Alternation of generations

Alternation of generations is defined as the alternation of multicellular diploid and haploid forms in the organism's life cycle, regardless of whether these forms are free-living.^[6] In some species, such as the alga Ulva lactuca, the diploid and haploid forms are indeed both free-living independent organisms, essentially identical in appearance and therefore said to be isomorphic. In many algae, the free-swimming, haploid gametes form a diploid zygote which germinates into a multicellular diploid sporophyte. The sporophyte produces free-swimming haploid spores by meiosis that germinate into haploid gametophytes.^[7]

However, in land plants, either the sporophyte or the gametophyte is very much reduced and is incapable of free living. For example, in all bryophytes the gametophyte generation is dominant and the sporophyte is dependent on it. By contrast, in all seed plants the gametophytes are strongly reduced, although the fossil evidence indicates that they were derived from isomorphic ancestors.^[4] In seed plants, the female gametophyte develops totally within the sporophyte, which protects and nurtures it and the embryonic sporophyte that it produces. The pollen grains, which are the male gametophytes, are reduced to only a few cells (just three cells in many cases). Here the notion of two generations is less obvious; as Bateman & Dimichele say "sporophyte and gametophyte effectively function as a single organism".^[8] The alternative term 'alternation of phases' may then be more appropriate.^[9]

Initially, Adelbert von Chamisso (studying salps, colonial marine animals between 1815 and 1818^[10]) and Japetus Steenstrup (studying the development of trematodes in 1842, and also tunicates and cnidarians) described the succession of differently organized generations (sexual and asexual) in animals as "alternation of generations".^[11] Later, the phenomenon in animals became known as heterogamy, while the term "alternation of generations" was restricted to the life cycles of plants, meaning specifically the alternation of haploid gametophytes and diploid sporophytes.^[11]

In 1851, Wilhelm Hofmeister demonstrated the morphological alternation of generations in plants,^[12] between a spore-bearing generation (sporophyte) and a gamete-bearing generation (gametophyte).^[13][14] By that time, a debate emerged focusing on the origin of the asexual generation of land plants (i.e., the sporophyte) and is conventionally characterized as a conflict between theories of antithetic (Ladislav Josef Čelakovský, 1874) and homologous (Nathanael Pringsheim, 1876) alternation of generations.^[11]

In 1874, Eduard Strasburger discovered the alternation between diploid and haploid nuclear phases,^[11] also called cytological alternation of nuclear phases.^[15] Although most often coinciding, morphological alternation and nuclear phases alternation are sometimes independent of one another, e.g., in many red algae, the same nuclear phase may correspond to two diverse morphological generations.^[15] In some ferns which lost sexual reproduction, there is no change in nuclear phase, but the alternation of generations is maintained.^[16]

The diagram above shows the fundamental elements of the alternation of generations in plants. There are many variations in different groups of plants. The processes involved are as follows:^[17]

• Two single-celled haploid gametes, each containing n unpaired chromosomes, fuse to form a single-celled diploid zygote, which now contains n pairs of chromosomes, i.e. 2n chromosomes in total.^[17]
• The single-celled diploid zygote germinates, dividing by the normal process (mitosis), which maintains the number of chromosomes at 2n. The result is a multi-cellular diploid organism, called the sporophyte (because at maturity it produces spores).^[17]
• When it reaches maturity, the sporophyte produces one or more sporangia (singular: sporangium) which are the organs that produce diploid spore mother cells (sporocytes). These divide by a special process (meiosis) that reduces the number of chromosomes by a half. This initially results in four single-celled haploid spores, each containing n unpaired chromosomes.^[17]
• The single-celled haploid spore germinates, dividing by the normal process (mitosis), which maintains the number of chromosomes at n. The result is a multi-cellular haploid organism, called the gametophyte (because it produces gametes at maturity).^[17]
• When it reaches maturity, the gametophyte produces one or more gametangia (singular: gametangium) which are the organs that produce haploid gametes. At least one kind of gamete possesses some mechanism for reaching another gamete in order to fuse with it.^[17]

The 'alternation of generations' in the life cycle is thus between a diploid (2n) generation of multicellular sporophytes and a haploid (n) generation of multicellular gametophytes.^[17]

 

