A lichen is a composite organism that arises from algae or cyanobacteria (or both) living among filaments of a fungus in a symbiotic relationship. The combined life form has properties that are very different from the properties of its component organisms. Lichens come in many colors, sizes, and forms. The properties are sometimes plant-like, but lichens are not plants. Lichens may have tiny, leafless branches (fruticose), flat leaf-like structures (foliose), flakes that lie on the surface like peeling paint (crustose), or other growth forms. A macrolichen is a lichen that is either bush-like or leafy; all other lichens are termed microlichens. Here, "macro" and "micro" do not refer to size, but to the growth form. Common names for lichens may contain the word "moss" (e.g., "Reindeer moss", "Iceland moss"), and lichens may superficially look like and grow with mosses, but lichens are not related to mosses or any plant.:3 Lichens do not have roots that absorb water and nutrients as plants do:2 but like plants they produce their own food by photosynthesis using sunlight energy, from carbon dioxide, water and minerals in their environment. When they grow on plants, they do not live as parasites and only use the plants as a substrate.
Lichens occur from sea level to high alpine elevations, in a very wide range of environmental conditions, and can grow on almost any surface. Lichens are abundant growing on bark, leaves, mosses, on other lichens, and hanging from branches "living on thin air" (epiphytes) in rain forests and in temperate woodland. They grow on bare rock, walls, gravestones, roofs, exposed soil surfaces, and in the soil as part of a biological soil crust. Different kinds of lichens have adapted to survive in some of the most extreme environments on Earth: arctic tundra, hot dry deserts, rocky coasts, and toxic slag heaps. They can even live inside solid rock, growing between the grains. Some lichens do not grow on anything, living out their lives blowing about the environment. It is estimated that 6% of Earth's land surface is covered by lichen. Colonies of lichens may be spectacular in appearance, dominating much of the surface of the visual landscape in forests and natural places, such as the vertical "paint" covering the vast rock faces of Yosemite National Park.:2
The fungus benefits from the symbiotic relation because algae or cyanobacteria produce food by photosynthesis. The algae or cyanobacteria benefit by being protected from the environment by the filaments of the fungus, which also gather moisture and nutrients from the environment, and (usually) provide an anchor to it. Lichenized fungus may refer to the entire lichen, or to the fungus growing in it. The lichen combination of fungus with algae and/or cyanobacteria has a very different form (morphology), physiology, and biochemistry to the component parts growing by themselves. Lichens are said to be "species", but what is meant by "species" is different from what is meant for plants, animals, and fungi, for which "species" implies a common ancestral lineage. Lichens are really combinations of species from two or three different biological kingdoms, so there is no common lineage. By convention, lichens have the same scientific name as the fungus in them, and are not classified according to the species of the algae and/or cyanobacteria growing in them. The alga or cyanobacterium has its own, unique, scientific name (binomial name). There are about 20,000 known species of lichens. Some lichens have lost the ability to reproduce sexually, yet continue to speciate. Recent perspectives on lichens include that they are relatively self-contained miniature ecosystems in and of themselves, possibly with more microorganisms living with the fungi, algae, and/or cyanobacteria, performing other functions as partners in a system that evolves as an even more complex composite organism (holobiont).
Lichens may be long-lived, with some considered to be among the oldest living things. They are among the first living things to grow on fresh rock exposed after an event such as a landslide. The long life-span and slow and regular growth rate of some lichens can be used to date events (lichenometry). Many lichens are very sensitive to environmental disturbances and can be used in cheaply assessing air pollution, ozone depletion, and metal contamination. Lichens have been used in making dyes, perfumes, and in traditional medicines. Few lichen species are eaten by insects or larger animals, such as reindeer.
- 1 Pronunciation
- 2 Growth forms
- 3 Physiology
- 3.1 Symbiotic relation
- 3.2 Reaction to water
- 3.3 Metabolites, metabolite structures and bioactivity
- 3.4 Substrate preference
- 3.5 Growth rate
- 3.6 Life span
- 3.7 Response to environmental stress
- 4 Reproduction and dispersal
- 5 Taxonomy and classification
- 6 Ecology and interactions with environment
- 7 Human use
- 8 History
- 9 Gallery
- 10 See also
- 11 References
- 12 Further reading
- 13 External links
Lichens grow in a wide range of shapes and forms (morphologies). The shape of a lichen is usually determined by the organization of the fungal filaments. The nonreproductive tissues, or vegetative body parts, is called the thallus. Lichens are grouped by thallus type, since the thallus is usually the most visually prominent part of the lichen. Thallus growth forms typically correspond to a few basic internal structure types. Common names for lichens often come from a growth form or color that is typical of a lichen genus.
Common groupings of lichen thallus growth forms are:
- fruticose – growing up like a tuft or multiply branched leafless mini-shrub, or hanging down in strands or tassles, 3-dimensional with a nearly round cross section for its branching parts (terete)
- foliose – growing in 2-dimensional, flat, leaf-like lobes that lift up from the surface
- crustose – crust-like, adhering tightly to a surface (substrate) like a thick coat of paint
- leprose – powdery
- gelatinous – jelly like
- filamentous – stringy or like matted hair
- byssoid – whispy, like teased wool
There are variations in growth types in a single lichen species, grey areas between the growth type descriptions, and overlapping between growth types, so some authors might describe lichens using different growth type descriptions.
When a crustose lichen gets old, the center may start to crack up like old-dried paint, old-broken asphalt paving, or like the polygonal "islands" of cracked-up mud in a dried lakebed. This is called being rimose or areolate, and the "island" pieces separated by the cracks are called areolas. The areolas appear separated, but are (or were) connected by an underlying "prothallus" or "hypothallus". When a crustose lichen grows from a center and appears to radiate out, it is called crustose placodioid. When the edges of the areolas lift up from the substrate, it is called squamulose.:159 Some people who study lichens (lichenologists) group squamulose lichens separately from crustose lichens.
These growth form groups are not precisely defined. Foliose lichens may sometimes branch and appear to be fruticose. Fruticose lichens may have flattened branching parts and appear leafy. Squamulous lichens may appear where the edges lift up. Gelatinous lichens may appear leafy when dry.:159 Means of telling them apart in these cases are in the sections below.
Structures involved in reproduction often appears as discs, bumps, or squiggly lines on the surface of the thallus.:4 The thallus is not always the part of the lichen that is most visually noticeable. Some lichens can grow inside solid rock between the grains (endolithic lichens), with only the sexual fruiting part visible growing outside the rock. These may be dramatic in color or appearance. Forms of these sexual parts are not in the above growth form categories. The most visually noticeable reproductive parts are often circular, raised, plate-like or disc-like outgrowths, with crinkly edges, and are described in sections below.
Lichens come in many colors.:4 Coloration is usually determined by the photosynthetic component. Special pigments, such as yellow usnic acid, give lichens a variety of colors, including reds, oranges, yellows, and browns, especially in exposed, dry habitats. In the absence of special pigments, lichens are usually bright green to olive gray when wet, gray or grayish-green to brown when dry. This is because moisture causes the surface skin (cortex) to become more transparent, exposing the green photobiont layer. Different colored lichens covering large areas of exposed rock surfaces, or lichens covering or hanging from bark can be a spectacular display when the patches of diverse colors "come to life" or "glow" in brilliant displays following rain.
Different colored lichens may inhabit different adjacent sections of a rock face, depending on the angle of exposure to light.
Color is used in identification.:4 Color changes depending on when a lichen is wet or dry. Color descriptions when used for identification are based on when the lichen is dry. Dry lichens with a cyanobacterium as the photosynthetic partner tend to be dark grey, brown, or black.
The underside of the leaf-like lobes of foliose lichens is a different color from the top side (dorsiventral), often brown or black, sometimes white. A fruticose lichen may have flattened "branches", appearing similar to a foiliose lichen, but the underside of a leaf-like structure on a fruticose lichen is the same color as the top side. The leaf-like lobes of a foliose lichen may branch, giving the appearance of a fruticose lichen, but the underside will be a different color from the top side.
Internal structure and growth forms
A lichen is made up of a simple photosynthesizing organism, usually green algae or cyanobacteria, surrounded by filaments of a fungus. Generally, most of a lichen's bulk is made of interwoven fungal filaments, although in filamentous and gelatinous lichens this is not the case. The fungus is called a mycobiont. The photosynthesizing organism is called a photobiont. Algal photobionts are called phycobionts. Cyanobacteria photobionts are called cyanobionts.
The part of a lichen that is not involved in reproduction, the "body" or "vegetative tissue" of a lichen, is called the thallus. The thallus form is very different from any form where the fungus or alga are growing separately. The thallus is made up of filaments of the fungus called hyphae. The filaments grow by branching then rejoining to create a mesh, which is called being "anastomose". The mesh of fungal filaments may be dense or loose.
Generally, the fungal mesh surrounds the algal or cyanobacterial cells, often enclosing them within complex fungal tissues that is unique to lichen associations. The thallus may or may not have a protective "skin" of densely packed fungal filaments, which is called a cortex. Fruticose lichens have one cortex layer wrapping around the "branches". Foliose lichens have an upper cortex on the top side of the "leaf", and a separate lower cortex on the bottom side. Crustose and squamulose lichens have only an upper cortex, with the "inside" of the lichen in direct contact with the surface they grow on (the substrate). Even if the edges peel up from the substrate and appear flat and leaf-like, they lack a lower cortex, unlike foliose lichens. Filamentous, byssoid, leprose, gelatinous, filimentous, and other lichens do not have a cortex, which is called being ecorticate.
