polygonal and have the longer diameter of the cross section no more than 3 times the shorter diameter. Pappus elements with "flatter" cross sections (i.e., longer diameter more than 3 times the shorter diameter) are called scales, regardless of relative overall lengths
and widths
of the elements. As used here, "subulate scale" and "setiform scale" mean much the same as "flattened bristle" of some authors. Pliable to stiff pappus bristles with diameters less than ca. 50 µm are called fine bristles; pliable to stiff bristles with diameters 50 100 µm are called coarse
bristles. Rigid
pappus elements with ± circular or polygonal cross sections greater than 100 µm in diameter are called awns. Bristles, awns, and scales may be smooth or finely to coarsely barbed
or plumose
. A scale of a pappus may terminate in one or more bristlelike or awnlike appendages; such scales are said to be aristate.
In keys and descriptions, "pappus" and "pappi" usually refer to structures found on cypselae (mature fruits), not to "immature pappi" of ovaries at flowering. Sometimes pappi of ovaries that do not form fruits (e.g., in functionally staminate florets of some tarweeds) may be taxonomically useful and may be referred to in descriptions and keys.
Following is a synoptic key to tribes into which genera of composites of the flora area are placed. Keys to genera within each tribe will be found in the accounts of the individual tribes. Because some traits in the key to tribes and in keys to genera within tribes may be difficult to assess, we have also provided a key to artificial groups of composites and keys to genera within those artificial groups. Those keys will be found following the key to tribes.
In the following key, "radiate heads" have ray florets; "eradiate heads" lack ray florets and may be disciform, discoid, or radiant. Ray florets have zygomorphic corollas with laminae
; the laminae may be showy (as in some species of Helianthus) or inconspicuous (as in some species of Erigeron) . Usually, we have included plants with inconspicuous ray laminae in keys to genera of both radiate and eradiate groups.
Some plants have questionably paleate or epaleate receptacles. Epaleate receptacles of some plants are notably pitted and have fimbriate to deeply lacerate
pit borders
; such receptacles have sometimes been interpreted as paleate. Plants with notably lacerate pit borders are usually keyed here as both paleate and epaleate.
Some plants with pappi of conspicuous bristles often have the bristles subtended by minute, inconspicuous scales. Although such plants technically belong to groups with pappi "wholly, or partially, of awns or scales," they are usually also keyed here in groups characterized as having pappi "wholly of bristles," because the scales are easily overlooked. As well, some pappus elements are borderline between being called subulate or setiform
scales or being called "flattened bristles." Consequently, some plants that technically belong to groups with pappi of scales are keyed both in groups with pappi "wholly of bristles" and in groups with pappi "wholly, or partially, of awns or scales."[1]
Genus Anthemis
Annuals
(biennials) [perennials
, subshrubs
], mostly 5-90 cm (often aromatic
). Stems 1-5+, erect
to decumbent
, usually branched, strigillose
or strigoso-sericeous to villous
(hairs
medifixed
), glabrescent
[glabrous
or sericeous
to lanate
]. Leaves mostly cauline; alternate; petiolate
or sessile; blades
± obovate
to spatulate
, 1-3-pinnately lobed
, ultimate
margins
dentate
to lobed, faces
glabrous or strigillose to villous [glabrous or sericeous to lanate]. Heads radiate
[discoid
], borne singly or in lax
, corymbiform
arrays (peduncles sometimes clavate
and/or curved
in fruit). Involucres obconic to hemispheric
or broader, 5-13[-20] mm diam. Phyllaries persistent
, mostly 21-35+ in 3-5 series, distinct
, deltate to lanceolate, oblong
, or elliptic
, unequal, margins and apices (hyaline
and colorless or brownish [black]) scarious
. Receptacles hemispheric to narrowly conic, paleate (wholly or only distally) ; paleae ± flat, scarious to indurate
(subulate
or elliptic to obovate with mucronate
to acuminate-spinose tips
). Ray florets [0 or 2-]5-20[-30+], pistillate
and fertile
or styliferous and sterile
; corollas usually white, rarely yellow or pink, laminae
mostly oblong (tubes
sometimes hairy
). Disc florets (60-) 100-300+, bisexual
, fertile; corollas usually yellow, rarely pink, tubes ± cylindric
(usually proximally dilated
, ± spongy
in fruit, sometimes hairy, not saccate
), throats
funnelform
, lobes
5, ± triangular (abaxially minutely crested
). Cypselae obovoid
to obconic or turbinate
(circular or 4-angled in cross
section
), ribs
usually 9-10 (0) and smooth
or tuberculate
, faces glabrous (pericarps with myxogenic cells
) ; pappi 0 or coroniform
. x = 9.
