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glasswort, pickleweed, saltwort, samphire

Habit Herbs, annual, fleshy, glabrous.
Stems

prostrate to erect, simple to many-branched, apparently jointed and fleshy when young, becoming not jointed and somewhat woody with age.

Leaves

opposite, connate basally, sessile, decurrent portions forming fleshy segments enclosing stem, fleshy;

blade reduced to fleshy scales, margins entire, narrow, scarious.

Inflorescences

spikes, terminal on each stem, apparently jointed, each joint (fertile segment) consisting of 2 axillary, opposite, usually 3-flowered cymes embedded in and adherent to fleshy tissue of distal internode;

flowers in each cyme arranged in triangle, the 2 lateral flowers meeting beneath central flower, flowers separated by persistent flaps of internodal tissue.

Flowers

usually bisexual, ± radially symmetric;

perianth segments persistent in fruit, usually 3, connate except for extreme tips, fleshy;

stamens (0–)1–2;

styles 2.

Fruits

utriclelike;

pericarp membranous.

Seeds

vertical, ellipsoid;

seed coat yellowish brown, thin, membranous, hairy;

perisperm absent.

x

= 9.

Salicornia

Distribution
from USDA
Northern Hemisphere; s Africa
[BONAP county map]
Discussion

Species ca. 10 (4 in the flora).

Salicornia is occasionally utilized as a vegetable in Europe, especially the tetraploid species. The seeds are rich in oils and experimental trials have been undertaken in the southwestern United States to harvest tetraploid species, especially S. bigelovii, on a large scale as a commercial source of vegetable oils.

Because of the succulence of the plants and the highly reduced morphology, it has been difficult to develop a satisfactory taxonomy of the genus. Dried specimens often cannot be determined with certainty, and are of little use in taxonomic studies owing to the loss of characteristics on drying. Salicornia is also difficult to cultivate satisfactorily because the plants appear to require a limited amount of salt and, the tetraploids in particular, occasional submersion in water, although they do not grow well in permanently waterlogged soils.

R. L. Jefferies and L. D. Gottlieb (1982) and S. L. Wolff and R. L. Jefferies (1987, 1987b), using isozyme data, have shown that the diploid taxa are largely homozygous inbreeding lines. There is for the most part good correlation between morphological and isozyme data, but it must be emphasized that the geographical coverage and the number of populations studied are limited.

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

Key
1. Leaf and bract apices acute and sharply mucronate; bracts almost obscuring cymes
S. bigelovii
1. Leaf and bract apices obtuse to subacute, not mucronate; bracts covering only bases of cymes
→ 2
2. Fertile segments ± cylindric; anthers all exserted, dehiscing after exsertion
S. depressa
2. Fertile segments widest distally; anthers commonly not exserted, mostly dehiscing within flower
→ 3
3. Anthers (0.1-)0.2-0.3 mm; coastal
S. maritima
3. Anthers (0.2-)0.3-0.4 mm; inland
S. rubra
Source FNA vol. 4. Author: Peter W. Ball.
Parent taxa Chenopodiaceae
Subordinate taxa
S. bigelovii, S. depressa, S. maritima, S. rubra
Name authority Linnaeus: Sp. Pl. 1: 3. (1753): Gen. Pl. ed. 5, 4. (1754)
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