Myriophyllum quitense |
Myriophyllum ussuriense |
|
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Andean water-milfoil, waterwort milfoil, waterwort water-milfoil |
Russian water-milfoil, terrestrial water milfoil, Ussurian milfoil, Ussurian water-milfoil |
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Habit | Herbs monoecious, aquatic or semiaquatic, often forming dense stands. | Herbs usually dioecious, rarelymonoecious, aquatic or semiaquatic, usually not forming dense stands. |
Stems | often branched, to 3 m. Turions absent. |
often branched, to 0.6 m. Turions present, ± brown, narrowly cylindrical, with gradual transition from foliage leaves to highly reduced turion leaves, (4–)7–12(–20)× 0.5–2(–3) mm, apex rounded to truncate; leaves often pectinate proximally and entire to 3-fid distally, strongly appressed to axis, lanceolate to narrowly elliptic or ovate in outline, (1.5–)2–4(–6.5) × (0.2–)0.3–2(–2.5) mm; segments 0–6(–10), longest segment 0.5–2 mm, basal segment less than or equal to 1/2 central axisof leaf, apex ± acute or rounded, brown, long-necked, ascidiate trichomes in axils present. |
Leaves | mostly in whorls of (3 or)4(or 5), sometimes opposite to subopposite, heteromorphic; petiole 0–4 mm; submersed leaves pectinate to lobed (basalmost leaves opposite to subopposite, reduced, margins entire), ovate to obovate in outline, (3–)5–25(–35) × (2–)3–18(–20) mm, segments (2 or)3–9(–11), linear, ± applanate, longest segment (7–)8–15(–17) mm; emersed leaves pinnatisect to lobed or entire, ovate to oblong in outline, 2–9 × 1–6 mm, margins dentate to minutely serrate. |
opposite or in whorls of 3(or 4), heteromorphic; petiole 0–9 mm; submersed leaves usually pectinate, sometimes 2- or 3-lobed, ovate to widely ovate or trullate in outline, (1.3–)5–22(–26) × (0.3–)3–28(–35) mm, segments(0–)4–12(–14), distinctly alternate, lobed to linear-filiform, longest segment (0.5–)2–20(–25) mm; emersed leaves usually linear, spatulate, or 2- or 3-lobed, sometimes pectinate proximally, (1.7–)2.5–9(–10.5) × 0.3–3.5(–5) mm, segments (0–)2–8(–12), lobed to linear-filiform. |
Inflorescences | to 8 cm; flowers proximally pistillate, medially bisexual, distally staminate; bracteoles cream, deltate, 0.5–1 × 0.2–0.6 mm, margins dentate to serrate, with glandular tip. |
to 12 cm; flowers usually unisexual, rarely bisexual; bracteoles cream to stramineous, lanceolate, elliptic, ovate, or obovate, (0.2–)0.3–0.7(–0.9) × (0.1–)0.2–0.4(–0.5) mm, margins entire, irregular, dentate, glandular, or lobed. |
Staminate flowers | sepals green to cream, ovate to deltate, (0.2–)0.3–0.5(–0.7) × (0.1–)0.2–0.4(–0.5) mm; petals persistent, ± purple, oblong, 2–3 × 0.5–1.5 mm; stamens 8, filaments to 0.6 mm, anthers 1.8–2.5 × 0.2–0.6 mm. |
sepals cream, elliptic to lanceolate, 0.5–0.7 × 0.2–0.5 mm; petals persistent, cream, sometimes apically suffused with purple, widely oblanceolate, 1.2–2.5 × 0.7–1.2 mm; stamens 8, filaments to 1.4 mm, anthers 0.9–1.8 × 0.2–0.4 mm. |
Pistillate flowers | sepals cream, deltate, 0.2–0.5 × 0.1–0.4 mm; petals ± persistent, cream, ± cucullate, elliptic, 0.1–0.5 × 0.2–0.3 mm; pistils 1.1–2.2 mm, stigmas cream to ± purple, to 0.6 mm. |
sepals and petals rudimentary or absent; pistils to 0.7 mm, stigmas white, to 0.3 mm. |
Fruits | cylindric to oblong, 4-lobed. |
subglobose, 4-lobed. |
Mericarps | tan to olive-brown, cylindric to ovoid, 1.5–1.8 × 0.6–0.8 mm, transversely elliptic, abaxial surface rounded, smooth, sometimes with a shallow, longitudinal ridge, wings and ribs absent. |
brown, obovate, 0.8 × 0.6 mm, abaxial surface rounded, minutely tuberculate, wings and ribs absent. |
2n | = 42. |
= [14] 21. |
Myriophyllum quitense |
Myriophyllum ussuriense |