Species 175: introduced
; Europe, sw Asia, n, e Africa; introduced in s Africa, Pacific Islands (New Zealand), Australia.[2]
Physical Description
Species Anthemis arvensis
Annuals (sometimes persisting), (5-) 10-30+[-80] cm, not notably
scented. Stems green or reddish, decumbent
(sometimes rooting
at nodes) or ascending
to erect
, branched mostly proximally, ±
strigoso-sericeous or villous
, glabrescent
. Leaf blades 15-35
× 8-16 mm, 1-2-pinnately lobed
(ultimate
lobes
triangular to
narrowly elliptic
or linear
). Peduncles mostly 4-15 cm (sometimes
clavate
in fruit). Involucres 6-13 mm diam., ± villous.
Receptacles paleate throughout; paleae lanceolate to oblanceolate
,
weakly navicular
(± carinate
), 3-4+ mm (including acuminate-spinose
tips
). Ray florets 5-20, pistillate
, fertile
; corollas white,
rarely tinged with pink, laminae
5-15 mm.
Disc corollas (sometimes
tinged with purple) 2-3(-4) mm. Cypselae 1.7-2+ mm, ribs
smooth
or weakly tuberculate
(sometimes separated by relatively deep furrows
)
; pappi 0 or coroniform
(0.01+ mm). 2n = 18.
Flowering May-Jul(-Sep). [source]
Anthemis arvensis is morphologically variable; it is found
throughout much of North America. [source]
Habit: Forb/herb
Flowers: Bloom Period: April, May, June, July, August, September. • Flower Color: near white, white
Size/Age/Growth
Size: 24-36" tall.
Habitat
Disturbed sites, abandoned plantings ; 10-400+ m [3].
Typically found at an altitude of 0 to 1,477 meters (0 to 4,846 feet).[4]
Biology
Reproduction
Duration: Annual
Growth
Culture: Space 15-18" apart.
Soil: Minimum pH: 6.6 • Maximum pH: 8.5
Sunlight: Sun Exposure: Full Sun .
Temperature: Cold Hardiness: Not Applicable (map)
Taxonomy
- Domain:
Eukaryota
(
)
- Whittaker & Margulis,1978
- eukaryotes
- Kingdom:
Plantae
(
)
- Haeckel, 1866
- Plants
- Subkingdom:
Viridaeplantae
(
)
- Cavalier-Smith, 1981
- Phylum:
Tracheophyta
(
)
- Sinnott, 1935 Ex Cavalier-Smith, 1998
- Vascular Plants
- Subphylum:
Euphyllophytina
(
)
- Infraphylum:
Radiatopses
(
)
- Kenrick & Crane, 1997
- Class:
Magnoliopsida
(
)
- Brongniart, 1843
- Dicotyledons
- Subclass:
Asteridae
(
)
- Takhtajan, 1967
- Superorder:
Asteranae
(
)
- Takhtajan, 1967
- Order:
Asterales
(
)
- Lindley, 1833
- Family:
Asteraceae
(
)
- Dumortier, 1822
- Sunflower Family
- Subfamily:
Asteroideae
(
)
- Tribe:
Anthemideae
(
)
- Genus:
Anthemis
(
)
- Linnaeus, Sp. Pl. 2: 893. 1753; Gen. Pl. ed. 5, 381. 1754.
- Chamomile [Greek anthemon, flower]
- Specific epithet:
arvensis
- L.
- Botanical name: - Anthemis arvensis
- Specific epithet:
arvensis
- L.
