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Symbiosis

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This article is about the biological phenomenon. For other uses, see Symbiosis (disambiguation).
In a cleaning symbiosis, the clownfish feeds on small invertebrates, that otherwise have potential to harm the sea anemone, and the fecal matter from the clownfish provides nutrients to the sea anemone. The clownfish is protected from predators by the anemone's stinging cells, to which the clownfish is immune. The relationship is therefore classified as mutualistic.[1]

Symbiosis (Ancient Greek συμβίωσις symbíōsis: living with, companionship < σύν sýn: together; and βίωσις bíōsis: living)[2] is any type of a close and long-term biological interaction, between two organisms of different species. The two organisms, termed symbionts, can be either in a mutualistic, a commensalistic, or a parasitic relationship.[3] In 1879, Heinrich Anton de Bary defined symbiosis as "the living together of unlike organisms".

The term is sometimes more exclusively used in a restricted, mutualistic sense, where both symbionts contribute to each other's subsistence.[3]

Symbiosis can be obligatory, which means that one, or both of the symbionts depend on each other for survival, or facultative (optional), when they can also subsist independently.

Symbiosis is also classified by physical attachment. Symbionts forming a single body live in conjunctive symbiosis, while all other arrangements are called disjunctive symbiosis.[4] When one organism lives on the surface of another, such as head lice on humans, it is called ectosymbiosis; when one partner lives inside the tissues of another, such as Symbiodinium within coral, it is termed endosymbiosis.[5][6]

Definition

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Diagram of the six possible types of symbiotic relationship, from mutual benefit to mutual harm.

The definition of symbiosis was a matter of debate for 130 years.[7] In 1877, Albert Bernhard Frank used the term symbiosis to describe the mutualistic relationship in lichens.[8][9] In 1878, the German mycologist Heinrich Anton de Bary defined it as "the living together of unlike organisms".[10][11][12] The definition has varied among scientists, with some advocating that it should only refer to persistent mutualisms, while others thought it should apply to all persistent biological interactions (in other words, to mutualism, commensalism, and parasitism, but excluding brief interactions such as predation). In the 21st century, the latter has become the definition widely accepted by biologists.[13]

In 1949, Edward Haskell proposed an integrative approach with a classification of "co-actions",[14] later adopted by biologists as "interactions".[15][16][17][18]

Types

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Obligate versus facultative

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Relationships can be obligate, meaning that one or both of the symbionts entirely depend on each other for survival. For example, in lichens, which consist of fungal and photosynthetic symbionts, the fungal partners cannot live on their own.[11][19][20][21] The algal or cyanobacterial symbionts in lichens, such as Trentepohlia, can generally live independently, and their part of the relationship is therefore described as facultative (optional), or non-obligate.[22] When one of the participants in a symbiotic relationship is capable of photosynthesis, as with lichens, it is called photosymbiosis.[23][24]

Ectosymbiosis versus endosymbiosis

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Alder tree root nodule houses endosymbiotic nitrogen-fixing bacteria.
Main article: Ectosymbiosis
Further information: Endosymbiont

Ectosymbiosis is any symbiotic relationship in which the symbiont lives on the body surface of the host, including the inner surface of the digestive tract or the ducts of exocrine glands.[6][25] Examples of this include ectoparasites such as lice; commensal ectosymbionts such as the barnacles, which attach themselves to the jaw of baleen whales; and mutualist ectosymbionts such as cleaner fish.

Contrastingly, endosymbiosis is any symbiotic relationship in which one symbiont lives within the tissues of the other, either within the cells or extracellularly.[6][26] Examples include diverse microbiomes: rhizobia, nitrogen-fixing bacteria that live in root nodules on legume roots; actinomycetes, nitrogen-fixing bacteria such as Frankia, which live in alder root nodules; single-celled algae inside reef-building corals; and bacterial endosymbionts that provide essential nutrients to about 10%–15% of insects.[27]

In endosymbiosis, the host cell lacks some of the nutrients which the endosymbiont provides. As a result, the host favors endosymbiont's growth processes within itself by producing some specialized cells. These cells affect the genetic composition of the host in order to regulate the increasing population of the endosymbionts and ensure that these genetic changes are passed onto the offspring via vertical transmission (heredity).[28]