The situation is quite different from that in animals, where the fundamental process is that a multicellular diploid (2n) individual directly produces haploid (n) gametes by meiosis. In animals, spores (i.e. haploid cells which are able to undergo mitosis) are not produced, so there is no asexual multicellular generation. Some insects have haploid males that develop from unfertilized eggs, but the females are all diploid.^[17]

The diagram shown above is a good representation of the life cycle of some multi-cellular algae (e.g. the genus Cladophora) which have sporophytes and gametophytes of almost identical appearance and which do not have different kinds of spores or gametes.^[18]

However, there are many possible variations on the fundamental elements of a life cycle which has alternation of generations. Each variation may occur separately or in combination, resulting in a bewildering variety of life cycles. The terms used by botanists in describing these life cycles can be equally bewildering. As Bateman and Dimichele say "[...] the alternation of generations has become a terminological morass; often, one term represents several concepts or one concept is represented by several terms."^[19]

Possible variations are:

• Relative importance of the sporophyte and the gametophyte.
  • Equal (homomorphy or isomorphy).
    Filamentous algae of the genus Cladophora, which are predominantly found in fresh water, have diploid sporophytes and haploid gametophytes which are externally indistinguishable.^[20] No living land plant has equally dominant sporophytes and gametophytes, although some theories of the evolution of alternation of generations suggest that ancestral land plants did.
  • Unequal (heteromorphy or anisomorphy).

     

    • Dominant gametophyte (gametophytic).
      In liverworts, mosses and hornworts, the dominant form is the haploid gametophyte. The diploid sporophyte is not capable of an independent existence, gaining most of its nutrition from the parent gametophyte, and having no chlorophyll when mature.^[21]

       

    • Dominant sporophyte (sporophytic).
      In ferns, both the sporophyte and the gametophyte are capable of living independently, but the dominant form is the diploid sporophyte. The haploid gametophyte is much smaller and simpler in structure. In seed plants, the gametophyte is even more reduced (at the minimum to only three cells), gaining all its nutrition from the sporophyte. The extreme reduction in the size of the gametophyte and its retention within the sporophyte means that when applied to seed plants the term 'alternation of generations' is somewhat misleading: "[s]porophyte and gametophyte effectively function as a single organism".^[8] Some authors have preferred the term 'alternation of phases'.^[9]
• Differentiation of the gametes.
  • Both gametes the same (isogamy).
    Like other species of Cladophora, C. callicoma has flagellated gametes which are identical in appearance and ability to move.^[20]
  • Gametes of two distinct sizes (anisogamy).
    • Both of similar motility.
      Species of Ulva, the sea lettuce, have gametes which all have two flagella and so are motile. However they are of two sizes: larger 'female' gametes and smaller 'male' gametes.^[22]
    • One large and sessile, one small and motile (oogamy). The larger sessile megagametes are eggs (ova), and smaller motile microgametes are sperm (spermatozoa, spermatozoids). The degree of motility of the sperm may be very limited (as in the case of flowering plants) but all are able to move towards the sessile eggs. When (as is almost always the case) the sperm and eggs are produced in different kinds of gametangia, the sperm-producing ones are called antheridia (singular antheridium) and the egg-producing ones archegonia (singular archegonium).

       

