A handbook of systematic botany

Order 10. Sphæropleaceæ. The thallus consists of free, unbranched filaments, with very elongated multinuclear cells. The vegetative cells form no zoospores. Sexual reproduction by oogamous fertilisation (see page 13, Fig. 10 B). The oospore has a thick wall (Fig. 10 D) studded with warts, and assumes a colour resembling red lead. It germinates only in the following spring, and produces 1–8 zoospores, each with 2 cilia (Fig. 10 E), which grow into new filaments. Only one species, Sphæroplea annulina, is known.

Family 3. Siphoneæ.

The thallus has apical growth, and in the vegetative condition consists generally of one single (in the Valoniaceæ most frequently of more) multinuclear cell, which may be much branched, and whose separate parts in the higher forms (e.g. Bryopsis, Fig. 57; Caulerpa, Fig. 59, etc.) may be differentiated to perform the various physiological functions (as root, stem and leaf). Vegetative multiplication by detached portions of the thallus (gemmæ); asexual reproduction by zoospores, akinetes, or aplanospores. Sexual reproduction by gamete-conjugation, rarely by oogamous fertilisation. The zygote or oospore germinates as a rule without any resting-stage.

Most of the Siphoneæ occur in salt water or on damp soil. Many (e.g. Dasycladaceæ) are very much incrusted with lime, and occur, in the fossilized condition, in the deposits from the Cretaceous period to the present time. The Siphoneæ are connected by their lowest forms (Botrydiaceæ or Valonia) with the Protococcaceæ, but show also, through the Valoniaceæ, points of relationship to the Cladophoraceæ.

Order 1. Botrydiaceæ. The thallus in the vegetative condition is unicellular, club-shaped, with a small single (Codiolum) or repeatedly dichotomously branched system of colourless rhizoids (Botrydium, Fig. 56 a), by which it is attached to objects immersed in salt water (Codiolum) or to damp clay soil (Botrydium). Asexual reproduction by zoospores with one (Botrydium) or two cilia, and by aplanospores. The sexual reproduction is only known in Botrydium, and takes place in the following manner: in the part of the thallus which is above ground and in an active vegetative condition, several round cells (Fig. 56 c) are formed, which may be green or red according as they grow under water, or exposed to the strong light of the sun. These cells must be considered as “gametangia” as they produce many gametes (d) provided with two cilia. The zygote (h, i) formed by the conjugation (e, f, g) may either germinate immediately, or become a thick-walled resting-cell of an irregular, angular form.

Order 4. Vaucheriaceæ. The thallus consists, in the vegetative condition, of a single irregularly or dichotomously branched cell, without differentiation into stem or leaf; root-like organs of attachment may however occur. Asexual reproduction by zoospores, which are formed singly in the extremity of a branch cut off by a transverse wall. They contain many nuclei, and bear small cilia situated in pairs, which give the appearance of a fine “pile” covering the whole or a great part of the surface. Akinetes, aplanospores, and phytoamœbæ (naked masses of protoplasm, without cilia, which creep like an amœba on a substratum) may occur under certain conditions.

The sexual reproductive organs are formed on short lateral branches, and are separated from the vegetative cell (Fig. 58 A) by cell-walls. Numerous spermatozoids, each with two cilia, are developed in the coiled antheridium (A, b). The oogonium is a thick, egg-shaped, often oblique cell, with its protoplasm rounded into an oosphere, which has a hyaline “receptive-spot” (A, a) immediately beneath the aperture formed in the wall of the oogonium. A slimy mass, which serves to receive the spermatozoids, is formed in some species in this aperture. The spermatozoids when liberated swim towards and enter the oosphere, which then immediately surrounds itself with a thick cell-wall. The mature oospore (B) contains a large quantity of oil. At germination the outer cell-wall bursts and a new plant is formed. There is only one genus, Vaucheria, with species living in salt as well as in fresh water and on damp soil.

Order 6. Caulerpaceæ. The thallus has distinct differentiation into root, stem and leaf-like members (Fig. 59); it is unicellular. Within the cell, strong, branched threads of cellulose extend from one side to the other serving as stays to support the thallus. Reproduction takes place by detached portions of the thallus; no other modes of reproduction are known. This order may most approximately be classed with the Bryopsidaceæ. The genus Caulerpa consists of more than seventy species which inhabit the tropical seas.