As the endosymbiont adapts to the host's lifestyle, the endosymbiont changes dramatically. There is a drastic reduction in its genome size, as many genes are lost during the process of metabolism, and DNA repair and recombination, while important genes participating in the DNA-to-RNA transcription, protein translation and DNA/RNA replication are retained. The decrease in genome size is due to loss of protein coding genes and not due to lessening of inter-genic regions or open reading frame (ORF) size. Species that are naturally evolving and contain reduced sizes of genes can be accounted for an increased number of noticeable differences between them, thereby leading to changes in their evolutionary rates. When endosymbiotic bacteria related with insects are passed on to the offspring strictly via vertical genetic transmission, intracellular bacteria go across many hurdles during the process, resulting in the decrease in effective population sizes, as compared to the free-living bacteria. The incapability of the endosymbiotic bacteria to reinstate their wild type phenotype via a recombination process is called Muller's ratchet phenomenon. Muller's ratchet phenomenon, together with less effective population sizes, leads to an accretion of deleterious mutations in the non-essential genes of the intracellular bacteria.[29] This can be due to lack of selection mechanisms prevailing in the relatively "rich" host environment.[30][31]

Competition

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Main article: Competition (biology)

Competition can be defined as an interaction between organisms or species, in which the fitness of one is lowered by the presence of another.[32] Limited supply of at least one resource (such as food, water, and territory) used by both usually facilitates this type of interaction, although the competition can also be for other resources.[33]

Amensalism

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The black walnut secretes a chemical from its roots that harms neighboring plants, an example of antagonism.

Amensalism is a non-symbiotic, asymmetric interaction where one species is harmed or killed by the other, and one is unaffected by the other.[34][35] There are two types of amensalism, competition and antagonism (or antibiosis). Competition is where a larger or stronger organism deprives a smaller or weaker one of a resource. Antagonism occurs when one organism is damaged or killed by another through a chemical secretion. An example of competition is a sapling growing under the shadow of a mature tree. The mature tree can rob the sapling of necessary sunlight and, if the mature tree is very large, it can take up rainwater and deplete soil nutrients. Throughout the process, the mature tree is unaffected by the sapling. Indeed, if the sapling dies, the mature tree gains nutrients from the decaying sapling. An example of antagonism is Juglans nigra (black walnut), secreting juglone, a substance which destroys many herbaceous plants within its root zone.[36]

The term amensalism is often used to describe strongly asymmetrical competitive interactions, such as between the Spanish ibex and weevils of the genus Timarcha which feed upon the same type of shrub. Whilst the presence of the weevil has almost no influence on food availability, the presence of ibex has an enormous detrimental effect on weevil numbers, as they consume significant quantities of plant matter and incidentally ingest the weevils upon it.[37]

Commensalism

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Main article: Commensalism
Commensal mites travelling (phoresy) on a fly (Pseudolynchia canariensis)

Commensalism describes a relationship between two living organisms where one benefits and the other is not significantly harmed or helped. It is derived from the English word commensal, used of human social interaction. It derives from a medieval Latin word meaning sharing food, formed from com- (with) and mensa (table).[38][39]

Commensal relationships may involve one organism using another for transportation (phoresy) or for housing (inquilinism), or it may also involve one organism using something another created, after its death (metabiosis). Examples of metabiosis are hermit crabs using gastropod shells to protect their bodies, and spiders building their webs on plants.

Mutualism

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Main article: Mutualism (biology)
Hermit crab, Calcinus laevimanus, with sea anemone

Mutualism or interspecies reciprocal altruism is a long-term relationship between individuals of different species where both individuals benefit.[38] Mutualistic relationships may be either obligate for both species, obligate for one but facultative for the other, or facultative for both.

Bryoliths document a mutualistic symbiosis between a hermit crab and encrusting bryozoans.

Many herbivores have mutualistic gut flora to help them digest plant matter, which is more difficult to digest than animal prey.[5] This gut flora comprises cellulose-digesting protozoans or bacteria living in the herbivores' intestines.[40] Coral reefs result from mutualism between coral organisms and various algae living inside them.[41] Most land plants and land ecosystems rely on mutualism between the plants, which fix carbon from the air, and mycorrhyzal fungi, which help in extracting water and minerals from the ground.[42]

An example of mutualism is the relationship between the ocellaris clownfish that dwell among the tentacles of Ritteri sea anemones. The territorial fish protects the anemone from anemone-eating fish, and in turn, the anemone stinging tentacles protect the clownfish from its predators. A special mucus on the clownfish protects it from the stinging tentacles.[43]

