Myrmecophyte

Myrmecophytes (/mərˈmɛkəfaɪt/; literally "ant-plant") are plants that live in a mutualistic association with a colony of ants. There are over 100 different genera of myrmecophytes.[1] These plants possess structural adaptations that provide ants with food and/or shelter. These specialized structures include domatia, food bodies, and extrafloral nectaries.[1] In exchange for food and shelter, ants aid the myrmecophyte in pollination, seed dispersal, gathering of essential nutrients, and/or defense.[1] Specifically, domatia adapted to ants may be called myrmecodomatia.[2]

Acacia ants

Mutualism

Myrmecophytes share a mutualistic relationship with ants, benefiting both the plants and ants. This association may be either facultative or obligate.[3]

Obligate mutualism

In obligate mutualisms, both of the organisms involved are interdependent; they cannot survive on their own. An example of this type of mutualism can be found in the plant genus Macaranga. All species of this genus provide food for ants in various forms, but only the obligate species produce domatia.[1] Some of the most common species of myrmecophytic Macaranga interact with ants in the genus Crematogaster. C. borneensis have been found to be completely dependent on its partner plant, not being able to survive without the provided nesting spaces and food bodies. In laboratory tests, the worker ants did not survive away from the plants, and in their natural habitat they were never found anywhere else.[4]

Facultative mutualism

Facultative mutualism is a type of relationship where the survival of both parties (plant and ants, in this instance) is not dependent upon the interaction. Both organisms can survive without the other species. Facultative mutualisms most often occur in plants that have extrafloral nectaries but no other specialized structures for the ants.[3] These non-exclusive nectaries allow a variety of animal species to interact with the plant.[3] Facultative relationships can also develop between non-native plant and ant species, where co-evolution has not occurred. For example, Old World legumes that were introduced to North America can be protected by ants that originated from a different region.[3]

Structural adaptations of myrmecophytes
Tuber on Myrmecodia tuberosa.

Domatia

Domatia are internal plant structures that appear to be specifically adapted for habitation by ants.[5] These cavities are found primarily in the stems, leaves, and spines of plants. Many different genera of plants offer domatia. Plants of the genus Acacia have some of the most widely recognized forms of domatia and offer some of the best examples of ant-plant obligate mutualism.[5] Different Acacia species provide a variety of resources needed for their codependent counterparts. One of these resources is the need for shelter. Acacia have enlarged thorns on their stems that are excavated by ants for use as housing structures.[5] Since the tree contains their nest, these aggressive ants react strongly to any disturbance of the tree, providing the myrmecophyte with defense from grazing herbivores and encroaching vines.[5]

Domatia can also be found within the tubers of certain plants.[6] Tubers form when the hypocotyls of a seedling swells to form a hollow, chambered structure that can become inhabited by ants.[6] The plant family Rubiaceae contains the most commonly known tuberous myrmecophyte, Myrmecodia.[6]

Enlarged thorns and beltian bodies on Acacia.

Food bodies

Some plants produce food bodies for use by other organisms. These small epidermal structures contain a variety of nutrients that are removed and consumed by foragers.[7] Food bodies are identified by the main nutrient they contain and by the genus of plant producing them.[7] Beltian bodies are found on the leaflet tips of Acacia plants and have relatively high protein content.[8] Beccarian bodies are found on young leaves of the genus Macaranga and are especially rich in lipids. Lipids are also the main nutrient found in pearl bodies, found on the leaves and stems of Ochroma plants. Most ant inhabitants of Cecropia plants harvest the last type of food body, as their primary food source. Remarkably these Müllerian bodies, found on the stalk of the leaf, are primarily glycogen. Glycogen is the principal storage carbohydrate found in animals and is extremely rare in plants.[7]

Nutrient content of various food bodies
Food Bodies
Main Nutrient Contained
Plant Genus
Location on Plants
Beltian bodiesProtein  Acacia Leaflet tips  
Beccarian bodiesLipids  Macaranga Young leaves  
Pearl bodiesLipids  Ochroma Leaves and stems  
Müllerian bodiesGlycogen  Cecropia Petiole of the leaf  
Extrafloral nectaries on the petiole of a Prunus avium leaf.

Extrafloral nectaries

Extrafloral nectaries are sugar-producing glands found outside the flower structures of plants. They occur in many different plant species around the world and are most commonly associated with vegetative structures that normally do not have nectaries, such as leaves, stems, and twigs.[3] These secreting structures are often non-exclusive in that nectar can be taken by a variety of animals; however, in some obligate myrmecophyte plants such as Acacia collinsii, extrafloral nectar is modified to be attractive only to the ant partners in the symbiosis.[3][9][10] The nectar thus provided feeds ants, which in turn protect these myrmecophytes from herbivorous activity. A species of deciduous tree that displays extrafloral nectaries, Catalpa speciosa, shows a decreased loss of leaf tissue on branches protected by ants, and an increase in number of seeds produced.[3]

Types of ant-plant interactions

Ants as pollinators

Unlike their bee relatives, ants rarely pollinate plants. Various assumptions have been made as to why ants are poor pollinators, although none have been verified: a) ants do not fly limiting their transport of pollen far enough to effect cross-pollination, b) ants do not systematically forage like bees do, and c) ants are not hairy, and clean themselves too frequently to allow pollen to be carried to other plants.[11] In most cases of ant pollination, the ants are one of multiple pollinators; meaning that the plants are not completely dependent on ants for pollination. However, the orchid Leporella fimbriata can only be pollinated by its winged male ant partner (Myrmecia urens).[12]

Afzelia africana seeds bearing orange elaiosomes.