Order 7. Codiaceæ. The thallus has various forms, but without distinct differentiation in stem- or leaf-structures, sometimes (e.g. Halimeda) it is very much incrusted with lime. In the early stages it is unicellular (later, often multicellular), very much branched, with the branches, at any rate partly, so united or grown in amongst one another (Fig. 60) that an apparently parenchymatous cellular body is formed. Akinetes or aplanospores are wanting; zoospores (or gametes?) may be developed in some species, however, in special swollen sporangia. Fertilisation similar to that in Bryopsis occurs perhaps in Codium. They are all salt water forms.

Order 9. Dasycladaceæ. The thallus consists of an axile longitudinal cell, destitute of transverse walls, attached at the base by root-like organs of attachment, and producing acropetally whorls of united, single or branched, leaf-like structures with limited growth. Asexual reproduction is wanting. Sexual reproduction by conjugation of gametes which arise in separate, fertile leaves, either directly or from aplanospores, which develope into gametangia. The principal genera are: Acetabularia, Dasycladus, Neomeris, Cymopolia. All marine.

The curiously shaped Acetabularia mediterranea grows gregariously on limestone rocks, and shells of mussels in the Mediterranean; it resembles a minute umbrella with a small stem, sometimes as much as nine centimetres in height, and a shade which may be more than one centimetre in diameter. The cell-membrane is thick, and incrusted with carbonate and oxalate of lime. Only the lower, root-like part of the thallus, which penetrates the calcareous substratum survives the winter, and may grow up into a new plant. The sterile leaves, which drop off early, are dichotomously branched and formed of cylindrical cells separated from each other by cross-walls, but they are not grown together. The shade is formed by a circle of 70–100 club-shaped rays (fertile leaves) grown together, in each ray 40–80 aplanospores are formed, which become liberated at the breaking of the shade, and later on are changed to gametangia (compare Botrydium) which open by a lid and allow a large number of egg-shaped gametes with two cilia to escape. Gametes from various gametangia conjugate with one another; the product of the conjugation swarms about for some time, rounds off, and then surrounds itself with a cell-wall. The zygote germinates after a period of rest and then produces a sexual plant. The aplanospores (gametangia) thus represent the sexual generation.

Class 7. Characeæ.

The thallus has a stem with nodes and internodes; and whorls of leaves, on which may be developed the antheridia and oogonia, are borne at the nodes. Vegetative reproduction by bulbils and accessory shoots. Zoospores are wanting. The antheridia are spherical, and contain a number of filaments in which the spirally coiled spermatozoids, each with two cilia, are formed. The oogonium is situated terminally, and is at first naked, but becomes later on surrounded by an investment, and forms after fertilisation the so-called “fruit.” The oospore, after a period of rest, germinates by producing a “proembryo,” from which the young sexual plant arises as a lateral branch. The Characeæ are distinguished by the structure of their vegetative system as well as by the spirally-coiled spermatozoids, and stand as an isolated group among the Thallophytes, of which, however, the Siphoneæ appear to be their nearest relations. They were formerly, but wrongly, placed near the Mosses. The class contains only one order, the Characeæ.

Order 1. Characeæ. Algæ with a peculiar odour, often incrusted with lime, and of a brittle nature. They generally grow gregariously in large masses at the bottom of fresh and brackish water, and are from a few inches to more than a foot in height. The stem has long internodes which in Nitella are formed of one cylindrical cell; in Chara of a similar cell, but closely surrounded by a cortical layer of smaller ones. The protoplasm in contact with the cell-wall exhibits in a well-marked degree the movement of rotation (cyclosis), carrying the chlorophyll corpuscles along with it. The internodes are separated from each other by a layer of small cells (nodal cells) from which the leaves are produced. The leaves are borne in whorls of from 5–12 which regularly alternate with one another as in the higher verticillate plants; a branch is borne in the axil of the first formed leaf of each whorl (Fig. 61 A, n).

The leaves are constructed in the same manner as the stem; they are divided into a series of joints, but have only a limited power of growth; their terminal cell, too, is not enclosed by a cortex. Leaflets are borne at their nodes. The growth of the stem is unlimited, and proceeds by means of an apical cell (Fig. 62 s). The apical cell divides into a segment-cell and a new apical cell. The segment-cell then divides by a transverse wall into two cells, one lying above the other; the lower one, without any further division, becomes one of the long, cylindrical, internodal cells (Fig. 62 in), and the upper one (Fig. 62 n) divides by vertical walls to form the nodal cells. The cortical cells (Fig. 62 r) which surround the long internodal cells of Chara, are derived from the divisions of the nodal cells; the cells covering the upper portion of an internodal cell being derived from the node immediately above it, and those in the lower part of the internode from the node below it.