A further example is the goby, a fish which sometimes lives together with a shrimp. The shrimp digs and cleans up a burrow in the sand in which both the shrimp and the goby fish live. The shrimp is almost blind, leaving it vulnerable to predators when outside its burrow. In case of danger, the goby touches the shrimp with its tail to warn it. When that happens both the shrimp and goby quickly retreat into the burrow.[44] Different species of gobies (Elacatinus spp.) also clean up ectoparasites in other fish, possibly another kind of mutualism.[45]

A spectacular example of obligate mutualism is the relationship between the siboglinid tube worms and symbiotic bacteria that live at hydrothermal vents and cold seeps. The worm has no digestive tract and is wholly reliant on its internal symbionts for nutrition. The bacteria oxidize either hydrogen sulfide or methane, which the host supplies to them. These worms were discovered in the late 1980s at the hydrothermal vents near the Galapagos Islands and have since been found at deep-sea hydrothermal vents and cold seeps in all of the world's oceans.[46]

Mutualism improves both organism's competitive ability and will outcompete organisms of the same species that lack the symbiont.[47]

A facultative symbiosis is seen in encrusting bryozoans and hermit crabs. The bryozoan colony (Acanthodesia commensale) develops a cirumrotatory growth and offers the crab (Pseudopagurus granulimanus) a helicospiral-tubular extension of its living chamber that initially was situated within a gastropod shell.[48]

Parasitism

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Main article: Parasitism
Head (scolex) of tapeworm Taenia solium is adapted to parasitism with hooks and suckers to attach to its host.

In a parasitic relationship, the parasite benefits while the host is harmed.[49] Parasitism takes many forms, from endoparasites that live within the host's body to ectoparasites and parasitic castrators that live on its surface and micropredators like mosquitoes that visit intermittently. Parasitism is an extremely successful mode of life; about 40% of all animal species are parasites, and the average mammal species is host to 4 nematodes, 2 cestodes, and 2 trematodes.[50]

Mimicry

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Main article: Mimicry

Mimicry is a form of symbiosis in which a species adopts distinct characteristics of another species to alter its relationship dynamic with the species being mimicked, to its own advantage. Among the many types of mimicry are Batesian and Müllerian, the first involving one-sided exploitation, the second providing mutual benefit. Batesian mimicry is an exploitative three-party interaction where one species, the mimic, has evolved to mimic another, the model, to deceive a third, the dupe. In terms of signalling theory, the mimic and model have evolved to send a signal; the dupe has evolved to receive it from the model. This is to the advantage of the mimic but to the detriment of both the model, whose protective signals are effectively weakened, and of the dupe, which is deprived of an edible prey. For example, a wasp is a strongly-defended model, which signals with its conspicuous black and yellow coloration that it is an unprofitable prey to predators such as birds which hunt by sight; many hoverflies are Batesian mimics of wasps, and any bird that avoids these hoverflies is a dupe.[51][52] In contrast, Müllerian mimicry is mutually beneficial as all participants are both models and mimics.[53][54] For example, different species of bumblebee mimic each other, with similar warning coloration in combinations of black, white, red, and yellow, and all of them benefit from the relationship. [55]

Cleaning symbiosis

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Main article: Cleaning symbiosis

Cleaning symbiosis is an association between individuals of two species, where one (the cleaner) removes and eats parasites and other materials from the surface of the other (the client).[56] It is putatively mutually beneficial, but biologists have long debated whether it is mutual selfishness, or simply exploitative. Cleaning symbiosis is well known among marine fish, where some small species of cleaner fish – notably wrasses, but also species in other genera – are specialized to feed almost exclusively by cleaning larger fish and other marine animals.[57] In a supreme situation, the host species (fish or marine life) will display itself at a designated station deemed the "cleaning station".[58]