- Genus:
Anthemis
(
- Tribe:
Anthemideae
(
- Subfamily:
Asteroideae
(
- Family:
Asteraceae
(
- Order:
Asterales
(
- Superorder:
Asteranae
(
- Subclass:
Asteridae
(
- Class:
Magnoliopsida
(
- Infraphylum:
Radiatopses
(
- Subphylum:
Euphyllophytina
(
- Phylum:
Tracheophyta
(
- Subkingdom:
Viridaeplantae
(
- Kingdom:
Plantae
(
Unambiguous Synonyms
- Anthemis arvensis var. agrestis (Wallroth) De Candolle
- Chamaemelum arvense (Linnaeus) Hoffmannsegg & Link
Notes
Name
Status: Accepted Name
. Latest taxonomic
scrutiny: 15-Mar-2000
Place of publication
: Sp.
pl. 2:894. 1753
Name verified on 14-Apr-1993 by ARS Systematic Botanists. Last updated: 23-Aug-1994
Similar Species
Members of the genus Anthemis
ZipcodeZoo has pages for 503 species, subspecies, varieties, forms, and cultivars in this genus. Here are just 100 of them:
A. abagensis · A. abrotanifolia · A. abrotanifolia subsp. panachaica · A. absinthifolia · A. abylaea · A. abyssinica · A. aciphylla · A. adonidifolia · A. aeolica · A. aetnensis · A. afra · A. ageratifolia · A. agrestis · A. aizoon · A. alexandrettae · A. alpestris · A. alpina · A. altissima (Tall Chamomile) · A. altissima var. tomentella · A. amani · A. amblyolepis · A. americana · A. ammanthus · A. ammophila · A. anacyclus · A. anatolica · A. anemonifolia · A. anglica · A. anthemiformis · A. antilibanotica · A. antiochia · A. antitaurica · A. apiifolia · A. arabica · A. araboides · A. arenicola · A. argaea · A. argyrophylla · A. armeniaca · A. artemisioides · A. arvensis (Field Chamomile Anthemis Arvensis) · A. arvensis L. var. arvensis L. (Field Chamomile) · A. arvensis incrassata · A. arvensis subsp. cyllenea · A. arvensis subsp. glabra · A. arvensis subsp. sphacelata · A. arvensis var. arvensis (Corn Chamomile) · A. arversis · A. asperula · A. atlantica · A. atrata · A. aurea · A. auriculata · A. australis · A. austriaca (Austrian Chamomile) · A. austro-iranica · A. barrelieri · A. 'Beauty of Grallagh' · A. biaristata · A. biebersteiniana (Golden Marguerite Anthemis Biebersteiniana) · A. biebersteinii · A. blancheana · A. 'Blomit' · A. boissieri · A. bornmuelleri · A. bourgaei · A. bourgei · A. boveana · A. brachmannii · A. brachycarpa · A. brachycentros · A. brevifolia · A. bulgarica · A. buphthalmoides · A. cairica · A. calabrica · A. calcarea · A. callieri · A. 'Cally Cream' · A. 'Cally White' · A. candidissima · A. canescens · A. carpathica · A. carpatica · A. carpatica 'Karpatenschnee' (Snow Carpet Marguerite) · A. carpatica pyrethriformis · A. carpatica 'Snow Carpet' (Snow Carpet Snowy Marguerite Anthemis Carpatica) · A. carpatica subsp. petraea · A. carpetana · A. cassia · A. caucasica · A. chamomilla · A. chevalieri · A. chia · A. chrysantha · A. chrysocephala · A. chrysoleuca · A. ciliata · A. cinerea · A. clausonis
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Further Reading
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- Abhandlungen der Naturhistorischen Gesellschaft zu Nrnberg. Nrnberg: Conrad Geiger, 1852- GER url p. 139, p. 139.
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- Acta Soc. pro Fauna et Flora Fennica. Helsinki, Societas. ENG url p. 108, p. 131, p. 140, p. 144, p. 256, p. 34, p. 35, p. 42, p. 49, p. 50, p. 52, p. 55, p. 62, p. 82, p. 83.
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- An illustrated flora of the northern United States, Canada and the British possessions: from Newfoundland to the parallel of the southern boundary of Virginia, and from the Atlantic Ocean westward to the 102d meridian / by Nathaniel Lord Britton and Hon. New York: C. Scribner's sons, 1913. ENG url p. 516, p. 517.
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- Flora Scotica; or, A description of Scottish plants, arranged both according to the artificial and natural methods. London, Printed by R. and A. Taylor, for A. Constable, 1821. ENG url p. 244, p. 247.