|
Phenology | Flowering Jun–Aug. | Flowering and fruiting Jul–Nov. |
Habitat | Cold oligotrophic waters, lakes, rivers, streams. | Streams, rivers, muddy shorelines of ponds and lakes, intertidal wetlands. |
Elevation | 0–2800 m. (0–9200 ft.) | 0–600 m. (0–2000 ft.) |
Distribution |
AZ; CA; ID; MT; OR; UT; WA; WY; BC; NB; PE; s Mexico; South America
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OR; WA; BC; Eurasia
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Discussion | The most distinguishing feature of Myriophyllum quitense is the production of relatively large, ovate distal floral bracts with serrate margins. This characteristic is shared only with M. heterophyllum; however, M. quitense has eight stamens and the latter has four. The proximal submersed leaves of most Myriophyllum species are uniformly pectinate, but those of M. quitense can range from entire or lobed to pectinate. This species often exhibits a pronounced transition from three or four proximal nodes of large, opposite, spatulate or lobed prophylls, to nodes of besomiform whorled leaves having obtriangular laminar surfaces and distal pinnatifid segments resembling those of pectinate leaves. In addition, the unusual grayish blue color of the foliage and whitish rhizomes are useful characteristics for distinguishing submersed vegetative specimens of M. quitense from similar species, such as M. sibiricum. Myriophyllum quitense has a highly disjunct distribution in North America and South America (A. E. Orchard 1981; O. Ceska et al. 1986). S. G. Aiken (1981) and R. Couch and E. Nelson (1988) suggested that M. quitense was introduced into North America by migratory waterfowl. Both Ceska et al. and M. L. Moody and D. H. Les (2010) regarded it as native to North America. It has been reported from New Brunswick and Prince Edward Island (D. F. McAlpine et al. 2007) and further range extensions would seem likely given the level of disjunction in distribution. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Plants of Myriophyllum ussuriense typically grow in a semi-terrestrial habit in shallow water or on saturated sediments to a height of 20 cm. Shoots often have swollen stem bases that taper dramatically towards the apex. In some populations, extensive production of erect shoots from rhizomes produce dense stands. The floral bracts are distinctive, being opposite or alternate and elongate with usually 2–8 relatively short segments. Dimorphism in size between staminate and pistillate flowers of M. ussuriense is distinctive. Although most populations appear to be unisexual with staminate plants predominating and pistillate plants rare (O. Ceska et al. 1986), the latter are extremely small with a vestigial perianth and are easily overlooked, indicating that monoecy may be more common than thought in this species. S. Ueno and Y. Kadono (2001) reported that seven of 80 populations of M. ussuriense in Japan had some monoecious plants. No fruit was found despite an extensive examination of available material. Submersed plants have pectinate leaves that are extremely delicate with usually fewer than 12 straight segments. A useful characteristic of some leaves is that the central axis terminates in a right-angled bifurcation. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 10. | FNA vol. 10. |
Parent taxa | Haloragaceae > Myriophyllum | Haloragaceae > Myriophyllum |
Sibling taxa | ||
Synonyms | M. elatinoides | M. verticillatum var. ussuriense |
Name authority | Kunth in A. von Humboldt et al.: Nov. Gen. Sp. Pl. 6(fol.): 71; 6(qto.): 89. (1823) | (Regel) Maximovicz: Bull. Acad. Imp. Sci. Saint-Pétersbourg 19: 182. (1873) |
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