Cleaner fish play an essential role in the reduction of parasitism on marine animals. Some shark species participate in cleaning symbiosis, where cleaner fish remove ectoparasites from the body of the shark.[59] A study by Raymond Keyes addresses the atypical behavior of a few shark species when exposed to cleaner fish. In this experiment, cleaner wrasse (Labroides dimidiatus) and various shark species were placed in a tank together and observed. The different shark species exhibited different responses and behaviors around the wrasse. For example, Atlantic and Pacific lemon sharks consistently react to the wrasse fish in a fascinating way. During the interaction, the shark remains passive and the wrasse swims to it. It begins to scan the shark's body, sometimes stopping to inspect specific areas. Commonly, the wrasse would inspect the gills, labial regions, and skin. When the wrasse makes its way to the mouth of the shark, the shark often ceases breathing for up to two and a half minutes so that the fish is able to scan the mouth. Then, the fish passes further into the mouth to examine the gills, specifically the buccopharyngeal area, which typically holds the most parasites. When the shark begins to close its mouth, the wrasse finishes its examination and goes elsewhere. Male bull sharks exhibit slightly different behavior at cleaning stations: as the shark swims into a colony of wrasse fish, it drastically slows its speed to allow the cleaners to do their job. After approximately one minute, the shark returns to normal swimming speed.[59]

Role in evolution

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Leafhoppers protected by meat ants
Further information: Co-evolution

Symbiosis is increasingly recognized as an important selective force behind evolution;[5][60] many species have a long history of interdependent co-evolution.[61]

Although symbiosis was once discounted as an anecdotal evolutionary phenomenon, evidence is now overwhelming that obligate or facultative associations among microorganisms and between microorganisms and multicellular hosts had crucial consequences in many landmark events in evolution and in the generation of phenotypic diversity and complex phenotypes able to colonise new environments.[62]

Hologenome development and evolution

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Evolution originated from changes in development where variations within species are selected for or against because of the symbionts involved.[63] The hologenome theory relates to the holobiont and symbionts genome together as a whole.[64] Microbes live everywhere in and on every multicellular organism.[65] Many organisms rely on their symbionts in order to develop properly, this is known as co-development. In cases of co-development the symbionts send signals to their host which determine developmental processes. Co-development is commonly seen in both arthropods and vertebrates.[63]

Symbiogenesis

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Main article: Symbiogenesis

One hypothesis for the origin of the nucleus in eukaryotes (plants, animals, fungi, and protists) is that it developed from a symbiogenesis between bacteria and archaea.[5][66][67] It is hypothesized that the symbiosis originated when ancient archaea, similar to modern methanogenic archaea, invaded and lived within bacteria similar to modern myxobacteria, eventually forming the early nucleus. This theory is analogous to the accepted theory for the origin of eukaryotic mitochondria and chloroplasts, which are thought to have developed from a similar endosymbiotic relationship between proto-eukaryotes and aerobic bacteria.[68] Evidence for this includes the fact that mitochondria and chloroplasts divide independently of the cell, and that these organelles have their own genome.[69]

The biologist Lynn Margulis, famous for her work on endosymbiosis, contended that symbiosis is a major driving force behind evolution. She considered Darwin's notion of evolution, driven by competition, to be incomplete and claimed that evolution is strongly based on co-operation, interaction, and mutual dependence among organisms. According to Margulis and her son Dorion Sagan, "Life did not take over the globe by combat, but by networking."[70]

Major examples of co-evolutionary relationships

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Mycorrhiza

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About 80% of vascular plants worldwide form symbiotic relationships with fungi, in particular in arbuscular mycorrhizas.[71]

Pollination is a mutualism between flowering plants and their animal pollinators.

Pollination

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A fig is pollinated by the fig wasp, Blastophaga psenes.
Further information: Entomophily, Ornithophily, and Reproductive coevolution in Ficus

Flowering plants and the animals that pollinate them have co-evolved. Many plants that are pollinated by insects (in entomophily), bats, or birds (in ornithophily) have highly specialized flowers modified to promote pollination by a specific pollinator that is correspondingly adapted. The first flowering plants in the fossil record had relatively simple flowers. Adaptive speciation quickly gave rise to many diverse groups of plants, and, at the same time, corresponding speciation occurred in certain insect groups. Some groups of plants developed nectar and large sticky pollen, while insects evolved more specialized morphologies to access and collect these rich food sources. In some taxa of plants and insects, the relationship has become dependent,[72] where the plant species can only be pollinated by one species of insect.[73]

Pseudomyrmex ant on bull thorn acacia (Vachellia cornigera) with Beltian bodies that provide the ants with protein[74]

Acacia ants and acacias

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Main article: Pseudomyrmex ferruginea

