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Russian water-milfoil, terrestrial water milfoil, Ussurian milfoil, Ussurian water-milfoil

low water-milfoil, myriophylle menu, western water-milfoil

Habit Herbs usually dioecious, rarelymonoecious, aquatic or semiaquatic, usually not forming dense stands. Herbs monoecious, aquatic or semiaquatic, usually not forming dense stands.
Stems

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.

often branched, to 1 m. Turions absent.

Leaves

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.

usually alternate or opposite, rarely in whorls of 3(or 4), heteromorphic;

petiole to 4 mm; submersed leaves pectinate, ovate to elliptic in outline, (5.5–)10–27(–30) × (4.4–)6–22(–33) mm, segments (2–)4–13(–14), linear-filiform, longest segment (3–)8–17(–22.5) mm; emersed leaves usually pectinate to pinnatifid proximally, linear to spatulate or lobed distally, 5–9(–12.5) × 0.3–3(–6) mm, segments (0–)4–6(–9).

Inflorescences

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.

to 35 cm, sometimes submersed with flowers in axils of unmodified, pectinate leaves;

flowers proximally pistillate, distally staminate;

bracteoles cream, oblong to elliptic to ovate or triangular, 0.3–0.7 × 0.1–0.4 mm, margins entire or irregularly lobed, apex often aristate.

Staminate flowers

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.

sepals cream to stramineous, triangular, 0.1–0.2 × 0.1–0.2 mm;

petals caducous, purple, elliptic to obovate, 0.6–1.5 × 0.3–0.7 mm;

stamens 4, filaments to 0.9 mm, anthers 0.3–0.8 × 0.1–0.3 mm.

Pistillate flowers

sepals and petals rudimentary or absent;

pistils to 0.7 mm, stigmas white, to 0.3 mm.

sepals cream to stramineous, triangular, 0.1–0.2 × 0.1 mm;

petals caducous, purple, elliptic to obovate, 0.3–0.5 × 0.2–0.3 mm;

pistils 0.7–0.9 mm, stigmas red to ± purple, to 0.2 mm.

Fruits

subglobose, 4-lobed.

cylindric, deeply 4-lobed.

Mericarps

brown, obovate, 0.8 × 0.6 mm, abaxial surface rounded, minutely tuberculate, wings and ribs absent.

tan to red-brown or purple, cylindric to narrowly ovoid, (0.6–)0.8–1.2 × 0.4–0.6 mm, transversely elliptic to ovate, abaxial surface rounded, sparsely to densely tuberculate, tubercles relatively small, shallow, wings and ridges absent.

2n

= [14] 21.

Myriophyllum ussuriense

Myriophyllum humile

Phenology Flowering and fruiting Jul–Nov. Flowering and fruiting Jun–Oct.
Habitat Streams, rivers, muddy shorelines of ponds and lakes, intertidal wetlands. Oligotrophic waters, lakes, ponds, streams.
Elevation 0–600 m. (0–2000 ft.) 0–700 m. (0–2300 ft.)
Distribution
from FNA
OR; WA; BC; Eurasia
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from FNA
CT; DE; MA; MD; ME; NH; NJ; NY; PA; RI; VA; VT; NB; NS; QC
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Discussion

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.)

Myriophyllum humile has a diminutive semiterrestrial growth form, referred to as var. limosum by T. Morong (1891), that has alternate and, typically, spatulate floral bracts that can be confused with the emergent form of M. pinnatum. In vegetative form, the leaves of M. pinnatum tend to be pectinate with a greater number of longer segments than those of M. humile, which are often linear, spatulate, or 4–6-lobed. When fruits are present, the two can be distinguished by the presence of winged ridges on the mericarps in M. pinnatum, which are absent in M. humile. Submersed forms of M. humile can be confused with M. farwellii because of the delicate nature of their leaves. M. humile has leaves mostly alternate and opposite; leaves in M. farwellii tend to be whorled or, sometimes, subverticillate, giving these plants a bushy appearance. Myriophyllum humile can be also confused with M. laxum (see 10. M. laxum discussion).

All specimens examined from Minnesota labeled Myriophyllum humile have been misidentified and are other species of the genus. Only one sterile herbarium specimen labeled as M. humile from Wisconsin has been seen, but its identity could not be confirmed.

(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. quitense, M. sibiricum, M. spicatum, M. tenellum, M. verticillatum
M. alterniflorum, M. aquaticum, M. farwellii, M. heterophyllum, M. hippuroides, M. laxum, M. pinnatum, M. quitense, M. sibiricum, M. spicatum, M. tenellum, M. ussuriense, M. verticillatum
Synonyms M. verticillatum var. ussuriense Burshia humilis, M. ambiguum var. limosum, M. procumbens
Name authority (Regel) Maximovicz: Bull. Acad. Imp. Sci. Saint-Pétersbourg 19: 182. (1873) (Rafinesque) Morong: Bull. Torrey Bot. Club 18: 242. (1891)
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