Fruticose, foliose, crustose, and squamulose lichens generally have up to three different types of tissue, differentiated by having different densities of fungal filaments. The top layer, where the lichen contacts the environment, is called a cortex. The cortex is made of densely tightly woven, packed, and glued together (agglutinated) fungual filaments. The dense packing makes the cortex act like a protective "skin", keeping other organisms out, and reducing the intensity of sunlight on the layers below. The cortex layer can be up to several hundred micrometers (μm) in thickness (less than a millimeter). The cortex may be further topped by an epicortex of secretions, not cells, 0.6–1 μm thick in some lichens. This secretion layer may or may not have pores.
Below the cortex layer is a layer called the photobiontic layer or symbiont layer. The symbiont layer has less densely packed fungal filaments, with the photosynthetic partner embedded in them. The less dense packing allows air circulation during photosynthesis, similar to the anatomy of a leaf. Each cell or group of cells of the photobiont is usually individually wrapped by hyphae, and in some cases penetrated by an haustorium. In crustose and foliose lichens, algae in the photobiontic layer is diffuse among the fungal filaments, decreasing in gradation into the layer below. In fruticose lichens, the photobiontic layer is sharply distinct from the layer below.
The layer beneath the symbiont layer called is called the medulla. The medulla is less densely packed with fungal filaments than the layers above. In foliose lichens, there is (usually):159 another densely packed layer of fungal filaments called the lower cortex. Root-like fungal structures called rhizines (usually):159 grow from the lower cortex to attach or anchor the lichen to the substrate. Fruticose lichens have a single cortex wrapping all the way around the "stems" and "branches". The medulla is the lowest layer, and may form a cottony white inner core for the branchlike thallus, or it may be hollow.:159 Crustose and squamulose lichens lack a lower cortex, and the medulla is in direct contact with the substrate (biology) that the lichen grows on.
In crustose areolate lichens, the edges of the areolas peel up from the substrate and appear leafy. In squamulose lichens the part of the lichen thallus that is not attached to the substrate may also appear leafy. But these leafy parts lack a lower cortex, which distinguishes crustose and squamulose lichens from foliose lichens. Conversely, foliose lichens may appear flattened against the substrate like a crustose lichen, but most of the leaf-like lobes can be lifted up from the substrate because it is separated from it by a tightly packed lower cortex.
Gelatinous,:159 byssoid, and leprose lichens lack a cortex (are ecorticate), and generally have only undifferentiated tissue, similar to only having a symbiont layer.
In lichens that include both green algal and cyanobacterial symbionts, the cyanobacteria may be held on the upper or lower surface in small pustules called cephalodia.
A lichen is a composite organism that emerges from algae or cyanobacteria living among the filaments (hyphae) of a fungus in a mutually beneficial (symbiotic) relationship. The fungus benefits from the algae or cyanobacteria because they produce food by photosynthesis. The algae or cyanobacteria benefit by being protected from the environment by the filaments of the fungus, which also gather moisture and nutrients from the environment, and (usually) provide an anchor to it. Although some photosynthetic partners in a lichen can survive outside the lichen, the lichen symbiotic association extends the ecological range of both partners, whereby most descriptions of lichen associations describe them as symbiotic. Both partners gain water and mineral nutrients mainly from the atmosphere, through rain and dust. The fungal partner protects the alga by retaining water, serving as a larger capture area for mineral nutrients and, in some cases, provides minerals obtained from the substrate. If a cyanobacterium is present, as a primary partner or another symbiont in addition to a green alga as in certain tripartite lichens, they can fix atmospheric nitrogen, complementing the activities of the green alga.
The algal or cyanobacterial cells are photosynthetic and, as in plants, they reduce atmospheric carbon dioxide into organic carbon sugars to feed both symbionts. Phycobionts (algae) produce sugar alcohols (ribitol, sorbitol, and erythritol), which are absorbed by the mycobiont (fungus). Cyanobionts produce glucose. Lichenized fungal cells can make the photobiont "leak" out the products of photosynthesis, where they can then be absorbed by the fungus.:5
The lichen combination of alga and/or cyanobacterium with a fungus has a very different form (morphology), physiology, and biochemistry than the component fungus, alga, or cyanobacterium growing by itself, naturally or in culture. The body (thallus) of most lichens is different from those of either the fungus or alga growing separately. When grown in the laboratory in the absence of its photobiont, a lichen fungus develops as a structureless, undifferentiated mass of fungal filaments (hyphae). If combined with its photobiont under appropriate conditions, its characteristic form associated with the photobiont emerges, in the process called morphogenesis. In a few remarkable cases, a single lichen fungus can develop into two very different lichen forms when associating with either a green algal or a cyanobacterial symbiont. Quite naturally, these alternative forms were at first considered to be different species, until they were found growing in a conjoined manner.
Evidence that lichens are examples of successful symbiosis is the fact that lichens can be found in almost every habitat and geographic area on the planet. Two species in two genera of green algae are found in over 35% of all lichens, but can only rarely be found living on their own outside of a lichen.
In a case where one fungal partner simultaneously had two green algae partners that outperform each other in different climates, this might indicate having more than one photosynthetic partner at the same time might enable the lichen to exist in a wider range of habitats and geographic locations.
Algae produce sugars that are absorbed by the fungus by diffusion into special fungal hyphae called appressoria or haustoria in contact with the wall of the algal cells. The appressoria or haustoria may produce a substance that increases permeability of the algal cell walls, and may penetrate the walls. The algae may lose up to 80% of their sugar production to the fungus.
Debate over mutualism vs. commensalism and/or parasitism
Lichen associations may be examples of mutualism, commensalism or even parasitism, depending on the species. There is evidence to suggest that the lichen symbiosis is parasitic or commensalistic, rather than mutualistic. The photosynthetic partner can exist in nature independently of the fungal partner, but not vice versa. Photobiont cells are routinely destroyed in the course of nutrient exchange. The association is able to continue because reproduction of the photobiont cells matches the rate at which they are destroyed. The fungus surrounds the algal cells, often enclosing them within complex fungal tissues unique to lichen associations. In many species the fungus penetrates the algal cell wall, forming penetration pegs (haustoria) similar to those produced by fungi that feed on a host (pathogenic fungi). Cyanobacteria in laboratory settings can grow faster when they are alone rather than when they are part of a lichen.
Miniature ecosystem and holobiont theory
Symbiosis in lichens is so well-balanced that lichens have been considered to be relatively self-contained miniature ecosystems in and of themselves. It is thought that lichens may be even more complex symbiotic systems that include non-photosynthetic bacterial communities performing other functions as partners in a holobiont.
Some fungi can only be found living on lichens, and some only on those lichens (obligate parasites). These are referred to as lichenicolous fungi, which are a different species from the fungus living inside the lichen and are not considered to be part of the lichen.
Reaction to water
Moisture makes the cortex become more transparent.:4 This way, the algae can conduct photosynthesis when moisture is available, and is protected at other times. When the cortex is more transparent, the algae shows more clearly and the lichen looks greener.
Metabolites, metabolite structures and bioactivity
Secondary metabolites are thought to play a role in preference for some substrates over others.
Lichens often have a regular but very slow growth rate of less than a millimeter per year. Different lichen species have been measured to grow as slowly as 0.5 mm, and as fast as 0.5 meter per year.
Lichens may be long-lived (longevity), with some considered to be among the oldest living things. Lifespan is difficult to measure because the definition of what constitutes the "same" individual lichen is not precise. lichens grow by vegetatively having a piece break off, which may or may not be considered to be the "same" lichen, and because two lichens can grow into each other and then become the "same" lichen.
Response to environmental stress
Unlike simple dehydration in plants and animals, lichens may experience a complete loss of body water in dry periods. Lichens are capable of surviving extremely low levels of water content (poikilohydric). They quickly absorb water when it becomes available again, becoming soft and fleshy. Re-configuration of membranes following a period of dehydration requires several minutes or more.
In tests, lichen survived and showed remarkable results on the adaptation capacity of photosynthetic activity within the simulation time of 34 days under Martian conditions in the Mars Simulation Laboratory (MSL) maintained by the German Aerospace Center (DLR).
The European Space Agency has discovered that lichens can survive unprotected in space. In an experiment led by Leopoldo Sancho from the Complutense University of Madrid, two species of lichen—Rhizocarpon geographicum and Xanthoria elegans—were sealed in a capsule and launched on a Russian Soyuz rocket 31 May 2005. Once in orbit, the capsules were opened and the lichens were directly exposed to the vacuum of space with its widely fluctuating temperatures and cosmic radiation. After 15 days, the lichens were brought back to earth and were found to be in full health with no discernible damage from their time in orbit.
