In biology, a spore is a unit of sexual (in fungi) or asexual reproduction that may be adapted for dispersal and for survival, often for extended periods of time, in unfavourable conditions. Spores form part of the life cycles of many plants, algae, fungi and protozoa.[1] They were thought to have appeared as early as the mid-late Ordovician period as an adaptation of early land plants.[2]
Bacterial spores are not part of a sexual cycle, but are resistant structures used for survival under unfavourable conditions.[3] Myxozoan spores release amoeboid infectious germs ("amoebulae") into their hosts for parasitic infection, but also reproduce within the hosts through the pairing of two nuclei within the plasmodium, which develops from the amoebula.[4]
In plants, spores are usually haploid and unicellular and are produced by meiosis in the sporangium of a diploid sporophyte. In some rare cases, diploid spore is also produced in some algae, or fungi.[5] Under favourable conditions, the spore can develop into a new organism using mitotic division, producing a multicellular gametophyte, which eventually goes on to produce gametes. Two gametes fuse to form a zygote, which develops into a new sporophyte. This cycle is known as alternation of generations.
The spores of seed plants are produced internally, and the megaspores (formed within the ovules) and the microspores are involved in the formation of more complex structures that form the dispersal units, the seeds and pollen grains.
The term spore derives from the ancient Greek word σπορά spora, meaning "seed, sowing", related to σπόρος Greek, Ancient (to 1453);: sporos, "sowing", and σπείρειν Greek, Ancient (to 1453);: speirein, "to sow".
In common parlance, the difference between a "spore" and a "gamete" is that a spore will germinate and develop into a sporeling, while a gamete needs to combine with another gamete to form a zygote before developing further.
The main difference between spores and seeds as dispersal units is that spores are unicellular, the first cell of a gametophyte, while seeds contain within them a developing embryo (the multicellular sporophyte of the next generation), produced by the fusion of the male gamete of the pollen tube with the female gamete formed by the megagametophyte within the ovule. Spores germinate to give rise to haploid gametophytes, while seeds germinate to give rise to diploid sporophytes.
Vascular plant spores are always haploid. Vascular plants are either homosporous (or isosporous) or heterosporous. Plants that are homosporous produce spores of the same size and type.
Heterosporous plants, such as seed plants, spikemosses, quillworts, and ferns of the order Salviniales produce spores of two different sizes: the larger spore (megaspore) in effect functioning as a "female" spore and the smaller (microspore) functioning as a "male". Such plants typically give rise to the two kind of spores from within separate sporangia, either a megasporangium that produces megaspores or a microsporangium that produces microspores. In flowering plants, these sporangia occur within the carpel and anthers, respectively.
Fungi commonly produce spores during sexual and asexual reproduction. Spores are usually haploid and grow into mature haploid individuals through mitotic division of cells (Urediniospores and Teliospores among rusts are dikaryotic). Dikaryotic cells result from the fusion of two haploid gamete cells. Among sporogenic dikaryotic cells, karyogamy (the fusion of the two haploid nuclei) occurs to produce a diploid cell. Diploid cells undergo meiosis to produce haploid spores.
Spores can be classified in several ways such as by their spore producing structure, function, origin during life cycle, and mobility.
Below is a table listing the mode of classification, name, identifying characteristic, examples, and images of different spore species.