The organs of reproduction are very conspicuous by their colour and form. They are always situated on the leaves, the plants being very frequently monœcious. The antheridia (Fig. 61 B, a) are modified leaflets or the terminal cell of a leaf; they are spherical and become red when mature. Their wall consists of 8 “shields,” i.e. of plate-like cells, 4 of which cover the upper half, and are triangular; the 4 round the lower half, to which the stalk of the antheridia is attached, being quadrilateral, with sides of unequal length. The shields (Fig. 61 C) have dentated edges, with the teeth fitting into one another, and their faces ornamented with ridges. From the centre of the internal face of each shield (C) a cylindrical cell, the manubrium, projects nearly as far as the centre of the antheridium; at the inner end of each of the manubria a spherical cell, the capitulum, is situated. Each capitulum bears six secondary capitula, from each of which four long coiled filaments (C, D) project into the cavity of the antheridium. These filaments are divided by transverse walls into from 100–200 discoid cells, in each of which a biciliated, coiled spermatozoid is developed (D, E) from the nucleus. The spermatozoids escape from their mother-cell and are set free by the shields separating from one other.

The female organ of reproduction (Fig. 61 B, 63) is a small modified shoot, whose apical cell functions as an oogonium, its protoplasm forming the oosphere, which has a colourless receptive-spot at the summit (Fig. 63 u). The oogonium is situated on a nodal cell, from which 5 cells grow out in a circle and coil round the oogonium, covering it with a close investment. These cells divide once or twice at the top, so that 5 or 10 small cells are cut off, which project above the oogonium and form the so-called “crown” (Fig. 63 k). The crown either drops off at fertilisation, or its cells separate to form a central canal for the passage of the spermatozoids. The wall of the oosphere[9] above the receptive spot becomes mucilaginous, and allows the spermatozoid to fuse with the oosphere. The oospore, on germination (Fig. 64 sp), becomes a small filamentous plant of limited growth (Fig. 64 i, d, q, pl)—the proembryo—and from this, as a lateral outgrowth, the sexual generation is produced.

The order is divided into two sub-orders:—

A. Nitelleæ. The crown consists of 10 cells; cortex absent: Nitella, Tolypella.

B. Chareæ. The crown consists of 5 cells; cortex present: Tolypellopsis, Lamprothamnus, Lychnothamnus, Chara.

Chara crinita is parthenogenetic; in large districts of Europe only female plants are found, yet oospheres are formed capable of germination.

About 40 species of fossilized Chara, determined by their carpogonia, are known in the geological formations from the Trias up to the present day.

Class 8. Phæophyceæ (Olive-Brown Seaweeds).

The Phæophyceæ are Algæ, with chromatophores in which the chlorophyll is masked by a brown colour (phycophæin). The product of assimilation is a carbohydrate (fucosan), never true starch. In the highest forms (Fucaceæ), the thallus presents differentiation into stem, leaf, and root-like structures. The asexual reproduction takes place by means of zoospores. The sexual reproduction is effected by the coalescence of motile gametes, or by oogamous fertilisation. The swarm-cells are monosymmetric, each moved by two cilia which are true protoplasmic structures, and generally attached laterally (Fig. 65). The Phæophyceæ are almost entirely saltwater forms; a few species of Lithoderma live in fresh water.

The class is divided into two families:—

1. Phæosporeæ: 1 Sub-Family, Zoogonicæ; 2 Sub-Family, Acinetæ.

2. Cyclosporeæ: Fucaceæ.

Family 1. Phæosporeæ.

The family consists of multicellular plants, whose cells are firmly united together to form a thallus; this, in the simplest cases, may be a branched filament of cells (Ectocarpus), or, in the highest, may resemble a stem with leaves (Laminariaceæ), while all transitional forms may be found between these two. The thallus grows by intercalary divisions (e.g. Ectocarpus), or by an apical cell (e.g. Sphacelaria); pseudo-parenchymatous tissue may sometimes be formed by cells, which were originally distinct, becoming united together. The size of the thallus varies; in some species it is quite small—almost microscopical,—while in the largest it is many metres in length.