Reproduction and dispersal
Many lichens reproduce asexually, either by a piece breaking off and growing on its own (vegetative reproduction) or through the dispersal of diaspores containing a few algal cells surrounded by fungal cells. Because of the relative lack of differentiation in the thallus, the line between diaspore formation and vegetative reproduction is often blurred. Fruticose lichens can easily fragment, and new lichens can grow from the fragment (vegetative reproduction). Many lichens break up into fragments when they dry, dispersing themselves by wind action, to resume growth when moisture returns. Soredia (singular "soredium") are small groups of algal cells surrounded by fungal filaments that form in structures called soralia, from which the soredia can be dispersed by wind. Isidia (singular "isidium") are branched, spiny, elongated, outgrowths from the thallus that break off for mechanical dispersal. Lichen propagules (diaspores) typically contain cells from both partners, although the fungal components of so-called "fringe species" rely instead on algal cells dispersed by the "core species".
Structures involved in reproduction often appear as discs, bumps, or squiggly lines on the surface of the thallus.:4 Only the fungal partner in a lichen reproduces sexually. Many lichen fungi reproduce sexually like other fungi, producing spores formed by meiosis and fusion of gametes. Following dispersal, such fungal spores must meet with a compatible algal partner before a functional lichen can form. This may be a common form of reproduction in basidiolichens, which form fruiting bodies resembling their nonlichenized relatives.
Most lichen fungi belong to Ascomycetes (ascolichens). Among the ascolichens, spores are produced in spore-producing structures called ascomata. The most common types of ascomata are the apothecium (plural: apothecia) and perithecium (plural: perithecia).:14 Apothecia are usually cups or plate-like discs located on the top surface of the lichen thallus. When apothecia are shaped like squiggly line segments instead of like discs, they are called lirellae.:14 Perithecia are shaped like flasks that are immersed in the lichen thallus tissue, which has a small hole for the spores to escape the flask, and appear like black dots on the lichen surface.:14
The three most common spore body types being raised discs called apothecia (singular: apothecium), bottle-like cups with a small hole at the top called perithecia (singular: perithecium), and pycnidia (singular: pycnidium), shaped like perithecia but without asci (an ascus is the structure that contains and releases the sexual spores in fungi of the Ascomycota).
The apothecium has a layer of exposed spore-producing cells called asci (singular – ascus), and is usually a different color from the thallus tissue.:14 When the apothecium has an outer margin, the margin is called the exciple.:14 When the exciple has a color similar to colored thallus tissue the apothecium or lichen is called lecanorine, meaning similar to members of the genus Lecanora.:14 When the exciple is blackened like carbon it is called lecideine meaning similar to members of the genus Lecidea.:14 When the margin is pale or colorless it is called biatorine.:14
A "podetium" (plural podetia) is a lichenized stem-like structure of the fruiting body rising from the thallus, associated with some fungi that produce a fungal apothecium. Since it is part of the reproductive tissue, podetia are not considered part of the main body (thallus), but may be visually prominent. The podetium may be branched, and sometimes cup-like. They usually bear the fungal pycnidia or apothecia or both. Many lichens have apothecia that are visible to the naked eye.
Most lichens produce abundant sexual structures. Many species appear to disperse only by sexual spores. For example, the crustose lichens Graphis scripta and Ochrolechia parella produce no symbiotic vegetative propagules. Instead, the lichen-forming fungi of these species reproduce sexually by self-fertilization (i.e. they are homothallic). This breeding system may enable successful reproduction in harsh environments.
Mazaedia (singular – mazaedium) are apothecia shaped like a dressmaker's pin in (pin lichen)s, where the fruiting body is a brown or black mass of loose ascospores enclosed by a cup-shaped exciple, which sits on top of a tiny stalk.:15
Taxonomy and classification
Lichens are classified by the fungal component. Lichen species are given the same scientific name (binomial name) as the fungus species in the lichen. Lichens are being integrated into the classification schemes for fungi. The alga bears its own scientific name, which bears no relationship to that of the lichen or fungi. There are about 13,500–17,000 identified lichen species. Nearly 20% of known fungal species are associated with lichens.
"Lichenized fungus" may refer to the entire lichen, or to just the fungus. This may cause confusion without context. A particular fungus species may form lichens with different algae species, giving rise to what appear to be different lichen species, but which are still classified (as of 2014) as the same lichen species.
Formerly, some lichen taxonomists placed lichens in their own division, the Mycophycophyta, but this practice is no longer accepted because the components belong to separate lineages. Neither the ascolichens nor the basidiolichens form monophyletic lineages in their respective fungal phyla, but they do form several major solely or primarily lichen-forming groups within each phylum. Even more unusual than basidiolichens is the fungus Geosiphon pyriforme, a member of the Glomeromycota that is unique in that it encloses a cyanobacterial symbiont inside its cells. Geosiphon is not usually considered to be a lichen, and its peculiar symbiosis was not recognized for many years. The genus is more closely allied to endomycorrhizal genera.
Lichens independently emerged from fungi associating with algae and cyanobacteria at least twice in history.
The fungal component of a lichen is called the mycobiont. The mycobiont may be an Ascomycete or Basidiomycete. The associated lichens are called either ascolichens or basidiolichens, respectively. Living as a symbiont in a lichen appears to be a successful way for a fungus to derive essential nutrients since about 20% of all fungal species have acquired this mode of life.
Thalli produced by a given fungal symbiont with its differing partners may be similar, and the secondary metabolites identical, indicating that the fungus has the dominant role in determining the morphology of the lichen. But the same mycobiont with different photobionts may also produce very different growth forms. Lichens are known in which there is one fungus associated with two or even three algal species.
Although each lichen thallus generally appears homogeneous, some evidence seems to suggest that the fungal component may consist of more than one genetic individual of that species.
Two or more fungal species can interact to form the same lichen.
The photosynthetic partner in a lichen is called a photobiont. The photobiont in lichens come from a wide variety of simple prokaryotic and eukaryotic organisms. The majority of the lichens contain eukaryotic photobionts that are green algae (Chlorophyta) or yellow-green algae (Xanthophyta). The prokaryotes are blue green "algae" (cyanobacteria). Algal photobionts are called phycobionts. Cyanobacterium photobionts are called cyanobionts. About 90% of all known lichens have phycobionts, and about 10 have cyanobionts. Sometimes the photobiont is a green alga (chlorophyta) or other eukaryote, sometimes a blue-green "alga" (cyanobacteria, and sometimes both. Approximately 100 species of photosynthetic partners from 40 genera and five distinct classes (prokaryotic: Cyanophyceae; eukaryotic: Trebouxiophyceae, Phaeophyceae, Chlorophyceae) have been found to associate with the lichen-forming fungi.
Common algal photobionts are from the genus Trebouxia, Trentepohlia, Pseudotrebouxia, or Myrmecia (algae). Trebouxia is the most common genus of green algae in lichens, occurring in about 40% of all lichens. "Trebouxioid" means either a photobiont that is in the genus Trebouxia, or resembles a member of that genus, and is therefore presumably a member of the class Trebouxiophyceae. The second most commonly represented green alga genus is Trentepohlia. Overall, about 100 species of eukaryotes are known to occur as photobionts in lichens. All the algae are probably able to exist independently in nature as well as in the lichen.
A "cyanolichen" is a lichen with a cyanobacterium as its main photosynthetic component (photobiont). The most commonly occurring cyanobacteria genus is Nostoc. Other common cyanobacterium photobionts are from Scytonema. Many cyanolichens are small and black, and have limestone as the substrate. Another cyanolichen group, the jelly lichens (e.g., from the genera Collema or Leptogium) are large and foliose (e.g., species of Peltigera, Lobaria, and Degelia. These lichen species are grey-blue, especially when dampend or wet. Many of these characterize the Lobarion communities of higher rainfall areas in western Britain, e.g., in the Celtic Rainforest. Strains of cyanobacteria found in various cyanolichens are often closely related to one another. They differ from the most closely related free-living strains.
The lichen association is a close symbiosis. It extends the ecological range of both partners but is not always obligatory for their growth and reproduction in natural environments, since many of the algal symbionts can live independently. A prominent example is the alga Trentepohlia, which forms orange-coloured populations on tree trunks and suitable rock faces. Lichen propagules (diaspores) typically contain cells from both partners, although the fungal components of so-called "fringe species" rely instead on algal cells dispersed by the "core species".
The same cyanobiont species can occur in association with different fungal species as lichen partners. The same phycobiont species can occur in association with different fungal species as lichen partners. More than one phycobiont may be present in a single thallus.
Although each lichen thallus generally appears homogeneous, some evidence seems to suggest that the photobiont component may consist of more than one genetic individual of that species. A single lichen may contain several algal genotypes. These multiple genotypes may better enable response to adaptation to environmental changes, and enable the lichen to inhabit a wider range of environments.
Controversy over classification method and species names
There are about 20,000 known lichen species. But what is meant by "species" is different from what is meant by biological species in plants, animals, or fungi, where being the same species implies that there is a common ancestral lineage. Because lichens are combinations of members of two or even three different biological kingdoms, these components must have a different ancestral lineage from each other. By convention, lichens are still called "species" anyway, and are classified according to the species of their fungus, not the species of the algae or cyanobacteria. Lichens are given the same scientific name (binomial name) as the fungus in them, which may cause some confusion. The algae bears its own scientific name, which has no relationship to the name of the lichen or fungi.