      • Antheridia and archegonia occur on the same gametophyte, which is then called monoicous. (Many sources, including those concerned with bryophytes, use the term 'monoecious' for this situation and 'dioecious' for the opposite.^[23][24] Here 'monoecious' and 'dioecious' are used only for sporophytes.)
        The liverwort Pellia epiphylla has the gametophyte as the dominant generation. It is monoicous: the small reddish sperm-producing antheridia are scattered along the midrib while the egg-producing archegonia grow nearer the tips of divisions of the plant.^[25]
      • Antheridia and archegonia occur on different gametophytes, which are then called dioicous.
        The moss Mnium hornum has the gametophyte as the dominant generation. It is dioicous: male plants produce only antheridia in terminal rosettes, female plants produce only archegonia in the form of stalked capsules.^[26] Seed plant gametophytes are also dioicous. However, the parent sporophyte may be monoecious, producing both male and female gametophytes or dioecious, producing gametophytes of one gender only. Seed plant gametophytes are extremely reduced in size; the archegonium consists only of a small number of cells, and the entire male gametophyte may be represented by only two cells.^[27]
• Differentiation of the spores.
  • All spores the same size (homospory or isospory).
    Horsetails (species of Equisetum) have spores which are all of the same size.^[28]
  • Spores of two distinct sizes (heterospory or anisospory): larger megaspores and smaller microspores. When the two kinds of spore are produced in different kinds of sporangia, these are called megasporangia and microsporangia. A megaspore often (but not always) develops at the expense of the other three cells resulting from meiosis, which abort.
    • Megasporangia and microsporangia occur on the same sporophyte, which is then called monoecious.
      Most flowering plants fall into this category. Thus the flower of a lily contains six stamens (the microsporangia) which produce microspores which develop into pollen grains (the microgametophytes), and three fused carpels which produce integumented megasporangia (ovules) each of which produces a megaspore which develops inside the megasporangium to produce the megagametophyte. In other plants, such as hazel, some flowers have only stamens, others only carpels, but the same plant (i.e. sporophyte) has both kinds of flower and so is monoecious.

       

    • Megasporangia and microsporangia occur on different sporophytes, which are then called dioecious.
      An individual tree of the European holly (Ilex aquifolium) produces either 'male' flowers which have only functional stamens (microsporangia) producing microspores which develop into pollen grains (microgametophytes) or 'female' flowers which have only functional carpels producing integumented megasporangia (ovules) that contain a megaspore that develops into a multicellular megagametophyte.

There are some correlations between these variations, but they are just that, correlations, and not absolute. For example, in flowering plants, microspores ultimately produce microgametes (sperm) and megaspores ultimately produce megagametes (eggs). However, in ferns and their allies there are groups with undifferentiated spores but differentiated gametophytes. For example, the fern Ceratopteris thalictrioides has spores of only one kind, which vary continuously in size. Smaller spores tend to germinate into gametophytes which produce only sperm-producing antheridia.^[28]

 

Plant life cycles can be complex. Alternation of generations can take place in plants which are at once heteromorphic, sporophytic, oogametic, dioicous, heterosporic and dioecious, such as in a willow tree (as most species of the genus Salix are dioecious).^[29] The processes involved are:

• An immobile egg, contained in the archegonium, fuses with a mobile sperm, released from an antheridium. The resulting zygote is either male or female.
  • A male zygote develops by mitosis into a microsporophyte, which at maturity produces one or more microsporangia. Microspores develop within the microsporangium by meiosis.
    In a willow (like all seed plants) the zygote first develops into an embryo microsporophyte within the ovule (a megasporangium enclosed in one or more protective layers of tissue known as integument). At maturity, these structures become the seed. Later the seed is shed, germinates and grows into a mature tree. A male willow tree (a microsporophyte) produces flowers with only stamens, the anthers of which are the microsporangia.
  • Microspores germinate producing microgametophytes; at maturity one or more antheridia are produced. Sperm develop within the antheridia.
    In a willow, microspores are not liberated from the anther (the microsporangium), but develop into pollen grains (microgametophytes) within it. The whole pollen grain is moved (e.g. by an insect or by the wind) to an ovule (megagametophyte), where a sperm is produced which moves down a pollen tube to reach the egg.
  • A female zygote develops by mitosis into a megasporophyte, which at maturity produces one or more megasporangia. Megaspores develop within the megasporangium; typically one of the four spores produced by meiosis gains bulk at the expense of the remaining three, which disappear.
    Female willow trees (megasporophytes) produce flowers with only carpels (modified leaves that bear the megasporangia).
  • Megaspores germinate producing megagametophytes; at maturity one or more archegonia are produced. Eggs develop within the archegonia.
    The carpels of a willow produce ovules, megasporangia enclosed in integuments. Within each ovule, a megaspore develops by mitosis into a megagametophyte. An archegonium develops within the megagametophyte and produces an egg. The whole of the gametophytic generation remains within the protection of the sporophyte except for pollen grains (which have been reduced to just three cells contained within the microspore wall).

The term "plants" is taken here to mean the Archaeplastida, i.e. the glaucophytes, red and green algae and land plants.

