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Andean water-milfoil, waterwort milfoil, waterwort water-milfoil

American milfoil, common water milfoil, myriophylle de sibérie, northern milfoil, northern water-milfoil, short-spike water-milfoil, Siberian water-milfoil

Habit Herbs monoecious, aquatic or semiaquatic, often forming dense stands. Herbs monoecious, aquatic, often forming dense stands.
Stems

often branched, to 3 m. Turions absent.

usually unbranched, to 6 m. Turions present, ± dark green, cylindrical, with gradual transition from foliage leaves to reduced turion leaves, 12–40(–45) × (3–)5–12(–15) mm, apex ± rounded;

leaves pectinate, stiff, strongly appressed to axis distally, not proximally, elliptic in outline, 5–15 × 1.4–5 mm, with clusters of brown, conical trichomes between leaf bases;

segments 13–15(–17), elongate botuliform, longest segment 1.8–5.2(–6) mm, basal segment usually less than or equal to 1/2 central axis of leaf, apex apiculate, with single, brown, conical trichome in each axil.

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.

in whorls of (3 or)4, heteromorphic;

petiole 0–4 mm; submersed leaves pectinate, usually obovate in outline, (2.8–)13–32(–44) × (2.1–)16–35 mm, segments 6–18(–24), linear-filiform, often perpendicular to central axis, basal segments often as long as leaf axis, segments often irregular in orientation, not parallel and not in same plane, longest segment 2–20(–26) mm; emersed leaves, basal sometimes pectinate to pinnatifid proximally, with abrupt transition to obovate, elliptic, sometimes distally spatulate, in outline, margins of distal leaves entire to serrate to shallowly lobed, 1–2.3 × 0.6–1(–1.5) mm.

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 15 cm;

flowers proximally pistillate, medially bisexual, distally staminate;

bracteoles cream to stramineous or purple with distinct, reddish or brown margin, usually ovate to depressed-ovate, sometimes elliptic to triangular, (0.4–)0.6–1.3 × 0.3–0.7 mm, margins entire or serrate, sometimes with distal, irregular, membranous fringe.

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 to stramineous, usually depressed-ovate, sometimes ovate to triangular, 0.2–0.4 × 0.2–0.5 mm;

petals caducous, cream to red or dark purple, oblong to elliptic or obovate, 1.7–2.3(–3) × 1–2 mm;

stamens 8, filaments to 1.5 mm, anthers greenish cream to yellow or purple, 1–2.2 × 0.3–0.7 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 cream to green to purple, lanceolate to deltate or ovate, 0.1–0.3 × 0.1–0.2 mm;

petals often persistent, cream, widely ovate, 0.3–0.5 × 0.2–0.5 mm;

pistils 1–2 mm, stigmas white to red or ± purple, ± pulvinate, 0.2–0.4 mm.

Fruits

cylindric to oblong, 4-lobed.

globose, 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.

olive-green to brown, cylindric to narrowly ovoid, 1.5–2.7 × 1.2–1.6 mm, transversely widely obovate, abaxial surface broadly rounded, sparsely and irregularly tuberculate, margins smooth or tuberculate, sometimes with 2 shallow, partial, longitudinal ridges, wings and ribs absent.

2n

= 42.

= 42.

Myriophyllum quitense

Myriophyllum sibiricum

Phenology Flowering Jun–Aug. Flowering and fruiting May–Oct.
Habitat Cold oligotrophic waters, lakes, rivers, streams. Oligotrophic to eutrophic waters, lakes.
Elevation 0–2800 m. (0–9200 ft.) 0–3300 m. (0–10800 ft.)
Distribution
from FNA
AZ; CA; ID; MT; OR; UT; WA; WY; BC; NB; PE; s Mexico; South America
[WildflowerSearch map]
[BONAP county map]
from FNA
AK; AZ; CA; CO; CT; DE; IA; ID; IL; IN; KS; MA; MD; ME; MI; MN; MO; MT; ND; NE; NH; NJ; NM; NV; NY; OH; OR; PA; RI; SD; TX; UT; VT; WA; WI; WY; AB; BC; MB; NB; NL; NS; NT; NU; ON; PE; QC; SK; YT; Greenland; Eurasia
[WildflowerSearch map]
[BONAP county map]
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.)

Myriophyllum exalbescens (M. sibiricum) was considered to be a North American endemic until the discovery of European specimens (S. G. Aiken and J. McNeill 1980). Since the taxonomic name of Russian material pre-dated that for North American specimens, all material of M. exalbescens was synonymized under the name M. sibiricum (A. Ceska and O. Ceska 1986; Aiken and A. Cronquist 1988). Myriophyllum sibiricum is widely recognized as circumpolar with an affinity for colder climates and is rarely found south of the 0°C January isotherm (Aiken 1981). Myriophyllum sibiricum is distinctive when growing with low leaf segment numbers. Hybridization with M. spicatum and subsequent introgression has apparently blurred the boundaries between these two taxa to the point that some specimens are not assignable to either species without molecular analysis (see 8. M. spicatum). There is concern that M. sibiricum is being rapidly outcompeted in lakes by either M. spicatum or its hybrid (M. L. Moody and D. H. Les 2007b; A. P. Sturtevant et al. 2009; E. A. LaRue et al. 2013). The dark green cylindric turions in M. sibiricum, which have reduced and thickened storage leaves, are useful for identification. These reduced leaves are often blackened and visible at the base of new shoots in the next growing season, which can aid in the identification of vegetative material.

(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
M. alterniflorum, M. aquaticum, M. farwellii, M. heterophyllum, M. hippuroides, M. humile, M. laxum, M. pinnatum, M. sibiricum, M. spicatum, M. tenellum, M. ussuriense, M. verticillatum
M. alterniflorum, M. aquaticum, M. farwellii, M. heterophyllum, M. hippuroides, M. humile, M. laxum, M. pinnatum, M. quitense, M. spicatum, M. tenellum, M. ussuriense, M. verticillatum
Synonyms M. elatinoides M. exalbescens, M. magdalenense, M. spicatum var. capillaceum, M. spicatum subsp. exalbescens, M. spicatum var. exalbescens, M. spicatum var. muricatum
Name authority Kunth in A. von Humboldt et al.: Nov. Gen. Sp. Pl. 6(fol.): 71; 6(qto.): 89. (1823) Komarov: Repert. Spec. Nov. Regni Veg. 13: 168. (1914)
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