Depending on context, "lichenized fungus" may refer to the entire lichen, or to the fungus when it is in the lichen, which can be grown in culture in isolation from the algae or cyanobacteria. Some algae and cyanobacteria are found naturally living outside of the lichen. The fungal, algal, or cyanobacterial component of a lichen can be grown by itself in culture. When growing by themselves, the fungus, algae, or cyanobacteria have very different properties than those of the lichen. Lichen properties such as growth form, physiology, and biochemistry, are very different from the combination of the properties of the fungus and the algae and/or cyanobacteria.
The same fungus growing in combination with different algae and/or cyanobacteria, can produce lichens that are very different in most properties, meeting non-DNA criteria for being different "species". Historically, these different combinations were classified as different species. When the fungus is identified as being the same using modern DNA methods, these apparently different species get reclassified as the same species under the current (2014) convention for classification by fungal component. This has led to debate about this classification convention. These apparently different "species" have their own independent evolutionary history.
There is also debate as to the appropriateness of giving the same binomial name to the fungus, and to the lichen that combines that fungus with an alga or cyanobacterium (synecdoche). This is especially the case when combining the same fungus with different algae or cyanobacteria produces dramatically different lichen organisms, which would be considered different species by any measure other than the DNA of the fungal component. If the whole lichen produced by the same fungus growing in association with different algae or cyanobacteria, were to be classified as different "species", the number of "lichen species" would be greater.
The largest number of lichenized fungi occur in the Ascomycota, with about 40% of species forming such an association. Some of these lichenized fungi occur in orders with nonlichenized fungi that live as saprotrophs or plant parasites (for example, the Leotiales, Dothideales, and Pezizales). Other lichen fungi occur in only five orders in which all members are engaged in this habit (Orders Graphidales, Gyalectales, Peltigerales, Pertusariales, and Teloschistales). Lichenized and nonlichenized fungi can even be found in the same genus or species. Overall, about 98% of lichens have an ascomycetous mycobiont. Next to the Ascomycota, the largest number of lichenized fungi occur in the unassigned fungi imperfecti, a catch-all category for fungi whose sexual form of reproduction has never been observed. Comparatively few Basidiomycetes are lichenized, but these include agarics, such as species of Lichenomphalia, clavarioid fungi, such as species of Multiclavula, and corticioid fungi, such as species of Dictyonema.
Lichen identification uses growth form and reactions to chemical tests.
"Pd" refers to the outcome of the Pd test or is used as an abbreviation for the chemical used in the test, para-phenylenediamine. If putting a drop on a lichen turns an area bright yellow to orange, this helps identify it as belonging to either the genus Cladonia or Lecanora.
Evolution and paleontology
The fossil record for lichens is poor. The extreme habitats that lichens dominate, such as tundra, mountains, and deserts, are not ordinarily conducive to producing fossils. There are fossilized lichens embedded in amber. The fossilized Anzia is found in pieces of amber in northern Europe and dates back approximately 40 million years. Lichen fragments are also found in fossil leaf beds, such as Lobaria from Trinity County in northern California, USA, dating back to the early to middle Miocene.
The oldest fossil lichens in which both symbiotic partners have been recovered date to the Early Devonian Rhynie chert, about 400 million years old. The slightly older fossil Spongiophyton has also been interpreted as a lichen on morphological and isotopic grounds, although the isotopic basis is decidedly shaky. It has been demonstrated that Silurian-Devonian fossils Nematothallus and Prototaxites were lichenized. Thus lichenized Ascomycota and Basidiomycota were a component of early Silurian-Devonian terrestrial ecosystems
The ancestral ecological state of both Ascomycota and Basidiomycota was probably saprobism, and independent lichenization events may have occurred multiple times. In 1995, Gargas and colleagues proposed that there were at least five independent origins of lichenization; three in the basidiomycetes and at least two in the Ascomycetes. However, Lutzoni et al. (2001) indicate that lichenization probably evolved earlier and was followed by multiple independent losses. Some non-lichen-forming fungi may have secondarily lost the ability to form a lichen association. As a result, lichenization has been viewed as a highly successful nutritional strategy.
Lichenized Glomeromycota may extend well back into the Precambrian. Winfrenatia, an early zygomycetous (Glomeromycota) lichen symbiosis that may have involved controlled parasitism, is permineralized in the Rhynie Chert of Scotland, of early Devonian age. Lichen-like fossils consisting of coccoid cells (cyanobacteria?) and thin filaments (mucoromycotinan Glomeromycota?) are permineralized in marine phosphorite of the Doushantuo Formation in southern China. These fossils are thought to be 551 to 635 million years old or Ediacaran. Ediacaran acritarchs also have many similarities with Glomeromycotan vesicles and spores. It has also been claimed that Ediacaran fossils including Dickinsonia, were lichens, although this claim is controversial. Endosymbiotic Glomeromycota comparable with living Geosiphon may extend back into the Proterozoic in the form of 1500 million year old Horodyskia and 2200 million year old Diskagma. Discovery of these fossils suggest that fungi developed symbiotic partnerships with photoautotrophs long before the evolution of vascular plants.
Ecology and interactions with environment
Substrates and habitats
Lichens grow in a wide range of substrates and habitats, including some of the most extreme conditions on earth. They are abundant growing on bark, leaves, and hanging from branches "living on thin air" (epiphytes) in rain forests and in temperate woodland. They grow on bare rock, walls, gravestones, roofs, exposed soil surfaces. They can survive in some of the most extreme environments on Earth: arctic tundra, hot dry deserts, rocky coasts, and toxic slag heaps. They can even live inside solid rock, growing between the grains, and in the soil as part of a biological soil crust in arid habitats such as deserts. Some lichens do not grow on anything, living out their lives blowing about the environment.
When growing on mineral surfaces, some lichens slowly decompose their substrate by chemically degrading and physically disrupting the minerals, contributing to the process of weathering by which rocks are gradually turned into soil. While this contribution to weathering is usually benign, it can cause problems for artificial stone structures. For example, there is an ongoing lichen growth problem on Mount Rushmore National Memorial that requires the employment of mountain-climbing conservators to clean the monument.
Lichens are not parasites on the plants they grow on, but only use them as a substrate to grow on. The fungi of some lichen species may "take over" the algae of other lichen species. Lichens make their own food from their photosynthetic parts and by absorbing minerals from the environment. Lichens growing on leaves may have the appearance of being parasites on the leaves, but they are not. However, some lichens, notably those of the genus Diploschistes are known to parasitise other lichens. Diploschistes muscorum starts its development in the tissue of a host Cladonia species.:30:171
In the arctic tundra, lichens, together with mosses and liverworts, make up the majority of the ground cover, which helps insulate the ground and may provide forage for grazing animals. An example is "Reindeer moss", which is a lichen, not a moss.
A crustose lichen that grows on rock is called a saxicolous lichen.:159 Crustose lichens that grow on the rock are epilithic, and those that grow immersed inside rock, growing between the crystals with only their fruiting bodies exposed to the air, are called endolithic lichens.:159 A crustose lichen that grows on bark is called a corticolous lichen.:159 A lichen that grows on wood from which the bark has been stripped is called a lignicolous lichen. Lichens that grow immersed inside plant tissues are called endophloidic lichens or endophloidal lichens.:159 Lichens that use leaves as substrates, whether the leaf is still on the tree or on the ground, are called epiphyllous or foliicolous. A terricolous lichen grows on the soil as a substrate. Many squamulous lichens are terricolous.:159 Umbillicate lichens are foliose lichens that are attached to the substrate at only one point. A vagrant lichen is not attached to a substrate at all, and lives its life being blown around by the wind.
Lichens and soils
In addition to distinct physical mechanisms by which lichens break down raw stone, recent studies indicate lichens attack stone chemically, entering newly chelated minerals into the ecology.
The lichen exudates, which have powerful chelating capacity, the widespread occurrence of mineral neoformation, particularly metal oxalates, together with the characteristics of weathered substrates, all confirm the significance of lichens as chemical weathering agents.
Over time, this activity creates new fertile soil from lifeless stone.
Lichens may be important in contributing nitrogen to soils in some deserts through being eaten, along with their rock substrate, by snails, which then defecate, putting the nitrogen into the soils. Lichens help bind and stabilize soil sand in dunes. In deserts and semi-arid areas, lichens are part of extensive, living biological soil crusts, essential for maintaining the soil structure. Lichens have a long fossil record in soils dating back 2.2 billion years.
Lichens are pioneer species, among the first living things to grow on bare rock or areas denuded of life by a disaster. Lichens may have to compete with plants for access to sunlight, but because of their small size and slow growth, they thrive in places where higher plants have difficulty growing. Lichens are often the first to settle in places lacking soil, constituting the sole vegetation in some extreme environments such as those found at high mountain elevations and at high latitudes. Some survive in the tough conditions of deserts, and others on frozen soil of the Arctic regions.
A major ecophysiological advantage of lichens is that they are poikilohydric (poikilo- variable, hydric- relating to water), meaning that though they have little control over the status of their hydration, they can tolerate irregular and extended periods of severe desiccation. Like some mosses, liverworts, ferns, and a few "resurrection plants", upon desiccation, lichens enter a metabolic suspension or stasis (known as cryptobiosis) in which the cells of the lichen symbionts are dehydrated to a degree that halts most biochemical activity. In this cryptobiotic state, lichens can survive wider extremes of temperature, radiation and drought in the harsh environments they often inhabit.