The vegetative cells in the lower forms are nearly uniform, but in those which are more highly developed (Laminariaceæ and Fucaceæ), they are sometimes so highly differentiated that mechanical, assimilating, storing and conducting systems may be found; the last named systems are formed of long cells with perforated, transverse walls, which bear a strong resemblance to the sieve-tubes in the higher plants.

The colouring matter in the living cells (“phæophyl”) contains chlorophyll; but this is concealed by a brown (“phycophæin”), and a yellow (“phycoxanthin”) colouring material, and hence all these Algæ are a lighter or darker yellow-brown. Starch is not formed. Asexual reproduction takes place, (1) by zoospores which arise in unilocular zoosporangia, and are monosymmetric, with two cilia attached laterally at the base of the colourless anterior end (Fig. 65), the longer one being directed forwards and the shorter backwards; or (2) by aplanospores (?).

Sexual reproduction has only been discovered in a few cases, and takes place by means of gametes (oogamous fertilisation perhaps occurs in the Tilopteridæ). The gametes have the same structure as the zoospores, and arise in multilocular gametangia; these, like the zoosporangia, are outgrowths from the external surface, or arise as modifications from it. The conjugating gametes may be similar (e.g. Ectocarpus pusillus), or there may be a more or less pronounced difference of sex, an indication of which is found in Ectocarpus siliculosus (Fig. 66). When the gametes in this species have swarmed for a time, some, which are generally larger, are seen to attach themselves by one of the cilia, which by degrees is shortened to form a kind of stalk (compare the upper gamete in Fig. 66 II); these are the female gametes, which now become surrounded by a number of males endeavouring to conjugate with them, but only one succeeds in effecting fertilisation. The protoplasm of the two gametes coalesces (Fig. 66 III), and a zygote (e) is formed. The male gametes which do not conjugate may germinate, but the plants derived from them are much weaker than those produced by the zygotes. Strongly pronounced sexual differences are found in the Cutleriaceæ, in which order the male and female gametes arise in separate gametangia (Fig. 67 A). The male gametes (Fig. 67 D) are much smaller than the female gamete (Fig. 67 C); the latter, after swarming for a short time, withdraws the cilia, and is then ready to become fertilised (Fig. 67 B, E), thus we have here a distinct transition to the oogamous fertilisation which is found in the Fucaceæ. Alternation of generations is rarely found.

1. Sub-Family. Zoogonicæ.

Reproduction by means of gametes and zoospores.

Order 1. Ectocarpaceæ. The thallus consists of single or branched filaments with intercalary growth, extending vertically from a horizontal, branched filament or a disc, but sometimes it is reduced to this basal portion only. Zoosporangia and gametangia (for fertilisation see Fig. 66) are either outgrowths or arise by the transformation of one or several of the ordinary cells. The most common genera are: Ectocarpus and Pylaiella.

Order 2. Choristocarpaceæ. Choristocarpus, Discosporangium.

Order 3. Sphacelariaceæ. The thallus consists of small, parenchymatous, more or less ramified shoots, presenting a feather-like appearance. In the shoots, which grow by means of an apical cell (Fig. 68 S), a cortical layer, surrounding a row of central cells, is present. Sporangia and gametangia are outgrowths from the main stem or its branches. Sphacelaria, Chætopteris are common forms.

Order 16. Laminariaceæ. The thallus is more or less leathery, and has generally a root-like lower part (Fig. 69) which serves to attach it, and a stalk or stem-like part, terminated by a large leaf-like expansion. Meristematic cells are situated at the base of the leaf, and from these the new leaves are derived. The older leaf thus pushed away by the intercalary formation of the younger ones, soon withers (Fig. 69). Gametes are wanting. Zoosporangia are developed from the lower part of a simple, few-celled sporangiophore, which is an outgrowth from a surface-cell and has a large club-formed apical cell. The sporangia are aggregated into closely packed sori, which cover the lower part of the terminal leaf, or occur on special, smaller, lateral, fertile fronds (Alaria). Most of the species belonging to this order live in seas of moderate or cold temperature and occur in the most northern regions that have yet been explored, forming their organs of reproduction during the cold and darkness of the arctic night. Laminaria is destitute of a midrib and has only one terminal leaf. L. digitata has a broad leaf, which, by the violence of the waves, is torn into a number of palmate strips (Fig. 69). L. saccharina has a small, undivided leaf. Alaria has a midrib and special fertile fronds. A. esculenta occurs plentifully on the west coast of Norway and on the shores of Great Britain. Chorda filum, a common seaweed, is thick, unbranched, and attains a length of several metres, without any strong demarcation between stalk and leaf. Some attain quite a gigantic size, e.g. Macrocystis pyrifera, whose thallus is said sometimes to be more than 300 metres in length. The Lessonia-species, like the above, form submarine forests of seaweed on the south and south-west coasts of South America, the Cape, and other localities in the Southern Hemisphere.