| Mode of Classification | Name | Identifying Characteristic | Example Spore Containing Organism | Image | |
|---|---|---|---|---|---|
| Spore Producing Structure | Sporangiospore | Produced by sporangium | Zygomycetes | ||
| Zygospores | Produced by zygosporangium | Zygomycetes | |||
| Ascospores | Produced by ascus | Ascomycetes | |||
| Basidiospores | Produced by basidium | Basidiomycetes | |||
| Aecispores | Produced by aecium | Rusts and Smuts | |||
| Urediniospores | Produced by uredinium | Rusts and Smuts | |||
| Teliospores | Produced by teilum | Rusts and Smuts | |||
| Oospores | Produced by oogonium | Oomycetes | |||
| Carpospores | Produced by carposophorophyte | Red Algae | |||
| Tetraspores | Produced by tetrasphorophyte | Red Algae | |||
| Function | Chalmydospore | Thick-walled resting spores of fungi produced to survive in unfavorable conditions | Asomycota | ||
| Parasitic Fungal Spore | Internal Spores | Germinate within a host | |||
| External (Environmental) spores | Spores released by the host to infest other hosts [6] | ||||
| Origin During Life Cycle | Meiospores | Microspores | Produced sexually through meiosis, and give rise to a male gametophyte | Pollen in seed plants | |
| Megaspores (macrospores) | Produced sexually through meiosis, and give rise to a female gametophyte | Ovule in seed plants | |||
| Mitospores | Produced asexually though mitosis | Ascomycetes | |||
| Mobility | Zoospores | Mobile through flagella | Some algae and fungi | ||
| Aplanospores | Immobile, however still produce flagella | ||||
| Autospores | Immobile spores that do not produce flagella | ||||
| Ballistospores | Forcibly discharged from the fungal fruiting body due to internal force (such as built up pressure) | Basidiospores and/or part of the genus Pilobus | |||
| Stratismospores | Forcibly discharged from the fungal fruting body due to external force (such as raindrops or passing animals) | Puffballs | |||
Under high magnification, spores often have complex patterns or ornamentation on their exterior surfaces. A specialized terminology has been developed to describe features of such patterns. Some markings represent apertures, places where the tough outer coat of the spore can be penetrated when germination occurs. Spores can be categorized based on the position and number of these markings and apertures. Alete spores show no lines. In monolete spores, there is a single narrow line (laesura) on the spore.[7] Indicating the prior contact of two spores that eventually separated. In trilete spores, each spore shows three narrow lines radiating from a center pole.[7] This shows that four spores shared a common origin and were initially in contact with each other forming a tetrahedron. A wider aperture in the shape of a groove may be termed a colpus.[7] The number of colpi distinguishes major groups of plants. Eudicots have tricolpate spores (i.e. spores with three colpi).[8]
See main article: Evolutionary history of plants. Envelope-enclosed spore tetrads are taken as the earliest evidence of plant life on land,[9] dating from the mid-Ordovician (early Llanvirn, ~), a period from which no macrofossils have yet been recovered.[10] Individual trilete spores resembling those of modern cryptogamic plants first appeared in the fossil record at the end of the Ordovician period.[11]
In fungi, both asexual and sexual spores or sporangiospores of many fungal species are actively dispersed by forcible ejection from their reproductive structures. This ejection ensures exit of the spores from the reproductive structures as well as travelling through the air over long distances. Many fungi thereby possess specialized mechanical and physiological mechanisms as well as spore-surface structures, such as hydrophobins, for spore ejection. These mechanisms include, for example, forcible discharge of ascospores enabled by the structure of the ascus and accumulation of osmolytes in the fluids of the ascus that lead to explosive discharge of the ascospores into the air.[12]
The forcible discharge of single spores termed ballistospores involves formation of a small drop of water (Buller's drop), which upon contact with the spore leads to its projectile release with an initial acceleration of more than 10,000 g.[13] Other fungi rely on alternative mechanisms for spore release, such as external mechanical forces, exemplified by puffballs. Attracting insects, such as flies, to fruiting structures, by virtue of their having lively colours and a putrid odour, for dispersal of fungal spores is yet another strategy, most prominently used by the stinkhorns.
In Common Smoothcap moss (Atrichum undulatum), the vibration of sporophyte has been shown to be an important mechanism for spore release.[14]
In the case of spore-shedding vascular plants such as ferns, wind distribution of very light spores provides great capacity for dispersal. Also, spores are less subject to animal predation than seeds because they contain almost no food reserve; however they are more subject to fungal and bacterial predation. Their chief advantage is that, of all forms of progeny, spores require the least energy and materials to produce.
In the spikemoss Selaginella lepidophylla, dispersal is achieved in part by an unusual type of diaspore, a tumbleweed.[15]
Spores have been found in microfossils dating back to the mid-late Ordovician period.[16] Two hypothesized initial functions of spores relate to whether they appeared before or after land plants. The heavily studied hypothesis is that spores were an adaptation of early land plant species, such as embryophytes, that allowed for plants to easily disperse while adapting to their non-aquatic environment. [17] This is particularly supported by the observation of a thick spore wall in cryptospores. These spore walls would have protected potential offspring from novel weather elements. The second more recent hypothesis is that spores were an early predecessor of land plants and formed during errors in the meiosis of algae, a hypothesized early ancestor of land plants. [18]
Whether spores arose before or after land plants, their contributions to topics in fields like paleontology and plant phylogenetics have been useful. The spores found in microfossils, also known as cryptospores, are well preserved due to the fixed material they are in as well as how abundant and widespread they were during their respective time periods. These microfossils are especially helpful when studying the early periods of earth as macrofossils such as plants are not common nor well preserved. Both cryptospores and modern spores have diverse morphology that indicate possible environmental conditions of earlier periods of Earth and evolutionary relationships of plant species.