Lichens do not have roots and do not need to tap continuous reservoirs of water like most higher plants, thus they can grow in locations impossible for most plants, such as bare rock, sterile soil or sand, and various artificial structures such as walls, roofs and monuments. Many lichens also grow as epiphytes (epi- on the surface, phyte- plant) on plants, particularly on the trunks and branches of trees. When growing on plants, lichens are not parasites; they do not consume any part of the plant nor poison it. Lichens produce allelopathic chemicals that inhibit the growth of mosses. Some ground-dwelling lichens, such as members of the subgenus Cladina (reindeer lichens), produce allelopathic chemicals that leach into the soil and inhibit the germination of seeds, spruce and other plants. Stability (that is, longevity) of their substrate is a major factor of lichen habitats. Most lichens grow on stable rock surfaces or the bark of old trees, but many others grow on soil and sand. In these latter cases, lichens are often an important part of soil stabilization; indeed, in some desert ecosystems, vascular (higher) plant seeds cannot become established except in places where lichen crusts stabilize the sand and help retain water.
Lichens may be eaten by some animals, such as reindeer, living in arctic regions. The larvae of a number of Lepidoptera species feed exclusively on lichens. These include Common Footman and Marbled Beauty. However, lichens are very low in protein and high in carbohydrates, making them unsuitable for some animals. Lichens are also used by the Northern Flying Squirrel for nesting, food, and a water source during winter.
Effects of air pollution
If lichens are exposed to air pollutants at all times, without any deciduous parts, they are unable to avoid the accumulation of pollutants. Also lacking stomata and a cuticle, lichens may absorb aerosols and gases over the entire thallus surface from which they may readily diffuse to the photobiont layer. Because lichens do not possess roots, their primary source of most elements is the air, and therefore elemental levels in lichens often reflect the accumulated composition of ambient air. The processes by which atmospheric deposition occurs include fog and dew, gaseous absorption, and dry deposition. Consequently, many environmental studies with lichens emphasize their feasibility as effective biomonitors of atmospheric quality.
Not all lichens are equally sensitive to air pollutants, so different lichen species show different levels of sensitivity to specific atmospheric pollutants. The sensitivity of a lichen to air pollution is directly related to the energy needs of the mycobiont, so that the stronger the dependency of the mycobiont on the photobiont, the more sensitive the lichen is to air pollution. Upon exposure to air pollution, the photobiont may use metabolic energy for repair of its cellular structures that would otherwise be used for maintenance of its photosynthetic activity, therefore leaving less metabolic energy available for the mycobiont. The alteration of the balance between the photobiont and mycobiont can lead to the breakdown of the symbiotic association. Therefore, lichen decline may result not only from the accumulation of toxic substances, but also from altered nutrient supplies that favor one symbiont over the other.
Lichens are eaten by many different cultures across the world. Although some lichens are only eaten in times of famine, others are a staple food or even a delicacy. Two obstacles are often encountered when eating lichens: lichen polysaccharides are generally indigestible to humans, and lichens usually contain mildly toxic secondary compounds that should be removed before eating. Very few lichens are poisonous, but those high in vulpinic acid or usnic acid are toxic. Most poisonous lichens are yellow.
In the past Iceland moss (Cetraria islandica) was an important human food in northern Europe, and was cooked as a bread, porridge, pudding, soup, or salad. Wila (Bryoria fremontii) was an important food in parts of North America, where it was usually pitcooked. Northern peoples in North America and Siberia traditionally eat the partially digested reindeer lichen (Cladina spp.) after they remove it from the rumen of caribou or reindeer that have been killed. Rock tripe (Umbilicaria spp. and Lasalia spp.) is a lichen that has frequently been used as an emergency food in North America, and one species, Umbilicaria esculenta, is used in a variety of traditional Korean and Japanese foods.
Lichenometry is a technique used to determine the age of exposed rock surfaces based on the size of lichen thalli. Introduced by Beschel in the 1950s, the technique has found many applications. it is used in archaeology, palaeontology, and geomorphology. It uses the presumed regular but slow rate of lichen growth to determine the age of exposed rock.:9 Measuring the diameter (or other size measurement) of the largest lichen of a species on a rock surface indicates the length of time since the rock surface was first exposed. Lichen can be preserved on old rock faces for up to 10,000 years, providing the maximum age limit of the technique, though it is most accurate (within 10% error) when applied to surfaces that have been exposed for less than 1,000 years. Lichenometry is especially useful for dating surfaces less than 500 years old, as radiocarbon dating techniques are less accurate over this period. The lichens most commonly used for lichenometry are those of the genera Rhizocarpon (e.g. the species Rhizocarpon geographicum) and Xanthoria.
Lichens have been shown to degrade polyester resins, as can be seen in archaeological sites in the Roman city of Baelo Claudia Spain. Lichens can accumulate several environmental pollutants such as lead, copper, and radionuclides.
Many lichens produce secondary compounds, including pigments that reduce harmful amounts of sunlight and powerful toxins that reduce herbivory or kill bacteria. These compounds are very useful for lichen identification, and have had economic importance as dyes such as cudbear or primitive antibiotics.
In the Highlands of Scotland, traditional dyes for Harris tweed and other traditional cloths were made from lichens including the orange Xanthoria parietina and the grey foliaceous Parmelia saxatilis common on rocks known as "crottle".
There are reports dating almost 2000 years old of lichens being used to make purple and red dyes. Of great historical and commercial significance are lichens belonging to the family Roccellaceae, commonly called orchella weed or orchil. Orcein and other lichen dyes have largely been replaced by synthetic versions.
Lichens produce metabolites proven useful in the medical community. Most metabolites produced by lichens are structurally and functionally similar to broad-spectrum antibiotics while few are associated respectively to antiseptic similarities. These organic acids are the metabolic byproducts of Crassulacean acid metabolism, the means of photosynthesis by lichens.
Usnic acid is the most commonly studied metabolite produced by lichens and has been associated with the suppression of tuberculosis. It has also proven bactericidal against Escherichia coli and Staphylococcus aureus and is considered an antimicrobial agent. It is still unclear if the antimicrobial processes derived from lichens are strictly due to their metabolites or their symbiotic relationship with the fungi that grows on it.
Colonies of lichens may be spectacular in appearance, dominating the surface of the visual landscape as part of the aesthetic appeal to paying visitors of Yosemite National Park and Sequoia National Park.:2 Orange and yellow lichens add to the ambience of desert trees, rock faces, tundras, and rocky seashores. Intricate webs of lichens hanging from tree branches add a mysterious aspect to forests. Fruticose lichens are used in model railroading and other modeling hobbies as a material for making miniature trees and shrubs.
Lichens have been used in nonscientific traditional medicine practices of many cultures. Historically in Europe, Lobaria pulmonaria was collected in large quantities as "Lungwort", due to its lung-like appearance (see doctrine of signatures). Similarly Peltigera leucophlebia was used as a supposed cure for thrush, due to the resemblance of its cephalodia to the appearance of the disease.
Potential application in treating Mad Cow Disease
Although lichens had been recognized as organisms for quite some time, it was not until 1867, when Swiss botanist Simon Schwendener proposed his dual theory of lichens, that lichens are a combination of fungi with algae or cyanobacteria, whereby the true nature of the lichen association began to emerge. Schwendener's hypothesis, which at the time lacked experimental evidence, arose from his extensive analysis of the anatomy and development in lichens, algae, and fungi using a light microscope. Many of the leading lichenologists at the time, such as James Crombie and Nylander, rejected Schwendener's hypothesis because the common consensus was that all living organisms were autonomous.
Other prominent biologists, such as Heinrich Anton de Bary, Albert Bernhard Frank, Melchior Treub and Hermann Hellriegel were not so quick to reject Schwendener's ideas and the concept soon spread into other areas of study, such as microbial, plant, animal and human pathogens. When the complex relationships between pathogenic microorganisms and their hosts were finally identified, Schwendener's hypothesis began to gain popularity. Further experimental proof of the dual nature of lichens was obtained when Eugen Thomas published his results in 1939 on the first successful re-synthesis experiment.
Xanthoparmelia cf. lavicola, a foliose lichen, on basalt.
Map lichen (Rhizocarpon geographicum) on rock
Reindeer moss (Cladonia rangiferina)
Lecanora cf. muralis lichen on the banks of the Bega canal in Timișoara
Caloplaca marina, a marine lichen
Microscopic view of lichen growing on a piece of concrete dust.
- "What is a lichen?, Australian National Botanical Garden". Retrieved 10 October 2014.
- Introduction to Lichens - An Alliance between Kingdoms, University of California Museum charity's Williams of Paleontology, 
- Lichens of North America, Irwin M. Brodo, Ms. Sylvia Duran Sharnoff, ISBN 978-0300082494, 2001
- Lichen Glossary, Australian National Botanic Garden
- "Looking at Lichens", Lynn Margulis, Eva Barreno, BioScience 53(8):776–778 2003, 
- Field Guide to California Lichens, Stephen Sharnoff, Yale University Press, 2014, ISBN 978-0-300-19500-2
- Speer, Brian R; Ben Waggoner (May 1997). "Lichens: Life History & Ecology". University of California Museum of Paleontology. Retrieved 28 April 2015.
