Tripleurospermum inodorum |
Tripleurospermum |
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corn scentless-chamomile, false mayweed, false-chamomile, matricaire inodore, scentless chamomile, scentless mayweed |
mayweed |
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Habit | Annuals (sometimes biennials or perennials), (5–)30–60(–80) cm. | Annuals, biennials, or perennials, 5–80 cm (taprooted; scentless or nearly so). | ||||
Stems | 1, ascending to erect, usually branched distally, sometimes proximally, glabrous or glabrate (sparsely hairy when young). |
1–5+, usually erect or ascending, sometimes procumbent, branched or simple, glabrous or sparsely hairy (hairs basifixed). |
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Leaves | blades 2–8 cm, ultimate lobes filiform, 4–20 mm, not fleshy, apices apiculate. |
(not marcescent) basal (usually withering by flowering) and cauline; petiolate or sessile; blades oblong, 1–3-pinnately lobed, ultimate margins crenate or serrate, faces glabrous or sparsely hairy. |
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Involucres | hemispheric to patelliform, 8–12+ mm diam. |
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Receptacles | convex to conic (± solid), epaleate. |
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Ray florets | 10–25; corollas (4–)10–13(–20) mm. |
[0] 10–34+, pistillate, fertile; corollas white [seldom pinkish], laminae mostly oblong. |
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Disc florets/ |
1–2.5 mm. |
300–500, bisexual, fertile; corollas yellow [greenish], tubes cylindric (sessile-glandular), throats narrowly campanulate (cylindric or compressed), lobes 5, deltate (with resin sacs). |
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Phyllaries | centrally dark greenish or brownish, oblong, subequal, scarious margins colorless to light brown, 0.1–0.2 mm wide. |
persistent, 28–60+ in 2–5 series, distinct, broadly ovate, unequal to subequal, margins and apices (pale to dark brown or black) narrowly to widely scarious (abaxial faces glabrous). |
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Heads | (1–)10–200+, 3–4.5 cm diam., in corymbiform arrays of solitary heads at ends of branches. |
radiate [discoid or disciform], borne singly or in corymbiform arrays. |
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Cypselae | pale brown, ribs separated by 1/3+ their widths, abaxial-apical resin glands ± circular, faces minutely roughened between ribs. |
trigonous, ± compressed (apices truncate), ribs 3–5 (0–2 abaxial, 2 lateral, 1 adaxial, usually whitish, relatively thick, smooth), faces often rugose or tuberculate abaxially and between ribs and glabrous (pericarps sometimes with myxogenic cells and usually 2–3, sometimes 1–5, abaxial-apical resin sacs; embryo sac development tetrasporic); pappi 0 [coroniform or each an adaxial auricle]. |
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x | = 9. |
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2n | = 18, 36. |
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Tripleurospermum inodorum |
Tripleurospermum |
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Phenology | Flowering May–Sep. | |||||
Habitat | Fields, dry shorelines, waste places | |||||
Elevation | 0–1500+ m (0–4900+ ft) | |||||
Distribution |
AK; AL; CA; CO; CT; IA; ID; IL; KS; KY; MA; MD; ME; MI; MN; MO; MT; ND; NE; NH; NJ; NV; NY; OH; OR; PA; SD; UT; WA; WI; WY; AB; BC; MB; NB; NL; NS; NT; ON; PE; QC; SK; YT; Greenland; Pacific Islands (New Zealand) [Introduced in North America; also introduced in Europe]
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North America; Eurasia; North Africa; one species widespread as a weed [Introduced in New Zealand] |
