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Eurasian water-milfoil, myriophylle en épi, spike water milfoil, water milfoil

water-milfoil family

Habit Herbs monoecious, aquatic, often forming dense stands. Herbs, perennial [annual], or shrubs, usually monoecious, rarely dioecious, usually aquatic to semiaquatic, sometimes terrestrial, unarmed, ± clonal.
Roots

taproots or fibrous, and then often with adventitious nodal roots;

rhizomes sometimes present [stolons in some Haloragis].

Stems

often much-branched distally, to 6 m. Turions absent.

erect, ascending, decumbent, or prostrate, cylindric to 4-ribbed, glabrous or scabrous to pubescent, hairs uniseriate and multiseriate, glands present or absent.

Turions

present or absent, lateral and/or terminal.

Leaves

in whorls of (3 or)4(or 5), heteromorphic;

petiole 0–0.4 mm; submersed leaves pectinate, obovate in outline, (14–)18–32(–36) × 10–20(–30) mm, segments (20–)24–36(–42), linear-filiform, longest segment 2–20(–26) mm, usually parallel and all in 1 plane, forming angles less than 45° with central axis; emersed leaves pectinate to pinnatifid proximally, with abrupt transition to obovate or 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.

opposite, alternate, or subverticillate to whorled, simple, often heteromorphic in Myriophyllum and Proserpinaca;

stipules absent;

sessile or petiolate;

blade lobed, unlobed, or pinnatifid to pectinate, margins entire or serrate, surfaces glabrous or scabrous.

Inflorescences

to 15 cm;

flowers proximally pistillate, medially bisexual, distally staminate;

bracteoles cream to stramineous to purple, with distinct reddish or brown margins, usually ovate to depressed-ovate or obovate, sometimes elliptic to triangular or rhombic, 0.5–0.9 × 0.4–0.7 mm, margins entire or serrate, sometimes with distal, irregular, membranous fringe.

terminal or lateral in axils of bracts or leaves, determinate or indeterminate, dichasia (Haloragis and Proserpinaca), or simple racemes (Myriophyllum);

bracts and bracteoles present.

Flowers

bisexual or unisexual, staminate and pistillate usually on same plant, sessile or pedicellate (sometimes sessile in pistillate flowers of Myriophyllum);

perianth and androecium epigynous;

hypanthium subglobose;

sepals persistent, (3 or)4, sometimes rudimentary (Myriophyllum), petals often caducous, sometimes persistent, (3 or)4, or 0 or rudimentary (Proserpinaca), keeled, cucullate, often distally cupulate;

stamens 3–8 (1 or 2 times as many as sepals);

anthers basifixed, dehiscing longitudinally;

pistil 1, 3- or 4-carpellate;

ovary 1, inferior, 1–4-locular;

placentation axile;

styles 1 per locule;

stigmas 1 per locule, clavate, capitate, fimbriate;

ovules 1(or 2, in Haloragis and Proserpinaca), anatropous, bitegmic, crassinucellate.

Staminate flowers

sepals cream to stramineous, triangular, 0.3–0.4 × 0.2–0.3 mm;

petals caducous, cream to red or dark purple, oblong to elliptic or obovate, 1.5–2.5(–3) × 0.8–1 mm;

stamens 8, filaments to 1.2 mm, anthers greenish cream to yellow or purple, 1–2.2 × 0.4–0.8 mm.

Pistillate flowers

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, 0.6–0.8 × 0.3–0.4 mm;

pistils 0.9–1.2 mm, stigmas white to red to ± purple, 0.2–0.7 mm.

Fruit(s)

globose, 4-lobed.

a nutlet, indehiscent, or schizocarp, splitting into (2–)4 mericarps;

exocarp glabrous, scabrous, rugose, tuberculate, or papillate, sometimes with ribs, ridges, or wings.

Seeds

1 per locule;

embryo straight, cylindric;

endosperm ± copious and fleshy.

Mericarps

olive-green to brown, cylindric to narrowly ovoid, 1.5–2.2 × 0.8–1.3 mm, transversely widely obovate, abaxial surface broadly rounded, sparsely and irregularly tuberculate, margins smooth to tuberculate, sometimes with 2 shallow, longitudinal ridges, wings and ribs absent.

2n

= 42.

Myriophyllum spicatum

Haloragaceae

Phenology Flowering and fruiting Apr–Oct.
Habitat Oligotrophic to eutrophic waters, lakes, ponds, canals, streams.
Elevation 0–1500 m. (0–4900 ft.)
Distribution
from FNA
AL; AR; AZ; CA; CO; CT; DC; DE; FL; GA; IA; ID; IL; IN; KS; KY; LA; MA; MD; MI; MN; MO; MS; MT; NC; ND; NE; NH; NJ; NV; NY; OH; OK; OR; PA; RI; SC; TN; TX; UT; VA; VT; WA; WI; WV; BC; NB; ON; QC; Eurasia; n Africa [Introduced in North America]
[WildflowerSearch map]
[BONAP county map]
North America; Mexico; Central America; South America; West Indies; Bermuda; Eurasia; Africa; Indian Ocean Islands; Pacific Islands; Australia
[BONAP county map]
Discussion