- Geoffrey Michael Gadd (March 2010). "Metals, minerals and microbes: geomicrobiology and bioremediation". Microbiology 156 (Pt 3): 609–643. doi:10.1099/mic.0.037143-0. PMID 20019082.
- McCune, B.; Grenon, J.; Martin, E.; Mutch, L.S.; Martin, E.P. (Mar 2007). "Lichens in relation to management issues in the Sierra Nevada national parks". North American Fungi 2: 1–39. doi:10.2509/pnwf.2007.002.003.
- "Lichens: Systematics, University of California Museum of Paleontology". Retrieved 10 October 2014.
- "A taxonomic revision of the North American species of Lepraria s.l. that produce divaricatic acid, with notes on the type species of the genus L. incana, James C. Lendemer, Mycologia 103(6): 1216–1229, 
- "Two Trebouxia algae with different physiological performances are ever-present in lichen thalli of Ramalina farinacea. Coexistence versus Competition?", Leonardo M. Casano, Eva M. del Campo, Francisco J. García-Breijo, José Reig-Armiñana, Francisco Gasulla, Alicia del Hoyo, Alfredo Guéra1, and Eva Barreno, Environmental Microbiology (2011) 13(3), 
- Honegger, R. (1991) Fungal evolution: symbiosis and morphogenesis, Symbiosis as a Source of Evolutionary Innovation, Margulis, L., and Fester, R. (eds). Cambridge, MA, USA: The MIT Press, pp. 319–340.
- Species-speciﬁc structural and functional diversity of bacterial communities in lichen symbiosis. ; Grube, M., Cardinale, M., Vieira de Castro, J., Müller, H., and Berg, G.; The ISME Journal 3: 1105–1115, 2009
- "Non photosynthetic bacteria associated to cortical structures on Ramalinaand Usnea thalli from Mexico"; Barreno, E., Herrera-Campos, M., García-Breijo, F., Gasulla, F., and Reig-Armiñana, J. (2008); Asilomar, Paciﬁc Grove, CA, USA: Abstracts IAL 6- ABLS Joint Meeting, pp 5., .
- Morris J, Purvis W. (2007). Lichens (Life). London: The Natural History Museum. p. 19. ISBN 0-565-09153-0.
- Ferry, B. W., Baddeley, M. S. & Hawkworth, D. L. (editors) (1973) Air Pollution and Lichens. Athlone Press, London.
- Rose C. I., Hawksworth D. L.; Hawksworth (1981). "Lichen recolonization in London's cleaner air". Nature 289 (5795): 289–292. Bibcode:1981Natur.289..289R. doi:10.1038/289289a0.
- D.L. Hawksworth and F. Rose(1976) Lichens as pollution monitors. Edward Arnold, Institute of Biology Series, No. 66. 60pp. ISBN 0713125551 (pbk.)
- Oak Moss Absolute, Vitorie, Inc.
- "Wild reindeer foraging-niche organization" Terje Skogland, Ecography 7(4): 345-379 1984 
- Lichen, The Spectator, Dot Wordsworth, 17 November 2012
- Lichens, Horticultural and Home Pest News, Iowa State University
- "Lichens: Fungi Algae and Bacteria Work together", Kevin Fitzgerald, Sciences 360, 
- "Lichen". Oxford Dictionaries. Retrieved 2014-11-02.
- "Lichens and Bryophytes, Michigan State University, 10-25-99". Retrieved 10 October 2014.
- Lichen Vocabulary, Lichens of North America Information, Sylvia and Stephen Sharnoff, 
- "Alan Silverside's Lichen Glossary (p-z), Alan Silverside". Retrieved 10 October 2014.
- "Fioliose lichens, Lichen Thallus Types, Allan Silverside". Retrieved 10 October 2014.
- Mosses Lichens & Ferns of Northwest North America, Dale H. Vitt, Janet E. Marsh, Robin B. Bovey, Lone Pine Publishing Company, ISBN 0-295-96666-1
- "Lichens, Saguaro-Juniper Corporation". Retrieved 10 October 2014.
- Michigan Lichens, Julie Jones Medlin, B. Jain Publishers, 1996, ISBN 0877370397, 9780877370390, 
- Lichens: More on Morphology, University of California Museum of Paleontology, 
- Lichen Photobionts, University of Nebraska Omaha
- "Alan Silverside's Lichen Glossary (g-o), Alan Silverside". Retrieved 10 October 2014.
- Büdel, B.; Scheidegger, C. (1996). "Thallus morphology and anatomy". Lichen Biology: 37–64.
- "Pruina as a Taxonomic Character of the Lichen Genus Dermatocarpon", Starri Heidmarsson, The Bryologist' Vol. 99, No. 3 (Autumn 1996), pp. 315–320, 
- "Lichen Biology and the Environment", Lichens of North America Information, Sylvia and Stephen Sharnoff, 
- Brodo, Sharnoff & Sharnoff, 2001
- "Evolutionary inferences based on ITS rDNA and actin sequences reveal extensive diversity of the common lichen alga Asterochloris (Treboux- iophyceae, Chlorophyta), Skaloud, P., and Peksa, O. (2010). Mol Phylogenet Evol 54: 36–46
- Gordon Ramel. "What is a Lichen?". Earthlife Web,. Retrieved 20 January 2015.
- Ahmadjian 1993
- F.S. Dobson (2000) Lichens, an illustrated guide to the British and Irish species. Richmond Publishing Co. Ltd., Slough, UK
- R. Honegger (1988) Mycobionts. Chapter 3 in T. H. Nash (ed.) (1996) Lichen Biology. Cambridge University Press. ISBN 0-521-45368-2
- "Lichenicolous Fungi: Interactions, Evolution, and Biodiversity", James D. Lawrey, Paul Diederich, The Bryologist 106(1), pp. 80 120, 2003, 
- Hagiwara K, Wright PR, et al. (March 2015). "Comparative analysis of the antioxidant properties of Icelandic and Hawaiian lichens". Environmental Microbiology. doi:10.1111/1462-2920.12850. PMID 25808912.
- Odabasoglu F, Aslan A, Cakir A, et al. (March 2005). "Antioxidant activity, reducing power and total phenolic content of some lichen species". Fitoterapia 76 (2): 216–9. doi:10.1016/j.fitote.2004.05.012. PMID 15752633.
- "Norstictic acid: Correlations between its physico-chemical characteristics and ecological preferences of lichens producing this depsidone", Markus Hauck, Sascha-René Jürgens, Christoph Leuschner, Environmental and Experimental Botany, Volume 68, Issue 3, May 2010, Pages 309–313, 
- Growth and Development in Lichens, Earthlife Net
- "Lichens in Yellowstone National Park", Sharon Eversman, Yellowstone Science 15(3), 2007, National Park Service, 
- Nash, Thomas H., ed. (2008). Lichen Biology (2nd ed.). Cambridge University Press. pp. 5–6. ISBN 978-0-521-69216-8.
- Baldwin, Emily (26 April 2012). "Lichen survives harsh Mars environment". Skymania News. Retrieved 27 April 2012.
- de Vera, J.-P.; Kohler, Ulrich (26 April 2012). "The adaptation potential of extremophiles to Martian surface conditions and its implication for the habitability of Mars" (PDF). European Geosciences Union. Retrieved 27 April 2012.
- "ESA — Human Spaceflight and Exploration - Lichen survives in space". Retrieved 2010-02-16.
- Sancho, L. G.; De La Torre, R.; Horneck, G.; Ascaso, C.; De Los Rios, A.; Pintado, A.; Wierzchos, J.; Schuster, M. (2007). "Lichens survive in space: results from the 2005 LICHENS experiment". Astrobiology 7 (3): 443–54. Bibcode:2007AsBio...7..443S. doi:10.1089/ast.2006.0046. PMID 17630840.
- Eichorn, Susan E., Evert, Ray F., and Raven, Peter H. 2005. Biology of Plants. New York: W. H. Freeman and Company. 289 p. 1.
- Cook, Rebecca and McFarland, Kenneth. 1995. General Botany 111 Laboratory Manual. Knoxville (TN): University of Tennessee. 104 p.
- A. N. Rai; B. Bergman; Ulla Rasmussen (31 July 2002). Cyanobacteria in Symbiosis. Springer. p. 59. ISBN 978-1-4020-0777-4. Retrieved 2 June 2013.
- Ramel, Gordon. "Lichen Reproductive Structures". Retrieved 22 August 2014.
- Murtagh GJ, Dyer PS, Crittenden PD (April 2000). "Sex and the single lichen". Nature 404 (6778): 564. doi:10.1038/35007142. PMID 10766229.
- Kirk et al., pp. 378–81.
- Form and structure - Sticta and Dendriscocaulon, Australian Botanic Garden website, 
- Lutzoni, F.; Kauff, F.; Cox, C. J.; McLaughlin, D.; Celio, G.; Dentinger, B.; Padamsee, M.; Hibbett, D.; et al. (2004). "Assembling the fungal tree of life: progress, classification, and evolution of subcellular traits". American Journal of Botany 91 (10): 1446–1480. doi:10.3732/ajb.91.10.1446. ISSN 0002-9122. PMID 21652303.