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Discussion | Tripleurospermum inodorum has been classified as a noxious weed (class C) in the state of Washington and is considered invasive in other states (it is resistant to some herbicides); it is a weed of cereals in western Canada. W. L. Applequist (2002) has shown that the name Matricaria inodora is not a superfluous new name for M. chamomilla as earlier stated by S. Rauschert (1974). Therefore, the appropriate name under Tripleuro-spermum is T. inodorum. She also considered its type to belong in T. maritimum and formally recognized it there as subsp. inodorum, on the basis of hybridization with other T. maritimum subspecies (A. Vaarama 1953); on the same basis, however, Hämet-Ahti maintained the species distinction between T. inodorum and T. maritimum, while making T. phaeocephalum a subspecies of the latter. Q. O. N. Kay (1994), in a more extensive review of the literature and of hybridization data, also maintained T. inodorum and T. maritimum as distinct species, a conclusion followed here. From the standpoint of weed science, taxonomic merging of T. inodorum and T. maritimum has the inconvenience of grouping under a single specific name taxa that have different physiologies, ecologies, weed potentials, and, possibly, reactions to weed control measures. The name Matricaria inodora var. agrestis Weiss was not validly published. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Species ca. 40 (2 in the flora). Tripleurospermum often has been included within Matricaria. It is distinguished from the latter by 3-ribbed cypselae with 2 abaxial-apical resin sacs versus 5-ribbed cypselae without apical sacs, and by production of 7-glycoside flavonols versus 3-glycosides (K. Bremer and C. J. Humphries 1993). C. Oberprieler (2001) showed that Tripleurospermum is closely related to Anthemis in the strict sense and not to Matricaria. This is supported by the tetrasporic embryo sac shared by Tripleurospermum and Anthemis (versus monosporic in Matricaria and other anthemid genera), similarity of karyotype, and the presence in both genera of matricaria ester in the polyacetylene pathway, otherwise unknown in the tribe. Although W. L. Applequist (2002) favored a single species, Tripleurospermum maritimum, for the three taxa (as subspecies) present in North America, based in large parts on the findings of A. Vaarama (1953) on crossing ability among these taxa, on the existence of hybrid populations, and on the (mistaken) supposition that they form a polyploid series, some recent authors (e.g., Q. O. N. Kay 1976b, 1994; A. R. Clapham et al. 1987; E. G. Voss 1972–1996, vol. 3) have maintained two species based on morphologic characters, notably perennial versus annual habit, spacing of ribs (closer versus wider), elongate versus ± circular resin sacs on cypselae, relative infrequency of hybrid populations, and relative sterility of some hybrid individuals, as well as both species harboring diploid and tetraploid populations (Clapham et al.; Kay 1994). Success in interbreeding among plants does not always indicate conspecific status. In North America, authors such as M. L. Fernald (1950) and H. A. Gleason and A. Cronquist (1991) treated (in Matricaria) T. inodorum and T. maritimum subsp. maritimum as a single species with varieties or as a single entity, resulting in confusion about the distinctness of the two taxa in their ranges of introduction, and also difficulty in recognizing the presence of T. inodorum in areas where T. maritimum subsp. maritimum is present in coastal northeastern United States (e.g., D. W. Magee and H. E. Ahles 1999). N. N. Tzvelev (2002b) segregated the subspecies of T. maritimum as species; under his scheme, three species are present in North America: T. inodorum, T. maritimum in the strict sense, and T. hookeri (= T. maritimum subsp. phaeocephalum). Pending further taxonomic work on this complex, I have here retained the taxonomy (except generic assignment) adopted by Kay (1976b), with two species, one including two subspecies. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 19, p. 549. | FNA vol. 19, p. 548. | ||||
Parent taxa | Asteraceae > tribe Anthemideae > Tripleurospermum | Asteraceae > tribe Anthemideae | ||||
Sibling taxa | ||||||
Subordinate taxa | ||||||
Synonyms | Matricaria inodora, Chamomilla inodora, M. maritima subsp. inodora, M. maritima var. inodora, M. perforata, T. maritimum subsp. inodorum, T. perforatum | |||||
Name authority | (Linnaeus) Schultz-Bipontinus: Tanaceteen, 32. (1844) | Schultz-Bipontinus: Tanaceteen, 31. (1844) | ||||
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