Myriophyllum spicatum is considered one of the worst nuisance aquatic weeds in North America. Identification of this species is critical for management of lakes. Until the early 1900s, the widely accepted view was that M. spicatum was native to North America and was conspecific with European M. spicatum. M. L. Fernald (1919c) described M. exalbescens to distinguish all North American specimens from European M. spicatum, with the former name subsequently being changed to M. sibiricum due to nomenclatural precedence (S. G. Aiken and A. Cronquist 1988). The first to recognize the presence of both species in North America was apparently C. F. Reed (1970b). E. Hultén (1941–1950), B. C. Patten (1954), and S. A. Nichols (1975) proposed alternatively that M. spicatum and the native M. sibiricum form a continuum of variation, suggesting the two taxa may simply represent varieties or subspecies of a highly variable cosmopolitan species. Based on a study of herbarium collections, R. Couch and E. Nelson (1985, 1992) believed that M. spicatum was introduced from Europe in the 1940s and subsequently spread throughout the United States and Canada. A recent biogeographic study of cpDNA haplotypes indicates this species was introduced to North America from China and Korea (M. L. Moody et al. 2016).

Based upon examination of specimens for this treatment, and as pointed out by A. E. Orchard (1981), most of the characters initially proposed by M. L. Fernald (1919c) and expanded upon by S. G. Aiken (1981) that are thought to be reliable for distinguishing the two species, such as size and shape of floral bracts and bracteoles, anther length, swollen base of inflorescence, color of the stem in dried material, extent of branching, and differences in mericarps, break down when a wide range of North American herbarium material is examined. One of the few useful vegetative characters to distinguish these species in the northern regions of North America is that M. sibiricum often produces turions in the latter part of the growing season, whereas M. spicatum does not (E. Hultén 1947). The most commonly used vegetative character to distinguish the two species is the number of leaf segments in submersed leaves (Fernald). When attempting to distinguish plants of the latter two species, this is a reliable character, but only when specimens have low (6–18) or high (24–42) segment numbers; plants often have submersed leaves with intermediate segment numbers.

Molecular studies have shown that the overlap seen in morphological characters, such as leaf segment number, between Myriophyllum sibiricum and M. spicatum may be the result of frequent and widespread hybridization (M. L. Moody and D. H. Les 2002, 2007b; A. P. Sturtevant et al. 2009). Hybrids between these two species can have leaf segment numbers from 16–28 (Moody and Les 2007b), which overlaps with leaf segment numbers for both M. sibiricum (6–18) and M. spicatum (24–36). A reliable method to distinguish these taxa when there is overlap in this character state is DNA fingerprinting (Moody and Les 2002).

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Genera 10, species ca. 120 (3 genera, 17 species in the flora).

Morphologically, Haloragaceae are defined by the following floral characters: an epigynous ovary, usually 3- or 4-merous floral organization (always 3-merous in Proserpinaca), sometimes 2-merous, cucullate petals, and fruit a nutlet or schizocarp with 1 or 2 ovules per locule. In the aquatic members of the family, reliance on vegetative characters that are highly plastic and have evolved independently by convergent evolution has proven to be of limited usefulness for the delimitation of taxa (M. L. Moody and D. H. Les 2007).

J. Hutchinson (1959) suggested that Haloragaceae is closely allied to Onagraceae based on embryology, pollen morphology, and floral vasculature. A. Cronquist (1968) and A. L. Takhtajan (1969) believed Haloragaceae to be more closely allied to Podostemaceae. The work of A. E. Orchard (1975, 1985) has been important in circumscribing the family.

Molecular phylogenetic studies have placed Haloragaceae within the core eudicot order Saxifragales (D. R. Morgan and D. E. Soltis 1993; Soltis et al. 1997b). Gunnera, which had long been included within the family, has been moved to the monogeneric family Gunneraceae in Gunnerales (Angiosperm Phylogeny Group 2009).

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Key
1. Flowers unisexual or bisexual, proximal pistillate, distal staminate, often with intermediate transitional zone of bisexual flowers; fruit a schizocarp, splitting into (2–)4 mericarps; plants aquatic or semiaquatic.
Myriophyllum
1. Flowers bisexual; fruit a nutlet, indehiscent; plants aquatic, semiaquatic, or terrestrial.
→ 2
2. Flowers 4-merous; plants shrubs or herbs, terrestrial.
Haloragis
2. Flowers 3-merous; plants herbs, aquatic or semiaquatic.
Proserpinaca
Source FNA vol. 10. FNA vol. 10. Authors: Robin W. Scribailo, Mitchell S. Alix.
Parent taxa 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. tenellum, M. ussuriense, M. verticillatum
Subordinate taxa
Haloragis, Myriophyllum, Proserpinaca
Name authority Linnaeus: Sp. Pl. 2: 992. (1753) R. Brown
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