Alternation of generations occurs in almost all multicellular red and green algae, both freshwater forms (such as Cladophora) and seaweeds (such as Ulva). In most, the generations are homomorphic (isomorphic) and free-living. Some species of red algae have a complex triphasic alternation of generations, in which there is a gametophyte phase and two distinct sporophyte phases. For further information, see Red algae: Reproduction.

Land plants all have heteromorphic (anisomorphic) alternation of generations, in which the sporophyte and gametophyte are distinctly different. All bryophytes, i.e. liverworts, mosses and hornworts, have the gametophyte generation as the most conspicuous. As an illustration, consider a monoicous moss. Antheridia and archegonia develop on the mature plant (the gametophyte). In the presence of water, the biflagellate sperm from the antheridia swim to the archegonia and fertilisation occurs, leading to the production of a diploid sporophyte. The sporophyte grows up from the archegonium. Its body comprises a long stalk topped by a capsule within which spore-producing cells undergo meiosis to form haploid spores. Most mosses rely on the wind to disperse these spores, although Splachnum sphaericum is entomophilous, recruiting insects to disperse its spores.

•  
  Alternation of generations in liverworts
•  
  Moss life cycle
•  
  Hornwort life cycle

The life cycle of ferns and their allies, including clubmosses and horsetails, the conspicuous plant observed in the field is the diploid sporophyte. The haploid spores develop in sori on the underside of the fronds and are dispersed by the wind (or in some cases, by floating on water). If conditions are right, a spore will germinate and grow into a rather inconspicuous plant body called a prothallus. The haploid prothallus does not resemble the sporophyte, and as such ferns and their allies have a heteromorphic alternation of generations. The prothallus is short-lived, but carries out sexual reproduction, producing the diploid zygote that then grows out of the prothallus as the sporophyte.

•  
  Alternation of generations in ferns
•  
  A gametophyte (prothallus) of Dicksonia
•  
  A sporophyte of Dicksonia antarctica
•  
  Dicksonia antarctica frond with spore-producing structures

In the spermatophytes, the seed plants, the sporophyte is the dominant multicellular phase; the gametophytes are strongly reduced in size and very different in morphology. The entire gametophyte generation, with the sole exception of pollen grains (microgametophytes), is contained within the sporophyte. The life cycle of a dioecious flowering plant (angiosperm), the willow, has been outlined in some detail in an earlier section (A complex life cycle). The life cycle of a gymnosperm is similar. However, flowering plants have in addition a phenomenon called 'double fertilization'. In the process of double fertilization, two sperm nuclei from a pollen grain (the microgametophyte), rather than a single sperm, enter the archegonium of the megagametophyte; one fuses with the egg nucleus to form the zygote, the other fuses with two other nuclei of the gametophyte to form 'endosperm', which nourishes the developing embryo.

It has been proposed that the basis for the emergence of the diploid phase of the life cycle (sporophyte) as the dominant phase (e.g. as in vascular plants) is that diploidy allows masking of the expression of deleterious mutations through genetic complementation.^[30][31] Thus if one of the parental genomes in the diploid cells contained mutations leading to defects in one or more gene products, these deficiencies could be compensated for by the other parental genome (which nevertheless may have its own defects in other genes). As the diploid phase was becoming predominant, the masking effect likely allowed genome size, and hence information content, to increase without the constraint of having to improve accuracy of DNA replication. The opportunity to increase information content at low cost was advantageous because it permitted new adaptations to be encoded. This view has been challenged, with evidence showing that selection is no more effective in the haploid than in the diploid phases of the lifecycle of mosses and angiosperms.^[32]

•  
  Angiosperm life cycle
•  
  Tip of tulip stamen showing pollen (microgametophytes)
•  
  Plant ovules (megagametophytes): gymnosperm ovule on left, angiosperm ovule (inside ovary) on right
•  
  Double fertilization

 

Some organisms currently classified in the clade Rhizaria and thus not plants in the sense used here, exhibit alternation of generations. Most Foraminifera undergo a heteromorphic alternation of generations between haploid gamont and diploid agamont forms. The diploid form is typically much larger than the haploid form; these forms are known as the microsphere and megalosphere, respectively.