The acacia ant (Pseudomyrmex ferruginea) is an obligate plant ant that protects at least five species of "Acacia" (Vachellia)[a] from preying insects and from other plants competing for sunlight, and the tree provides nourishment and shelter for the ant and its larvae.[74][75]

Seed dispersal

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Main article: Seed dispersal syndrome

Seed dispersal is the movement, spread or transport of seeds away from the parent plant. Plants have limited mobility and rely upon a variety of dispersal vectors to transport their propagules, including both abiotic vectors such as the wind and living (biotic) vectors like birds. In order to attract animals, these plants evolved a set of morphological characters such as fruit colour, mass, and persistence correlated to particular seed dispersal agents.[76] For example, plants may evolve conspicuous fruit colours to attract avian frugivores, and birds may learn to associate such colours with a food resource.[77]

Rhizobia

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Main article: Rhizobia

Lichens

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Main article: Lichen

See also

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Notes

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  1. ^ The acacia ant protects at least 5 species of "Acacia", now all renamed to Vachellia: V. chiapensis, V. collinsii, V. cornigera, V. hindsii and V. sphaerocephala.

References

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  1. ^ Miller, Allie. "Intricate Relationship Allows the Other to Flourish: the Sea Anemone and the Clownfish". AskNature. The Biomimicry Institute. Retrieved 15 February 2015.
  2. ^ συμβίωσις, σύν, βίωσις. Liddell, Henry George; Scott, Robert; A Greek–English Lexicon at the Perseus Project
  3. ^ a b "symbiosis". Oxford English Dictionary (Online ed.). Oxford University Press. (Subscription or participating institution membership required.)
  4. ^ "Symbiosis". Dorland's Illustrated Medical Dictionary. Philadelphia: Elsevier Health Sciences, 2007. Credo Reference. Web. 17 September 2012
  5. ^ a b c d Moran 2006
  6. ^ a b c Paracer & Ahmadjian 2000, p. 12
  7. ^ Martin, Bradford D.; Schwab, Ernest (2012), "Symbiosis: 'Living together' in chaos", Studies in the History of Biology, 4 (4): 7–25
  8. ^ Frank, A.B. (1877). "Über die biologischen Verkältnisse des Thallus einiger Krustflechten" [On the biological relationships of the thallus of some crustose lichens]. Beiträge zur Biologie der Pflanzen (in German). 2: 123–200. From p. 195: "Nach den erweiterten Kenntnissen, die wir in den letzten Jahren über das Zusammenleben zweier verschiedenartiger Wesen gewonnen haben, ist es ein dringendes Bedürfniss, die einzelnen von einander abweichenden Formen dieser Verhältnisse mit besonderen Bezeichnungen to belegen, da man fast für alle bisher den Ausdruck Parasitsmus gebrauchte. Wir müssen sämmtliche Fälle, wo überhaupt ein Auf- oder Ineinanderwohnen zweier verschiedener Species stattfindet, unter einen weitesten Begriff bringen, welcher die Rolle, die beide Wesen dabei spielen, noch nicht berücksichtigt, also auf das blosse Zusammenleben begründet ist, und wofür sich die Bezeichnung Symbiotismus empfehlen dürfte." (In the aftermath of the expanded knowledge that we have acquired in recent years about the coexistence of two distinct living things, there is an urgent need to bestow specific designations on the different individual forms of these relationships, since up till now one has used for almost all [of them] the term "parasitism". We must bring all cases, wherever one of two different species lives on or in the other, under the broadest concept which does not consider the roles that the two living things play thereby ([and] thus is based on mere coexistence) and for which the designation symbiotismus [i.e., symbiosis] might be suggested.)
