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common eel-grass, eel-grass, grass wrack, seawrack, zostère marine

eel-grass, zostère

Habit Herbs, perennial. Herbs, perennial or rarely annual, rooted in substrate.
Roots

5–20, nodal.

Rhizomes

2–6 mm thick;

roots 5–20 at each node.

Leaves

sheath tubular, rupturing with age, 5–20 cm, membranous flaps absent;

blade to 110 cm × 2–12 mm, apex round-obtuse or slightly mucronate;

veins 5–11.

sheath tubular or open, persisting longer than blade, often rupturing with age but not remaining as bundles of woolly fibers;

blade entire or slightly denticulate distally;

veins 3–11.

Inflorescences

peduncles with adnate portion 15–100 mm, free portion 2–3 cm;

spathes 10 or more, sheath 4–8 cm × 2–5 mm;

blade 5–20 cm;

spadix linear; staminate flowers 1–20; pistillate flowers 1–20, apex acute or mucronate.

peduncle partially adnate to stem;

spadix lanceolate, enclosed permanently within spathe sheath; staminate and pistillate flowers alternating on same spadix; pistillate spadix without rudimentary staminate flowers.

Staminate flowers

bracts absent or rarely 1 subtending most proximal flower;

pollen sacs 4–5 × 1 mm.

often subtended by bract.

Pistillate flowers

ovary 2–3 mm, style 1–3 mm.

without subtending bract, pistil elliptic.

Fruits

ellipsoid to ovoid, 2–5 mm, often beaked.

achenelike, ovoid to ellipsoid.

Generative

shoots terminal, repeatedly branched, each branch with 1–5 spathes.

shoot lateral or terminal.

Zostera marina

Zostera

Phenology Flowering late spring–summer.
Habitat Intertidal to sublittoral of marine waters
Elevation -10–0 m (-0–0 ft)
Distribution
from FNA
AK; CA; CT; DE; MA; MD; ME; NC; NH; NY; OR; RI; VA; WA; BC; NB; NF; NS; NU; ON; PE; QC; YT; Mexico (Baja California, Sinaloa, Sonora); Eurasia
[WildflowerSearch map]
[BONAP county map]
from USDA
Temperate waters worldwide
[BONAP county map]
Discussion

Zostera marina is adapted to the cold waters of the North Atlantic and North Pacific. It extends southward to North Carolina in the Atlantic and Baja California in the Pacific. At the southern limits of its range, active growth mostly is in the cooler months of autumn and spring, with flowering and fruiting mostly in the spring and the plants dying in the hotter summer months, the vegetation becoming dislodged from the substrate and floating to the water surface. The fruits apparently remain in the floating vegetation for a period of time, eventually falling from the shoots to the substrate. Movement in dislodged vegetative material is the only adaptation the fruits have for dispersal (C. den Hartog 1970).

The species is found mostly in the sublittoral region, only rarely being exposed at low tide. It occurs in more or less sheltered areas on soft mud or firm sand. Plants of sandy substrates had narrower leaves than plants growing on muddy substrates (C. H. Ostenfeld 1905). Fruits fall from the floating vegetation to the substrate and settle on the substrate ripple marks, which run more or less perpendicular to the direction of current. Seedling establishment is parallel with the ripple marks, forming vegetated ridges separated by depressions, which gradually fill with sediments, and the plants then grow laterally into them, forming a meadow (C. den Hartog 1970). The vegetation lowers the velocity of current flow, causing some suspended particles to settle out and accumulate around the base of the plants, slowly building the substrate. As more particles accumulate, the substrate gets deeper over the rhizomes, since the rhizomes grow horizontally, not vertically. Eventually, the rhizomes are too deep, and the plants begin to die back, a phenomenon followed by erosion.

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

Zostera, especially Z. marina, is very possibly the most important taxon of marine angiosperms in the Northern Hemisphere. Much has been written about the biology and economic importance of Z. marina, and the literature was summarized by C. den Hartog (1970). The species functions in sediment deposition, substrate stabilization, as substrate for epiphytic algae and micro-invertebrates, and as nursery grounds for many species of economically important marine vertebrates and macro-invertebrates. In addition to those functions, the species once was the principal material for the Dutch dikes, and it has been utilized as packing material and as stuffing for mattresses and cushions. Finally, the species has been used for food and recreation by the Seri tribe of Native Americans (R. Felger and M. B. Moser 1973).

During the 1930s, Zostera marina of North America began to develop large brown spots on the leaves and rhizomes. Slowly the plants of a population died, the dieback eventually spreading throughout the North Atlantic, until there was very little eel-grass remaining there. This slow dieback of eel-grass became known as "wasting disease." Biologists began studying the disease and eventually determined the causative agent to be Labyrinthula zosterae, a slime mold. That dieback resulted in huge decreases in the population sizes of most fauna that depended on Zostera. Slowly, eel-grass returned to most areas that it had occupied prior to the disease.

Species 12 (2 in the flora).

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

Key
1. Leaf sheath tubular, without membranous flaps, rupturing with age; bract absent or rarely 1 subtending lowermost staminate flower.
Z. marina
1. Leaf sheath open, with 2 membranous flaps, persisting without rupturing; bract subtending each staminate flower.
Z. japonica
Source FNA vol. 22. FNA vol. 22.
Parent taxa Zosteraceae > Zostera Zosteraceae
Sibling taxa
Z. japonica
Subordinate taxa
Z. japonica, Z. marina
Synonyms Z. marina var. stenophylla
Name authority Linnaeus: Sp. Pl. 2: 968. (1753) Linnaeus: Sp. Pl. 2: 968. 1753; Gen. Pl. ed. 5; 415, (1754)
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