Ants and seed dispersal
Main article: myrmecochory

Myrmecochory, literally translated as "ant-dispersal," is the collection and dispersal of seeds by ants. Ants disperse more than 30% of the spring-flowering herbaceous plants in eastern North America.[7] Both the plant and the ant benefit in this scenario. The ants are provided with an elaiosome, a detachable food body found on the surface of the seed. Elaiosomes have diverse compositions, usually high in lipids and fatty acids, but also containing amino acids, sugars, and protein.[7] The ants remove the elaiosome once the seed has been transported to the colony. As a result, the seeds are safely placed in nutrient-rich substrate protected from predators, benefiting the plant with optimum establishment conditions for its seed.[7]

Ants feeding plants

Myrmecotrophy, meaning "ant-fed," is the ability of plants to absorb nutrients from debris piles left by ant nests or, in the case of Nepenthes bicalcarata, from ant egesta.[13] The tropical tree Cecropia peltata obtains 98% of its nitrogen from the waste deposited by its ant counterparts.[14]

A recent study by Chanam et al.[15] showed that plants bearing domatia can be favoured even before the establishment of a specialised protection-based symbiosis, as nutritional benefits can provided by a motley set of domatia residents that could multiple species of ant (including protective, non-protective and even plant-damaging species such as Crematogaster dohrni) as well as other invertebrates, including as arboreal earthworms. Only some individuals of the myrmecophyte Humboldtia brunonis (found in the Western Ghats of India) bear domatia on some of their branches, while all individuals produce extrafloral nectar. Each domatium is formed by modified swollen and hollow internodes. These domatia have a self-opening slit that allows access to the domatium interior and are prone to interloping residents (including many species of non-protective ants and the arboreal earthworm Perionyx pullus) in addition to the protective ants.

Earlier studies established that domatia-bearing H. brunonis plants have greater fruit set, hence greater reproductive success, than H. brunonis plants without domatia. Plant tissues near domatia received 17% and 9% of their nitrogen from the ants (protective and non-protective) and the earthworm respectively. The absorbed nutrients also travelled to distant branches; hence, fruit set was not different between branches with and without domatia. This study demonstrated that non-protective interlopers in the domatia still contribute to the greater wellbeing of the plant by contributing to plant nutrition.

Ants collaborating to dismember an intruding ant.

Ants as defense

Since plants provide essential resources for ants, the need to protect the plant and those resources is extremely important. Many myrmecophytes are defended from both herbivores and other competing plants by their ant symbionts.[7] Acacia cornigera, for example, is thoroughly guarded by its obligate ant partner, Pseudomyrmex ferruginea. A single colony of P. ferruginea may contain more than 30,000 ants, and can tend multiple Acacia trees.[7] The soldier ants are extremely aggressive, patrolling the trees twenty-four hours a day. Any disturbance to the tree alerts ants, who then recruit more workers from inside the horn domatia. These ants defend the Acacia by biting, violently stinging, and pruning any trespassers. The ants keep the plant free from other insects and vertebrate herbivores, from invading fungi and also from other plants.[7]

gollark: Hey, I'm not saying the u16 is the wrong choice here, just that it also isn't really always right.
gollark: CBOR and whatnot are nicer than using custom binary formats if you plan to swap data between systems a lot, because you can add new fields without breaking things and there's parsers for basically every languæge.
gollark: (yes, this is impossible, but oh well)
gollark: Compression.
gollark: CBOR is better for data interchange, though, since it's at least partly selfdocumenting and more extensible.