  9. ^ "symbiosis". Oxford English Dictionary (Online ed.). Oxford University Press. (Subscription or participating institution membership required.)
  10. ^ de Bary, Heinrich Anton (14 September 1878). "Ueber Symbiose" [On Symbiosis]. Tageblatt für die Versammlung deutscher Naturforscher und Aerzte (in Cassel) [Daily Journal for the Conference of German Scientists and Physicians] (in German). 51: 121–126. From p. 121: " ... des Zusammenlebens ungleichnamiger Organismen, der Symbiose, ... " ( ... of the living together of unlike organisms, symbiosis, ... )
  11. ^ a b Wilkinson, David M. (August 2001). "At cross purposes". Nature. 412 (6846): 485. doi:10.1038/35087676. PMID 11484028. S2CID 5231135.
  12. ^ Douglas 1994, p. 1
  13. ^ Douglas 2010, pp. 5–12
  14. ^ Haskell, E. F. (1949). A clarification of social science. Main Currents in Modern Thought 7: 45–51.
  15. ^ Burkholder, P.R. (1952). "Cooperation and Conflict among Primitive Organisms". American Scientist. 40 (4): 601–631. JSTOR 27826458.
  16. ^ Bronstein, J.L. (2015). "The study of mutualism.". In Bronstein, J.L. (ed.). Mutualism. Oxford: Oxford University Press. ISBN 978-0-19-967565-4.
  17. ^ Pringle, Elizabeth G. (October 2016). "Orienting the Interaction Compass: Resource Availability as a Major Driver of Context Dependence". PLOS Biology. 14 (10): e2000891. doi:10.1371/journal.pbio.2000891. PMC 5061325. PMID 27732591.
  18. ^ Wootton, J.T.; Emmerson, M. (2005). "Measurement of Interaction Strength in Nature". Annual Review of Ecology, Evolution, and Systematics. 36: 419–44. doi:10.1146/annurev.ecolsys.36.091704.175535. JSTOR 30033811.
  19. ^ Isaac 1992, p. 266
  20. ^ Saffo 1993
  21. ^ Douglas 2010, p. 4
  22. ^ Muggia, Lucia; Vancurova, Lucie; Škaloud, Pavel; Peksa, Ondrej; Wedin, Mats; Grube, Martin (August 2013). "The symbiotic playground of lichen thalli--a highly flexible photobiont association in rock-inhabiting lichens". FEMS Microbiology Ecology. 85 (2): 313–323. Bibcode:2013FEMME..85..313M. doi:10.1111/1574-6941.12120. PMID 23530593.
  23. ^ "photosymbiosis". Oxford Reference.
  24. ^ Gault, Jordan A.; Bentlage, Bastian; Huang, Danwei; Kerr, Alexander M. (2021). "Lineage-specific variation in the evolutionary stability of coral photosymbiosis". Science Advances. 7 (39): eabh4243. Bibcode:2021SciA....7.4243G. doi:10.1126/sciadv.abh4243. PMC 8457658. PMID 34550731.
  25. ^ Nardon & Charles 2002
  26. ^ Sapp 1994, p. 142
  27. ^ Mus, Florence; Crook, Matthew B.; Garcia, Kevin; Garcia Costas, Amaya; Geddes, Barney A.; Kouri, Evangelia D.; Paramasivan, Ponraj; Ryu, Min-Hyung; Oldroyd, Giles E. D.; Poole, Philip S.; Udvardi, Michael K.; Voigt, Christopher A.; Ané, Jean-Michel; Peters, John W. (1 July 2016). Kelly, R. M. (ed.). "Symbiotic Nitrogen Fixation and the Challenges to Its Extension to Nonlegumes". Applied and Environmental Microbiology. 82 (13): 3698–3710. Bibcode:2016ApEnM..82.3698M. doi:10.1128/AEM.01055-16. ISSN 0099-2240. PMC 4907175. PMID 27084023.
  28. ^ Latorre, A.; Durban, A.; Moya, A.; Pereto, J. (2011). The role of symbiosis in eukaryotic evolution. Origins and evolution of life – An astrobiological perspective. pp. 326–339.
  29. ^ Moran, N. A. (April 1996). "Accelerated evolution and Muller's rachet in endosymbiotic bacteria". Proceedings of the National Academy of Sciences of the United States of America. 93 (7): 2873–2878. Bibcode:1996PNAS...93.2873M. doi:10.1073/pnas.93.7.2873. PMC 39726. PMID 8610134.