Fungal mycelia are typically haploid. When mycelia of different mating types meet, they produce two multinucleate ball-shaped cells, which join via a "mating bridge". Nuclei move from one mycelium into the other, forming a heterokaryon (meaning "different nuclei"). This process is called plasmogamy. Actual fusion to form diploid nuclei is called karyogamy, and may not occur until sporangia are formed. Karogamy produces a diploid zygote, which is a short-lived sporophyte that soon undergoes meiosis to form haploid spores. When the spores germinate, they develop into new mycelia.

The life cycle of slime moulds is very similar to that of fungi. Haploid spores germinate to form swarm cells or myxamoebae. These fuse in a process referred to as plasmogamy and karyogamy to form a diploid zygote. The zygote develops into a plasmodium, and the mature plasmodium produces, depending on the species, one to many fruiting bodies containing haploid spores.

Alternation between a multicellular diploid and a multicellular haploid generation is never encountered in animals.^[33] In some animals, there is an alternation between parthenogenic and sexually reproductive phases (heterogamy), for instance in salps and doliolids (class Thaliacea). Both phases are diploid. This has sometimes been called "alternation of generations",^[34] but is quite different. In some other animals, such as hymenopterans, males are haploid and females diploid, but this is always the case rather than there being an alternation between distinct generations.

• Apomixis – Replacement of the normal sexual reproduction by asexual reproduction, without fertilization
• Evolutionary history of plants#life cycles: Evolutionary origin of the alternation of phases
• Ploidy – Number of sets of chromosomes of a cell

• Barnes, R.S.K.; Calow, P.; Olive, P.J.W.; Golding, D.W. & Spicer, J.I. (2001), The Invertebrates: a synthesis, Oxford; Malden, MA: Blackwell, ISBN 978-0-632-04761-1
• Bateman, R.M. & Dimichele, W.A. (1994), "Heterospory – the most iterative key innovation in the evolutionary history of the plant kingdom" (PDF), Biological Reviews of the Cambridge Philosophical Society, 69 (3): 345–417, doi:10.1111/j.1469-185x.1994.tb01276.x, S2CID 29709953, archived from the original (PDF) on 2012-04-15, retrieved 2010-12-30
• Bell, P.R. & Hemsley, A.R. (2000), Green Plants: their Origin and Diversity (2nd ed.), Cambridge, etc.: Cambridge University Press, ISBN 978-0-521-64109-8
• Foster, A.S. & Gifford, E.M. (1974), Comparative Morphology of Vascular Plants (2nd ed.), San Francisco: W.H. Freeman, ISBN 978-0-7167-0712-7
• Guiry, M.D.; Guiry, G.M. (2008), "Cladophora", AlgaeBase, World-wide electronic publication, National University of Ireland, Galway, retrieved 2011-07-21
• Kirby, A. (2001), Ulva, the sea lettuce, Monterey Bay Aquarium Research Institute, archived from the original on 2011-05-16, retrieved 2011-01-01
• Scott, Thomas (1996), Concise Encyclopedia Biology, Berlin: Walter de Gruyter, ISBN 978-3-11-010661-9
• Shyam, R. (1980), "On the life-cycle, cytology and taxonomy of Cladophora callicoma from India", American Journal of Botany, 67 (5): 619–24, doi:10.2307/2442655, JSTOR 2442655
• Sporne, K.R. (1974a), The Morphology of Angiosperms, London: Hutchinson, ISBN 978-0-09-120611-6
• Sporne, K.R. (1974b), The Morphology of Gymnosperms (2nd ed.), London: Hutchinson, ISBN 978-0-09-077152-3
• Stewart, W.N. & Rothwell, G.W. (1993), Paleobotany and the Evolution of Plants (2nd ed.), Cambridge, UK: Cambridge University Press, ISBN 978-0-521-38294-6
• Watson, E.V. (1981), British Mosses and Liverworts (3rd ed.), Cambridge, UK: Cambridge University Press, ISBN 978-0-521-28536-0
• Taylor, T.N.; Kerp, H. & Hass, H. (2005), "Life history biology of early land plants: Deciphering the gametophyte phase", Proceedings of the National Academy of Sciences of the United States of America, 102 (16): 5892–5897, Bibcode:2005PNAS..102.5892T, doi:10.1073/pnas.0501985102, PMC 556298, PMID 15809414