- Rikkinen J. (1995). "What's behind the pretty colors? A study on the photobiology of lichens". Bryobrothera 4: 1–226.
- Friedl T, Büdel B. "Photobionts". In Nash III TH. Lichen Biology. Cambridge: Cambridge University Press.
- "Alan Silverside's Lichen Glossary (a-f), Alan Silverside". Retrieved 10 October 2014.
- "Sciencemag.org". Retrieved 10 October 2014.
- O'Brien, H.; Miadlikowska, J.; Lutzoni, F. (2005). "Assessing host specialization in symbiotic cyanobacteria associated with four closely related species of the lichen fungus Peltigera". European Journal of Phycology 40: 363–378. doi:10.1080/09670260500342647.
- Guzow-Krzeminska, B (2006). "Photobiont ?exibility in thelichen Protoparmeliopsis muralis as revealed by ITS rDNA analyses". Lichenologist 38: 469–476. doi:10.1017/s0024282906005068.
- Ohmura, Y.; Kawachi, M.; Kasai, F.; Watanabe, M. "Genetic combinations of symbionts in a vegetatively reproducing lichen, Parmotrema tinctorum, based on ITS rDNA sequences" (2006)". Bryologist 109: 43–59. doi:10.1639/0007-2745(2006)109[0043:gcosia]2.0.co;2.
- Piercey-Normore (2006). "The lichen-forming asco-mycete Evernia mesomorpha associates with multiplegenotypes of Trebouxia jamesii". New Phytologist 169: 331–344. doi:10.1111/j.1469-8137.2005.01576.x.
- "Lichens: Fossil Record", University of California Museum of Paleontology, 
- Speer BR, Waggoner B. "Fossil Record of Lichens". University of California Museum of Paleontology. Retrieved 2010-02-16.
- Poinar Jr., GO. (1992). Life in Amber. Stanford University Press.
- Peterson EB. (2000). "An overlooked fossil lichen (Lobariaceae)". Lichenologist 32 (3): 298–300. doi:10.1006/lich.1999.0257.
- Taylor, T. N.; Hass, H.; Remy, W.; Kerp, H. (1995). "The oldest fossil lichen". Nature 378 (6554): 244–244. Bibcode:1995Natur.378..244T. doi:10.1038/378244a0.
- Taylor WA, Free CB, Helgemo R, Ochoada J. (2004). "SEM analysis of spongiophyton interpreted as a fossil lichen". International Journal of Plant Science 165 (5): 875–81. doi:10.1086/422129.
- Jahren, A.H.; Porter, S.; Kuglitsch, J.J. (2003). "Lichen metabolism identified in Early Devonian terrestrial organisms". Geology 31 (2): 99–102. Bibcode:2003Geo....31...99J. doi:10.1130/0091-7613(2003)031<0099:LMIIED>2.0.CO;2. ISSN 0091-7613.
- Fletcher, B. J.; Beerling, D. J.; Chaloner, W. G. (2004). "Stable carbon isotopes and the metabolism of the terrestrial Devonian organism Spongiophyton". Geobiology 2 (2): 107–119. doi:10.1111/j.1472-4677.2004.00026.x.
- Edwards D, Axe L. (2012). "Evidence for a fungal affinity for Nematasketum, a close ally of Prototaxites". Botanical Journal of the Linnaean Society 168: 1–18.
- Retallack G.J., and Landing, E. (2014). "Affinities and architecture of Devonian trunks of Prototaxites loganii". Mycologia 106: 1143–1156.
- Karatygin IV, Snigirevskaya NS, Vikulin SV., I. V.; Snigirevskaya, N. S.; Vikulin, S. V. (2009). "The most ancient terrestrial lichen Winfrenatia reticulata : A new find and new interpretation". Paleontological Journal 43 (1): 107–14. doi:10.1134/S0031030109010110.
- Karatygin IV, Snigirevskaya NS, Vikulin SV. (2007). "Two types of symbiosis with participation of Fungi from Early Devonian Ecosystems". XV Congress of European Mycologists, Saint Petersburg, Russia, September 16–21, 2007. 1 (1): 226.
- Schoch CL, Sung GH, López-Giráldez F, Townsend JP, Miadlikowska J, Hofstetter V, Robbertse B, Matheny PB, Kauff F, Wang Z, Gueidan C, Andrie RM, Trippe K, Ciufetti LM, Wynns A, Fraker E, Hodkinson BP, Bonito G, Groenewald JZ, Arzanlou M, de Hoog GS, Crous PW, Hewitt D, Pfister DH, Peterson K, Gryzenhout M, Wingfield MJ, Aptroot A, Suh SO, Blackwell M, Hillis DM, Griffith GW, Castlebury LA, Rossman AY, Lumbsch HT, Lücking R, Büdel B, Rauhut A, Diederich P, Ertz D, Geiser DM, Hosaka K, Inderbitzin P, Kohlmeyer J, Volkmann-Kohlmeyer B, Mostert L, O'Donnell K, Sipman H, Rogers JD, Shoemaker RA, Sugiyama J, Summerbell RC, Untereiner W, Johnston PR, Stenroos S, Zuccaro A, Dyer PS, Crittenden PD, Cole MS, Hansen K, Trappe JM, Yahr R, Lutzoni F, Spatafora JW (2009). "The Ascomycota tree of life: a phylum-wide phylogeny clarifies the origin and evolution of fundamental reproductive and ecological traits". Syst. Biol. 58 (2): 224–39. doi:10.1093/sysbio/syp020. PMID 20525580.
- Gargas A, DePriest PT, Grube M, Tehler A.; Depriest; Grube; Tehler (1995). "Multiple origins of lichen symbioses in fungi suggested by SSU rDNA phylogeny". Science 268 (5216): 1492–95. Bibcode:1995Sci...268.1492G. doi:10.1126/science.7770775. PMID 7770775.
- Honegger R. (1998). "The lichen symbiosis - what is so spectacular about it?". Lichenologist 30: 193–212. doi:10.1017/s002428299200015x.
- Wedin M, Döring H, Gilenstam G. (2004). "Saprotrophy and lichenization as options for the same fungl species on different substrata: environmental plasticity and fungal lifestyles in the Strictis-Conotrema complex". New Phytologist 16: 459–65. doi:10.1111/j.1469-8137.2004.01198.x.
- Taylor TN.; Hass, Hagen; Kerp, Hans (1997). "A cyanolichens from the Lower Devnian Rhynie chert". American Journal of Botany 84 (7): 992–1004. doi:10.2307/2446290. JSTOR 2446290. PMID 21708654.
- Yuan X, Xiao S, Taylor TN.; Xiao; Taylor (2005). "Lichen-like symbiosis 600 million years ago". Science 308 (5724): 1017–20. Bibcode:2005Sci...308.1017Y. doi:10.1126/science.1111347. PMID 15890881.
- Retallack G.J. (2015). "Acritarch evidence of a late Precambrian adaptive radiation of Fungi.". Botanica Pacifica 4(2): 19–33.
- Retallack GJ. (2007). "Growth, decay and burial compaction of Dickinsonia, an iconic Ediacaran fossil" (PDF). Alcheringa: an Australasian Journal of Palaeontology 31 (3): 215–240. doi:10.1080/03115510701484705. Retrieved 2008-02-04.
- Retallack GJ. (1994). "Were the Ediacaran Fossils Lichens?". Paleobiology 20 (4): 523–44. ISSN 0094-8373. JSTOR 2401233.
- Switek B (2012). "Controversial claim puts life on land 65 million years early". Nature. doi:10.1038/nature.2012.12017.
- Retallack, G.J., Dunn, K.L., and Saxby, J.year= 2015. "Problematic Mesoproterozoic fossil Horodyskia from Glacier National Park, Montana, USA.". Precambrian Research 226: 125–142.
- Retallack, G.J., Krull, E.S., Thackray, G.D., and Parkinson, D. (2013). "Problematic urn-shaped fossils from a Paleoproterozoic (2.2 Ga) paleosol in South Africa.". Precambrian Research 235: 71–87.
- Photo Gallery, Joshua Tree Lichens, National Park Service
- "Pollution, The Plant Underworld, Australian Botanic Gardens". Retrieved 10 October 2014.
- Nash, T.H. (1996). Lichen Biology. Cambridge, U.K.: Cambridge University Press.
- Dobson, F.S. (2011). Lichens, an illustrated guide to the British and Irish species. Slough, England: Richmond Publishing Co. Ltd. ISBN 9780855463151.
- Chen, Jie; Blume, Hans-Peter; Beyer, Lothar (1 September 1999). "Weathering of rocks induced by lichen colonization - a review" (PDF). Catena - An Interdisciplinary Journal of Soil Science (Elsevier) (Catena 39 2000 121–146): 124. Retrieved 21 March 2015.
- Chen, Jie; Blume, Hans-Peter; Beyer, Lothar (1 September 1999). "Weathering of rocks induced by lichen colonization - a review" (PDF). Catena - An Interdisciplinary Journal of Soil Science (Elsevier) (Catena 39 2000 121–146): 129. Retrieved 21 March 2015.