  30. ^ Andersson, Siv G.E; Kurland, Charles G. (July 1998). "Reductive evolution of resident genomes". Trends in Microbiology. 6 (7): 263–268. doi:10.1016/S0966-842X(98)01312-2. PMID 9717214.
  31. ^ Wernegreen, J.J. (November 2002). "Genome evolution in bacterial endosymbionts of insects". Nature Reviews. Genetics. 3 (11): 850–861. doi:10.1038/nrg931. PMID 12415315. S2CID 29136336.
  32. ^ "Species Interactions and Competition". Nature. Retrieved 5 February 2023.
  33. ^ Begon, M.; Harper, J.L.; Townsend, C.R. 1996. Ecology: individuals, populations, and communities, Third Edition. Blackwell, Cambridge, Massachusetts. Chapters 5 "Intraspecific Competition" and 8 "Interspecific Competition"
  34. ^ Toepfer, G. "Amensalism". In: BioConcepts. link Archived 2017-12-09 at the Wayback Machine.
  35. ^ Willey, Joanne M.; Sherwood, Linda M.; Woolverton, Cristopher J. (2013). Prescott's Microbiology (9th ed.). pp. 713–738. ISBN 978-0-07-751066-4.
  36. ^ Encyclopædia Britannica. "Amensalism (biology)". Retrieved September 30, 2014.
  37. ^ Gómez, José M.; González-Megías, Adela (2002). "Asymmetrical interactions between ungulates and phytophagous insects: Being different matters". Ecology. 83 (1): 203–11. doi:10.1890/0012-9658(2002)083[0203:AIBUAP]2.0.CO;2.
  38. ^ a b Paracer & Ahmadjian 2000, p. 6
  39. ^ Nair 2005
  40. ^ "symbiosis." The Columbia Encyclopedia. New York: Columbia University Press, 2008. Credo Reference. Web. 17 September 2012.
  41. ^ Toller, Rowan & Knowlton 2001
  42. ^ Harrison 2005
  43. ^ Lee 2003
  44. ^ Facey, Helfman & Collette 1997
  45. ^ Soares, M.C.; Côté, I.M>; Cardoso, S.C.; Bshary, R. (August 2008). "The cleaning goby mutualism: a system without punishment, partner switching or tactile stimulation" (PDF). Journal of Zoology. 276 (3): 306–312. doi:10.1111/j.1469-7998.2008.00489.x. Archived (PDF) from the original on 2022-10-09.
  46. ^ Cordes et al. 2005
  47. ^ Clay; Holah (1999). "Fungal endophyte symbiosis and plant diversity in successional fields". Science. 285 (5434): 1742–1744. doi:10.1126/science.285.5434.1742. PMID 10481011.
  48. ^ Klicpera, A.; Taylor, P.D.; Westphal, H. (1 Dec 2013). "Bryoliths constructed by bryozoans in symbiotic associations with hermit crabs in a tropical heterozoan carbonate system, Golfe d'Arguin, Mauritania". Marine Biodiversity. 43 (4): 429–444. Bibcode:2013MarBd..43..429K. doi:10.1007/s12526-013-0173-4. ISSN 1867-1616. S2CID 15841444.
  49. ^ Paracer & Ahmadjian 2000, p. 7
  50. ^ Dobson, Andy; Lafferty, Kevin D.; Kuris, Armand M.; Hechinger, Ryan F.; Jetz, Walter; National Research Council (2008). "Homage to Linnaeus: How Many Parasites? How Many Hosts?". In Avise, J.C.; Hubbell, S.P.; Ayala, F.J. (eds.). In the Light of Evolution: Volume II: Biodiversity and Extinction. Washington (DC): National Academies Press. p. 4. Archived from the original on Mar 22, 2023.
  51. ^ Vane-Wright, R. I. (1976). "A unified classification of mimetic resemblances". Biological Journal of the Linnean Society. 8: 25–56. doi:10.1111/j.1095-8312.1976.tb00240.x.
  52. ^ Bates, Henry Walter (1861). "Contributions to an insect fauna of the Amazon valley. Lepidoptera: Heliconidae". Transactions of the Linnean Society. 23 (3): 495–566. doi:10.1111/j.1096-3642.1860.tb00146.x.; Reprint: Bates, Henry Walter (1981). "Contributions to an insect fauna of the Amazon valley (Lepidoptera: Heliconidae)". Biological Journal of the Linnean Society. 16 (1): 41–54. doi:10.1111/j.1095-8312.1981.tb01842.x.
  53. ^ Müller, Fritz (1878). "Ueber die Vortheile der Mimicry bei Schmetterlingen". Zoologischer Anzeiger. 1: 54–55.