- Flora Vectiana; being an arrangement of the more rare and interesting plants indigenous to the Isle of Wight. London, Printed by Richard Taylor, 1823. ENG url p. 32.
- Flora de las Islas Baleares, seguida de un diccionario de los nombres baleares, castellanos y botánicos de las plantas espontáneas y de las cultivadas. Palma, P. J. Gelabert, 1879-1881. SPA url p. 616.
- Flora de las islas Baleares, seguida de un diccionario de los nombres baleares, castellanos y botánicos, de las plantas espontáneas y de las cultivadas. Palma, Estab. tip. de P.J. Gelabert, 1870-1881. SPA url p. 616.
- Flora del Modenese e del Reggiano / dei Professori G. Gibelli e R. Pirotta. Modena: Tip. di G.T. Vincenzi, 1882. ITA url p. 92.
- Flora dell'isola di Pantelleria. Firenze, M. Ricci, 1922. ITA url p. 47.
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- Flora der Umgebung Lemsals und Laudohns; zwei Beiträge zur Flora Livlands, von A. Rapp. Hrsg. und mit einer phytogeographischen Einleitung versehen von J. Klinge. Riga, W.F. Häcker, 1895. GER url p. 28, p. 67.
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- Flora hibernica: comprising the flowering plants, ferns, Charace, Musci, Hepatic, Lichenes and Alg of Ireland: arranged according to the natural system with a synopsis of the genera according to the Linnan system / by James Townsend Mackay. Dublin: W. Curry jun., 1836. ENG url p. 152.
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- Flora of Illinois, containing keys for the identification of the flowering plants and ferns, by George Neville Jones Notre Dame, Ind., The University Press, 1945. ENG url p. 265.
- Flora of Indiana, by Charles C. Deam. Indianapolis, Wm. B. Burford printing co., contractor for state printing and binding, 1940. ENG url p. 989.
- Flora of Lancaster County; being descriptions of the seed- plants growing naturally in Lancaster County, Pennsylvanial. By John Kunkel Small and Joel Jackson Carter. New York, 1913. ENG url p. 308.
- Flora of Middlesex County, Massachusetts, by L. L. Dame and F. S. Collins. Malden, Middlesex Institute, 1888. ENG url p. 54.
- Flora of Pennsylvania. Edited with the addition of analytical keys by John Kunkel Small. Boston, Ginn & Co., 1903. ENG url p. 336.
- Flora of West Virginia, by Charles Frederick Millspaugh and Lawrence William Nuttall. Chicago, 1896. ENG url p. 232, p. 232.
- Flora of southeastern Washington and adjacent Idaho, by Charles V. Piper and R. Kent Beattie Lancaster, Pa., Press of the New era printing company, 1914. ENG url p. 263.
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- Flora of the northwest coast, including the area west of the summit of the Cascade Mountains, from the forty-ninth parallel south to the Calapooia Mountains on the south border of Lane County, Oregon. By Charles V. Piper and R. Kent Beattie. Lancaster, Pa., Press of the New Era Printing Company, 1915. ENG url p. 380.
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- Flora padovana; ossia, Prospetto floristico e fitogeografico delle piante vascolari indigene inselvatichite o largamente coltivate crescenti nella provincia di Padova; con notizie storico-bibliografiche sulle fonti d Padova, Prem. Soc. coop. tip., 1909-1914. ITA url p. 675, p. 749.
- Flora piacentina; ossia, Enumerazione sistematica delle piante della provincia di Piacenza, coll'indicazione delle loro stazioni, dei caratteri principali di ciascuna famiglia, dei nomi italiani, di quelli del dialetto Piacenza, Tip. F. Solari, 1877. ITA url p. 188.
- Flora uruguaya; enumeración y descripción breve de las plantas conocidas hasta hoy y de algunas nuevas que nacen espontaneamente y viven en la República Uruguaya. Montevideo, 1901- SPA url p. 500.
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- Flora von Brixen a. E.; ein mit Standorts- und Höhenangaben versehenes Verzeichnis der im weiteren Gebiete von Brixen a. E. (Südtirol) beobachteten wildwachsenden höheren Sporen- und Samenpflanzen, der Nutzgewächse und Zierg Wien, Deuticke, 1911. GER url p. 282.