Order 17. Cutleriaceæ. The thallus is formed by the union of the originally free, band-shaped shoots. The growth is intercalary. Sexual reproduction by the conjugation of male and female gametes. An asexual generation of different appearance, which produces zoospores, arises from the germination of the zygote. Cutleria, Zanardinia.

Sub-Family 2. Acinetæ.

Branched, simple cell-rows with intercalary growth. The organs of reproduction are partly uni-and partly multicellular; in the unicellular ones a cell without cilia is formed, which may be destitute of a cell-wall, but has one nucleus (oosphere?), or which has a cell-wall and contains several (generally four) nuclei (aplanospores?); in the multicellular, monosymmetric swarm-cells with two cilia (spermatozoids?) are formed. The fertilisation has not been observed.

Order 1. Tilopteridaceæ. Haplospora, Tilopteris.

Family 2. Cyclosporeæ.

The individuals are multicellular, with growth by an apical cell. The thallus—often bilateral—is differentiated into a root-like structure (attachment-disc), and stem, sometimes also into leaves (Sargassum). Sometimes a differentiation occurs into various tissue-systems, viz. an external assimilating tissue, a storing tissue, a mechanical tissue of thickened, longitudinal, parenchymatous, strengthening cells, and a conducting tissue of sieve-cells, or of short sieve-tubes with perforated walls. Colouring material, as in Phæosporeæ. Vegetative reproduction can only take place by means of detached portions of the thallus (Sargassum), which are kept floating by means of bladders (Fig. 70 A, a, Fig. 72). Zoospores are wanting.

The sexual reproduction takes place by oogamous fertilisation. The oogonia and antheridia are formed inside special organs (conceptacles), and are surrounded by paraphyses. The conceptacles (Fig. 70 B, Fig. 71 b) are small, pear-shaped or spherical depressions, produced by a special ingrowth of the surface cells of the thallus, and their mouths (ostioles) project like small warts; they are either situated near the end of the ordinary branches of the thallus (Fucus serratus, Fig. 71 a) which may be swollen on this account (Fucus vesiculosus, Fig. 70 A, b), or on special short branches (Ascophyllum, Sargassum). The vertical section of a conceptacle is seen in Fig. 70 B (see also Fig. 71 b) where, in addition to the paraphyses, oogonia only are seen (F. vesiculosus is diœcious—male plant, yellow-brown; female plant, olive-brown); but in some species antheridia, together with oogonia, are produced in the same conceptacle. The oogonia are large, almost spherical cells, situated on a short stalk, in each of which are formed from 1–8 (in Fucus, 8; in Ascophyllum, 4; in Halidrys, 1; in Pelvetia, 2) rounded, immotile oospheres. The wall of the oogonium ruptures, and the oospheres, still enclosed in the inner membrane, are ejected through the mouth of the conceptacle, and float about in the water, being finally set free by the bursting of the inner membrane. The antheridia are oblong cells (Fig. 70 C, a), many of which are produced on the same branched antheridiophore (Fig. 70 C); the numerous spermatozoids are provided with 2 cilia and are very small (Fig. 70 D, two antheridia surrounded by spermatozoids, one being open). The spermatozoids, still enclosed by the inner membrane of the antheridium, are similarly set free, and fertilisation takes place in the water, numerous spermatozoids collecting round the oosphere (Fig. 70 E), which is many times larger, and by their own motion causing it to rotate. After fertilisation, the oospore surrounds itself with a cell-wall and germinates immediately, attaching itself (Fig. 70 F) to some object, and by cell-division grows into a new plant.