See also

Notes
  1. Speight, Hunter & Watt 2008
  2. Wilson 1971
  3. Koptur 1991
  4. Fiala, Maschwitz & Pong 1991
  5. Janzen 1966
  6. Jebb 1991
  7. Rico-Gray & Oliveira 2007
  8. Heil, M; B. Baumann; R. Kruger; K.E. Linsenmair (March 2004). "Main nutrient compounds in food bodies of Mexican Acacia ant-plants". Chemoecology. 14 (1): 45–52. doi:10.1007/s00049-003-0257-x.
  9. Heil, M.; J. Rattke; W. Boland (April 2005). "Postsecretory Hydrolysis of Nectar Sucrose and Specialization in Ant/Plant Mutualism". Science. 308 (5721): 560–563. doi:10.1126/science.1107536. JSTOR 3841308. PMID 15845855.
  10. Gonzalez-Teuber, Marcia; M. Heil (April 2009). "The Role of Extrafloral Nectar Amino Acids for the Preferences of Facultative and Obligate Ant Mutualists". Journal of Chemical Ecology. 35 (4): 459–468. doi:10.1007/s10886-009-9618-4. PMID 19370376.
  11. Beattie & Hughes 2002
  12. Peakall, Handel & Beattie 1991
  13. Bazile, V.; Moran, J.A.; Moguédec, G. Le; Marshall, D.J.; Gaume, L. (2012). "A carnivorous plant fed by its ant symbiont: a unique multi-faceted nutritional mutualism". PLoS ONE. 7 (5): e36179. doi:10.1371/journal.pone.0036179. PMC 3348942. PMID 22590524.
  14. Benzing 1991
  15. Chanam, J., Sheshshayee, M.S., Kasinathan, S., Jagdeesh, A., Joshi, K.A., Borges, R.M., "Nutritional benefits from domatia inhabitants in an ant–plant interaction: interlopers do pay the rent" (Functional Ecology, 2014), doi:10.1111/1365-2435.12251

References
  • Beattie, Andrew J.; Hughes, Lesley (2002). "Ant-plant interactions". In Herrera, Carlos M.; Pellmyr, Olle (eds.). Plant-Animal Interactions. Malden, MA: Blackwell Publishing. pp. 211–235.CS1 maint: ref=harv (link)
  • Benzing, David H. (1991). "Myrmecotrophy: origins, operation, and importance". In Huxley, Camilla R.; Cutler, David F. (eds.). Ant-Plant Interactions. New York, NY: Oxford University Press. pp. 353–373. ISBN 0-19-854639-4.CS1 maint: ref=harv (link)
  • Fiala, Brigitte; Maschwitz, Ulrich; Pong, Tho Yow (1991). "The association between Macaranga trees and ants in South-east Asia". In Huxley, Camilla R.; Cutler, David F. (eds.). Ant-Plant Interactions. New York, NY: Oxford University Press. pp. 263–270. ISBN 0-19-854639-4.CS1 maint: ref=harv (link)
  • Gonzalez-Teuber, M.; Heil, M. (2009). "The Role of Extrafloral Nectar Amino Acids for the Preferences of Facultative and Obligate Ant Mutualists". Journal of Chemical Ecology. 35 (4): 459–468. doi:10.1007/s10886-009-9618-4. PMID 19370376.CS1 maint: ref=harv (link)
  • Heil, M.; Baumann, B.; Kruger, R.; Linsenmair, K.E. (2004). "Main nutrient compounds in food bodies of Mexican Acacia ant-plants". Chemoecology. 14: 45–52. doi:10.1007/s00049-003-0257-x.CS1 maint: ref=harv (link)
  • Heil, M.; Rattke, J.; Boland, W. (2005). "Postsecretory hydrolysis of nectar sucrose and specialization in ant/plant mutualism". Science. 308 (5721): 560–563. doi:10.1126/science.1107536. PMID 15845855.CS1 maint: ref=harv (link)
  • Janzen, D. H. (1966). "Coevolution of mutualism between ants and acacias in Central America". Evolution. 20 (3): 249–275. doi:10.2307/2406628. JSTOR 2406628. PMID 28562970.CS1 maint: ref=harv (link)
  • Jebb, Matthew (1991). "Cavity structure and function in the tuberous Rubiaceae". In Huxley, Camilla R.; Cutler, David F. (eds.). Ant-Plant Interactions. New York, NY: Oxford University Press. pp. 374–389. ISBN 0-19-854639-4.CS1 maint: ref=harv (link)
  • Koptur, Suzanne (1991). "Extrafloral nectarines of herbs and trees: modeling the interaction with ants and parasitoids". In Huxley, Camilla R.; Cutler, David F. (eds.). Ant-Plant Interactions. New York, NY: Oxford University Press. pp. 213–230. ISBN 0-19-854639-4.CS1 maint: ref=harv (link)
  • Peakall, Rod; Handel, Steven N.; Beattie, Andrew J. (1991). "The evidence for and importance of ant pollination". In Huxley, Camilla R.; Cutler, David F. (eds.). Ant-Plant Interactions. New York, NY: Oxford University Press. pp. 421–429. ISBN 0-19-854639-4.CS1 maint: ref=harv (link)
  • Rico-Gray, Victor; Oliveira, Paulo S (2007). The Ecology and Evolution of Ant-Plant Interactions. Chicago, IL: University of Chicago Press. pp. 42–51, 101–109.CS1 maint: ref=harv (link)
  • Speight, Martin R.; Hunter, Mark D.; Watt, Allan D. (2008). Ecology of Insects (2nd ed.). West Sussex, UK: Wiley Blackwell Publications. pp. 212–216.CS1 maint: ref=harv (link)
  • Wilson, Edward O. (1971). The Insect Societies. Belknap Press. ISBN 978-0-674-45490-3.CS1 maint: ref=harv (link)
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