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- Flora von Schaffhausen / bearbeitet von Jakob Meister. Schaffhausen: Buchdr. von H. Meier, 1887. GER url p. 107.
- Flora von Schlesien, preussischen und österreichischen Antheils, oder, Vom oberen Oder- und Weichsel-Quellen-Gebiet. Nach natürlichen Familien, mit Hinweisung auf das Linnéische System. Breslau, F. Hirt, 1857. GER url p. 257.
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- Flora von Tirol. Ein Verzeichniss der in Tirol und Vorarlberg wild wachsenden und häesiger gebauten Gefässpflanzen. Mit Berücksichtigung ihrer Verbreitung und örtlichen Verhältnisse verfasst und nach Koch's Synopsis d von Frz. Freih. v. Hausmann. Innsbruck, Wagner, 1851. GER url p. 1247, p. 1443, p. 456.
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- Flore de la Côte-d'Or: avec déterminations par les parties souterraines / par Ch. Royer. Paris: F. Savy, 1881-1883. FRE url p. 360.
- Floristicka istrazivanja po jugoistocnoj hrvatskoj. U Zagrebu, Tisak Kr. Zemaljske Tiskare, 1915. SCR url p. 16, p. 39.
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Notes
Contributors
- "Anthemis arvensis". in Flora of North America Vol. 19, 20 and 21 Page 535, 538. Published by Oxford University Press. Online at EFloras.org.
- Bisby, F.A., Y.R. Roskov, M.A. Ruggiero, T.M. Orrell, L.E. Paglinawan, P.W. Brewer, N. Bailly, J. van Hertum, eds (2007). Species 2000 & ITIS Catalogue of Life: 2007 Annual Checklist. Species 2000: Reading, U.K.
- Global Biodiversity Information Facility. Accessed January 24, 2008. http://www.gbif.org Mediated distribution data from 2 providers.
- USDA, ARS, National Genetic Resources Program. Germplasm Resources Information Network - (GRIN) [Online Database]. National Germplasm Resources Laboratory, Beltsville, Maryland. URL (April 25, 2008)
Data Sources
Accessed through GBIF Data Portal November 12, 2007:
- Jyväskylä University Museum - The Section of Natural Sciences, Vascular plant collection of Jyvaskyla University Museum
- Natural History Museum, University of Oslo, Vascular Plant Herbarium, Oslo
- Natural History Museum, University of Oslo, Vascular Plants, Field notes, Oslo
- Oregon State University, Vascular Plant Collection
- The Danish Biodiversity Information Facility, Botany registration database by Danish botanists
- The Swedish Museum of Natural History
- , Botany
- The Swedish Museum of Natural History
- , Herbarium of Oskarshamn
- The Swedish Museum of Natural History
- , Lund Botanical Museum
- The Swedish Museum of Natural History
- , Plants
- UK National Biodiversity Network, Botanical Society of the British Isles - Vascular Plants Database
- USDA PLANTS, USDA PLANTS Database
Identifiers
- Biodiversity Heritage Library NamebankID: 2657791
- Catalogue of Life Accepted Name Code: ITS-36331
- Global Biodiversity Information Facility Taxonkey: 13838352
- Globally Unique Identifier: urn:lsid:ipni.org:names:177158-1
- GRIN Nomen Number: 103870
- Integrated Taxonomic Information System (ITIS) Taxonomic Serial Number (TSN): 36331
- Natural Heritage Network Species Identifier: PDAST0J021
- U.S.D.A. Plant Symbol: ANARA2
- Zipcode Zoo Species Identifier: 19658
Footnotes
- Theodore M. Barkley, Luc Brouillet, John L. Strother "Asteraceae". in Flora of North America Vol. 19, 20 and 21 Page 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 16, 70. Oxford University Press. Online at EFloras.org. [back]
- Linda E. Watson "Anthemis". in Flora of North America Vol. 19, 20 and 21 Page 14, 487, 537, 547, 548. Oxford University Press. Online at EFloras.org. [back]
- "Anthemis arvensis". in Flora of North America Vol. 19, 20 and 21 Page 535, 538. Oxford University Press. Online at EFloras.org. [back]
- Mean = 160.080 meters (525.197 feet), Standard Deviation = 215.170 based on 3,661 observations. Altitude information for each observation from British Oceanographic Data Centre. [back]