  54. ^ Müller, Fritz (1879). "Ituna and Thyridia; a remarkable case of mimicry in butterflies. (R. Meldola translation)". Proclamations of the Entomological Society of London. 1879: 20–29.
  55. ^ Mallet, James (2001). "Causes and consequences of a lack of coevolution in Mullerian mimicry". Evolutionary Ecology. 13 (7–8): 777–806. CiteSeerX 10.1.1.508.2755. doi:10.1023/a:1011060330515. S2CID 40597409.
  56. ^ Losey, G.S. (1972). "The Ecological Importance of Cleaning Symbiosis". Copeia. 1972 (4): 820–833. doi:10.2307/1442741. JSTOR 1442741.
  57. ^ Poulin, Robert; Grutter, A. S. (1996). "Cleaning symbiosis: proximate and adaptive explanations" (PDF). BioScience. 46 (7): 512–517. doi:10.2307/1312929. JSTOR 1312929. Archived (PDF) from the original on 2004-10-12.
  58. ^ Losey, George S. (1972). "The Ecological Importance of Cleaning Symbiosis". Copeia. 1972 (4): 820–833. doi:10.2307/1442741. ISSN 0045-8511. JSTOR 1442741.
  59. ^ a b Keyes, Raymond S. (1982). "Sharks: An Unusual Example of Cleaning Symbiosis". Copeia. 1982 (1): 225–227. doi:10.2307/1444305. ISSN 0045-8511. JSTOR 1444305.
  60. ^ Wernegreen 2004
  61. ^ Paracer & Ahmadjian 2000, pp. 3–4
  62. ^ Mutalipassi, Mirko; Riccio, Gennaro; Mazzella, Valerio; et al. (April 2021). "Symbioses of Cyanobacteria in Marine Environments: Ecological Insights and Biotechnological Perspectives". Marine Drugs. 19 (4). MDPI AG: 227. doi:10.3390/md19040227. PMC 8074062. PMID 33923826. Material was copied from this source, which is available under a Creative Commons Attribution 4.0 International License.
  63. ^ a b Li, Ci-Xiu; Shi, Mang; Tian, Jun-Hua; et al. (January 2015). "Unprecedented genomic diversity of RNA viruses in arthropods reveals the ancestry of negative-sense RNA viruses". eLife. 4. doi:10.7554/eLife.05378. PMC 4384744. PMID 25633976.
  64. ^ Rosenberg, E.; Zilber-Rosenberg, I. (March 2011). "Symbiosis and development: the hologenome concept". Birth Defects Research. Part C, Embryo Today. 93 (1): 56–66. doi:10.1002/bdrc.20196. PMID 21425442.
  65. ^ Morris, J.J. (2018-10-19). "What is the hologenome concept of evolution?". F1000Research. 7: 1664. doi:10.12688/f1000research.14385.1. PMC 6198262. PMID 30410727.
  66. ^ Brinkman et al. 2002
  67. ^ Golding & Gupta 1995
  68. ^ Margulis, Lynn (1981). Symbiosis in Cell Evolution. San Francisco: W. H. Freeman and Company. pp. 206–227. ISBN 978-0-7167-1256-5.
  69. ^ "Symbiosis". Bloomsbury Guide to Human Thought. London: Bloomsbury Publishing, 1993. Credo Reference. Web. 17 September 2012.
  70. ^ Sagan & Margulis 1986
  71. ^ Schüßler, A.; et al. (2001). "A new fungal phylum, the Glomeromycota: phylogeny and evolution". Mycol. Res. 105 (12): 1413–1421. doi:10.1017/S0953756201005196.
  72. ^ Harrison 2002
  73. ^ Danforth & Ascher 1997
  74. ^ a b Hölldobler, Bert; Wilson, Edward O. (1990). The Ants. Harvard University Press. pp. 532–533. ISBN 978-0-674-04075-5.
  75. ^ National Geographic. "Acacia Ant Video". Archived from the original on 2007-11-07.
  76. ^ Tamboia, Teri; Cipollini, Martin L.; Levey, Douglas J. (September 1996). "An evaluation of vertebrate seed dispersal syndromes in four species of black nightshade (Solanum sect. Solanum)". Oecologia. 107 (4): 522–532. Bibcode:1996Oecol.107..522T. doi:10.1007/bf00333944. PMID 28307396. S2CID 21341759.
  77. ^ Lim, Ganges; Burns, Kevin C. (2021-11-24). "Do fruit reflectance properties affect avian frugivory in New Zealand?". New Zealand Journal of Botany. 60 (3): 319–329. doi:10.1080/0028825X.2021.2001664. ISSN 0028-825X. S2CID 244683146.

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