Order 1. Fucaceæ. The following species are common on our coasts: Fucus vesiculosus (Fig. 70) has a thallus with an entire margin, and with bladders arranged in pairs; F. serratus (Fig. 71) without bladders, but with serrated margin; Ascophyllum nodosum has strap-like shoots, which here and there are swollen to form bladders; Halidrys siliquosa has its swimming bladders divided by transverse walls; Himanthalia lorea, which is found on the west coast of Norway, and the south coast of England, has a small perennial, button-shaped part, from the centre of which proceeds the long and sparsely branched, strap-like, annual shoot, which bears the conceptacles. The Gulf-weed (Sargassum bacciferum, Fig. 72) is well known historically from the voyage of Columbus; it is met with in large, floating, detached masses in all oceans, and is found most abundantly in the Atlantic, off the Canary Islands and the Azores, and towards the Bermudas. The stalked, spherical air-bladders are the characteristic feature of this genus. The thallus is more highly developed than in Fucus, and there is a contrast between the stem and leaf-like parts. The portions which are found floating are always barren, only those attached are fertile.

Class 9. Dictyotales.

The plants in this class are multicellular, and brown, with apical growth, new cells being derived either from a flat apical cell, or from a border of apical cells. The thallus is flat, leaf- or strap-shaped, attached by haptera, which are either found only at the base, or on the whole of the lower expansion of the thallus. The cells are differentiated into the following systems of tissues: an external, small-celled layer of assimilating cells, generally one cell in thickness, and an internal, large-celled layer of one or only a few cells in thickness, forming the mechanical and conducting tissues. All the reproductive cells are motionless. Asexual reproduction by naked, motionless spores (tetraspores) which are formed 1–4 in each tetrasporangium, the latter being outgrowths from the surface cells of special, sexless individuals. Zoospores are wanting. The sexual organs are of two kinds, oogonia and antheridia, which are formed from the surface cells, either on the same or different individuals. The oogonia are spherical or oval, and are generally placed close together; each contains one oosphere, which on maturity is ejected into the surrounding water, and is then naked and motionless. The antheridia are formed of longitudinal cells, united in groups, whose contents by repeated divisions—transverse and longitudinal—are divided into a large number of small, colourless, motionless spermatia—round or elongated—which are set free by the dissolution of the wall of the antheridium. The process of fertilisation has not yet been observed.

The Dictyotales, in having tetraspores and spermatia, deviate considerably from the Phæophyceæ, but may be classed near to the Tilopteridæ, in which there are asexual spores with 4 cell-nuclei, which may be considered as an indication of the formation of tetraspores.

Class 10. Rhodophyceæ (Red Seaweeds).

The plants comprised in this class are multicellular; they are simple or branched filaments, or expansions consisting of 1 to several layers of cells; the thallus may be differentiated (as in many Florideæ), to resemble stem, root, and leaf. The cells contain a distinctly differentiated nucleus (sometimes several), and distinct chromatophores, coloured by rhodophyll. The chlorophyll of the chromatophores is generally masked by a red colouring matter (phycoerythrin), which may be extracted in cold, fresh water; or rarely by phycocyan. Pyrenoids occur in some. Starch is never formed in the chromatophores themselves, but a modification—Florideæ starch—may be found in the colourless protoplasm. Asexual reproduction by motile or motionless spores (tetraspores) which are devoid of cilia and of cell-wall. Swarmspores are never found.

Sexual reproduction is wanting, or takes place by the coalescence of a spermatium and a more or less developed female cell. The spermatia are naked masses of protoplasm, devoid of cilia and chromatophores. The female cell (carpogonium) is enclosed by a cell-wall, and after fertilisation forms a number of spores, either with or without cell-walls (carpospores), which grow into new individuals.

The Rhodophyceæ may be divided into two families:

1. Bangioideæ.

2. Florideæ.

Family 1. Bangioideæ.

The thallus consists of a branched or unbranched cell-filament, formed of a single row or of many rows of cells, or of an expansion, one or two layers of cells in thickness, but without conspicuous pores for the intercommunication of the cells. The growth of the thallus is chiefly intercalary. The star-like chromatophores contain chlorophyll and are coloured blue-green with phycocyan, or reddish with phycoerythrin; all these colouring matters are occasionally found in the same cell (Bangia-species). Asexual reproduction by tetraspores, without cilia, but capable of amœboid movements.

Sexual reproduction is wanting, or takes place by the coalescence of a spermatium with a carpogonium, which is only slightly differentiated from the vegetative cells, and is devoid of a trichogyne. The carpospores are destitute of cell-wall and arise directly by the division of the fertilised oosphere. The Bangioideæ occur chiefly in salt water.