- "Fertilization of the desert soil by rock-eating snails", Clive G. Jones & Moshe Shachak, Nature 346, 839–841 (30 August 1990)
- Walker, T. R. (2007). "Lichens of the boreal forests of Labrador, Canada: A checklist". Evansia 24 (3): 85–90. doi:10.1639/0747-9859-24.3.85.
- Oksanen I., I (2006). "Ecological and biotechnological aspects of lichens". Applied Microbiology and Biotechnology 73 (4): 723–34. doi:10.1007/s00253-006-0611-3. PMID 17082931.
- Lawrey, James D. (1994). "Lichen Allelopathy: A Review". In Inderjit; K. M. M. Dakshini; Frank A. Einhellig. Allelopathy. Organisms, Processes, and Applications. American Chemical Society. pp. 26–38. doi:10.1021/bk-1995-0582.ch002.
- Nash TH. (2008). Lichen Biology (2nd ed.). Cambridge, UK: Cambridge University Press. pp. 299–314. ISBN 0-521-69216-4.
- Knops JMH, Nash TH. (1991). "Mineral cycling and epiphytic lichens: Implications at the ecosystem level". Lichenologist 23 (3): 309–21. doi:10.1017/S0024282991000452.
- Halonen P, Hyvarinen M, Kauppi M. (1993). "Emission related and repeated monitoring of element concentrations in the epiphytic lichen Hypogymnia physodes in a coastal area, western Finland". Annales Botanici Fennici 30: 251–61.
- Walker T. R., Pystina T. N. (2006). "The use lichens to monitor terrestrial pollution and ecological impacts caused by oil and gas industries in the Pechora Basin, NW Russia". Herzogia 19: 229–238.
- Walker T. R., Crittenden P. D., Young S. D., Prystina T. (2006). "An assessment of pollution impacts due to the oil and gas industries in the Pechora basin, north-eastern European Russia". Ecological Indicators 6 (2): 369–387. doi:10.1016/j.ecolind.2005.03.015.
- Walker T. R., Crittenden P. D., Young S. D.; Crittenden; Young (2003). "Regional variation in the chemical composition of winter snowpack and terricolous lichens in relation to sources of acid emissions in the Usa River Basin, northeastern European Russia". Environmental Pollution 125 (3): 401–412. doi:10.1016/s0269-7491(03)00080-0. PMID 12826418.
- Hogan, C. Michael (2010). "Abiotic factor". Encyclopedia of Earth. Washington, D.C.: National Council for Science and the Environment. Retrieved 27 October 2013.
- Beltman IH, de Kok LJ, Kuiper PJC, van Hasselt PR. (1980). "Fatty acid composition and chlorophyll content of epiphytic lichens and a possible relation to their sensitivity to air pollution". Oikos 35 (3): 321–26. doi:10.2307/3544647. JSTOR 3544647.
- Emmerich R, Giez I, Lange OL, Proksch P. (1993). "Toxicity and antifeedant activity of lichen compounds against the polyphagous herbivorous insect Spodoptera littoralis". Phytochemistry 33 (6): 1389–94. doi:10.1016/0031-9422(93)85097-B.
- Beschel RE (1950). "Flecten als altersmasstab Rezenter morainen". Zeitschrift für Gletscherkunde und Glazialgeologie 1: 152–161.
- Holocene climatic and glacial history of the central Sierra Nevada, California, R. R. Curry, pp. 1–47, 1969, Geological Society of America Special Paper, 123, S. A. Schumm and W. C. Bradley, eds., 1969
- Sowers, J. M., Noller, J. S., and Lettis, W. R., eds., 1997, Dating and Earthquakes: Review of Quaternary Geochronology and its Application to Paleoseismology. U.S. Nuclear Regulatory Commission, NUREG/CR 5562.
- John L. Innes. "Lichenometry". Progress in Physical Geography 9 (187).
- Francesca Cappitelli; Claudia Sorlini (2008). "Microorganisms Attack Synthetic Polymers in Items Representing Our Cultural Heritage". Applied and Environmental Microbiology 74: 564–569. doi:10.1128/AEM.01768-07. PMC 2227722. PMID 18065627.
- Geoffrey Michael Gadd (March 2010). "Metals, minerals and microbes: geomicrobiology and bioremediation". Microbiology 156 (Pt 3): 609–643. doi:10.1099/mic.0.037143-0. PMID 20019082.
- "Crottle". Dictionary of the Scots Language. Retrieved 10 May 2014.
- Casselman, Karen Leigh; Dean, Jenny (1999). Wild color: [the complete guide to making and using natural dyes]. New York: Watson-Guptill Publications. ISBN 0-8230-5727-5.
- Muller, K (2001). "Pharmaceutically Relevant Metabolites from Lichens". Applied Microbiology and Biotechnology 59: 9–10.
- Morton E. Winters, J. and Smith, L. (2010). "An Analysis of Antiseptic and Antibiotic Properties of Variously Treated Mosses and Lichens".
- McCleary, J. A.; Walkington, D.L. (1964). "Antimicrobial Activity of the Cactaceae". The Bulletin 91 (5): 361–369. doi:10.2307/2483428.
- Morton et al., 2010
- Bustinza, F. (1952). "Antibacterial Substances from Lichens". Economic Botany 6 (4): 402–406. doi:10.1007/bf02984888.
- "Themodelrailroader.com". Retrieved 10 October 2014.
- Johnson, Christopher; James P. Bennett; Steven M. Biro; Juan Camilo Duque-Velasquez; Cynthia M. Rodriguez; Richard A. Bessen; Tonie E. Rocke (17 May 2011). "Degradation of the Disease-Associated Prion Protein by a Serine Protease from Lichens". PLoS ONE 6 (5): e19836. Bibcode:2011PLoSO...6E9836J. doi:10.1371/journal.pone.0019836. PMC 3092769. PMID 21589935.
- Yam, Philip. "Natural Born Prion Killers: Lichens Degrade "Mad Cow" Related Brain Pathogen". Scientific American. Retrieved 20 May 2011.
- Honegger R. (2000). "Simon Schwender (1829–1919) and the dual hypothesis in lichens". Bryologist 103 (2): 307–13. doi:10.1639/0007-2745(2000)103[0307:SSATDH]2.0.CO;2. ISSN 0007-2745. JSTOR 3244159.
- Treub, Melchior (1873) Onderzoekingen over de natuur der lichenen. Dissertation Leiden University.
- This was scraped from a dry, concrete-paved section of a drainage ditch. This entire image covers a square that is approximately 1.7 millimeters on a side. The numbered ticks on the scale represent distances of 230 micrometers, or slightly less than 0.25 millimeter.
- Ahmadjian V. (1993). The Lichen Symbiosis. New York: John Wiley & Sons. ISBN 0-471-57885-1.
- Brodo, I. M., S. D. Sharnoff, and S. Sharnoff, 2001. Lichens of North America. Yale University Press, New Haven.
- Gilbert, O. 2004. The Lichen Hunters. The Book Guild Ltd. England.
- Haugan, Reidar; Timdal, Einar (1992). "Squamarina scopulorum (Lecanoraceae), a new lichen species from Norway". Nordic Journal of Botany 12 (3): 357–360. doi:10.1111/j.1756-1051.1992.tb01314.x.
- Hawksworth, D. L. and Seaward, M. R. D. 1977. Lichenology in the British Isles 1568–1975 The Richmond Publishing Co. Ltd., 1977.
- Kershaw, K. A. Physiological Ecology of Lichens, 1985. Cambridge University Press Cambridge.
- Kirk PM, Cannon PF, Minter DW, Stalpers JA. (2008). Dictionary of the Fungi. (10th ed.). Wallingford: CABI. ISBN 978-0-85199-826-8.
- Knowles M.C. (1929). "Lichens of Ireland". Proceedings of the Royal Irish Academy 38: 1–32.
- Purvis, O. W., Coppins, B. J., Hawksworth, D. L., James, P. W. and Moore, D. M. (editors) 1992. The Lichen Flora of Great Britain and Ireland. Natural History Museum, London.
- Sanders W.B. (2001). "Lichens: interface between mycology and plant morphology". BioScience 51 (12): 1025–1035. doi:10.1641/0006-3568(2001)051[1025:LTIBMA]2.0.CO;2.
- Seaward M. R. D. (1984). "Census Catalogue of Irish Lichens". Glasra 8: 1–32.
- Whelan, P. 2011. Lichens of Ireland. The Collins Press, Cork, Ireland.
|Wikimedia Commons has media related to Lichens.|
|Look up lichen in Wiktionary, the free dictionary.|
Identification and classification
- University of California Museum of Paleontology microscopic image of cross section of crustose or squamulose lichen
- Earth Life Web - Schematic drawings of internal lichen structures for various growth forms
- University of Sydney lichen biology
- Memorial University's NL Nature project, focusing primarily on lichens
- Fungi that discovered agriculture
- Lichens of Armenia
- Lichens of Ireland
- Lichens of North America
- Pacific Northwest Fungi Online Journal, includes articles on lichens
- Pictures of Tropical Lichens