Colony (biology)

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A colony of Brandt's cormorants in Point Lobos, California Phalacrocorax penicillatus (Brandt's Cormorant) colony, Point Lobos - Diliff.jpg
A colony of Brandt's cormorants in Point Lobos, California

In biology, a colony is composed of two or more conspecific individuals living in close association with, or connected to, one another. This association is usually for mutual benefit such as stronger defense or the ability to attack bigger prey. [1]

Contents

Colonies can form in various shapes and ways depending on the organism involved. For instance, the bacterial colony is a cluster of identical cells (clones). These colonies often form and grow on the surface of (or within) a solid medium, usually derived from a single parent cell. [2]

Colonies, in the context of development, may be composed of two or more unitary (or solitary) organisms or be modular organisms. Unitary organisms have determinate development (set life stages) from zygote to adult form and individuals or groups of individuals (colonies) are visually distinct. Modular organisms [3] have indeterminate growth forms (life stages not set) through repeated iteration of genetically identical modules (or individuals), and it can be difficult to distinguish between the colony as a whole and the modules within. [4] In the latter case, modules may have specific functions within the colony.

In contrast, solitary organisms do not associate with colonies; they are ones in which all individuals live independently and have all of the functions needed to survive and reproduce.

Some organisms are primarily independent and form facultative colonies in reply to environmental conditions while others must live in a colony to survive (obligate). For example, some carpenter bees will form colonies when a dominant hierarchy is formed between two or more nest foundresses [5] (facultative colony), while corals are animals that are physically connected by living tissue (the coenosarc) that contains a shared gastrovascular cavity.

Colony types

Social colonies

A breeding colony of northern gannets on the Heligoland archipelago in the North Sea. Colony Northern Gannet Morus bassanus.jpg
A breeding colony of northern gannets on the Heligoland archipelago in the North Sea.

Unicellular and multicellular unitary organisms may aggregate to form colonies. For example,

Modular organisms

The pelagic Marrus orthocanna is a colonial siphonophore assembled from two types of zooids Marrus orthocanna.jpg
The pelagic Marrus orthocanna is a colonial siphonophore assembled from two types of zooids

Modular organisms are those in which a genet (or genetic individual formed from a sexually-produced zygote) asexually reproduces to form genetically identical clones called ramets. [8]

A clonal colony is when the ramets of a genet live in close proximity or are physically connected. Ramets may have all of the functions needed to survive on their own or be interdependent on other ramets. For example, some sea anemones go through the process of pedal laceration in which a genetically identical individual is asexually produced from tissue broken off from the anemone's pedal disc. In plants, clonal colonies are created through the propagation of genetically identical trees by stolons or rhizomes.

Colonial organisms are clonal colonies composed of many physically connected, interdependent individuals. The subunits of colonial organisms can be unicellular, as in the alga Volvox (a coenobium), or multicellular, as in the phylum Bryozoa. Colonial organisms may have been the first step toward multicellular organisms. [9] Individuals within a multicellular colonial organism may be called ramets, modules, or zooids. Structural and functional variation (polymorphism), when present, designates ramet responsibilities such as feeding, reproduction, and defense. To that end, being physically connected allows the colonial organism to distribute nutrients and energy obtained by feeding zooids throughout the colony. The hydrozoan Portuguese man o' war is a classic example of a colonial organism, one of many in the taxonomic class. [10]

Microbial colonies

A microbial colony is defined as a visible cluster of microorganisms growing on the surface of or within a solid medium, presumably cultured from a single cell. [11] Because the colony is clonal, with all organisms in it descending from a single ancestor (assuming no contamination), they are genetically identical, except for any mutations (which occur at low frequencies). Obtaining such genetically identical organisms (or pure strains) can be useful; this is done by spreading organisms on a culture plate and starting a new stock from a single resulting colony. [12]

A biofilm is a colony of microorganisms often comprising several species, with properties and capabilities greater than the aggregate of capabilities of the individual organisms[ citation needed ].

Colony ontogeny for eusocial insects

Colony ontogeny refers to the developmental process and progression of a colony. It describes the various stages and changes that occur within a colony from its initial formation to its mature state. [13] The exact duration and dynamics of colony ontogeny can vary greatly depending on the species and environmental conditions. [14] [15] Factors such as resource availability, competition, and environmental cues can influence the progression and outcome of colony development.[ citation needed ]

During colony ontogeny for eusocial insects such as ants and bees, a colony goes through several distinct phases, each characterised by specific behavioural patterns, division of labor, and structural modifications. While the exact details can vary depending on the species, the general progression typically involves a number of well-defined stages, detailed below. [16] [17]

Founding stage

In this initial stage, a single female individual or small group of female individuals, often called the foundress(es), queen(s) (and kings for termites) or primary reproductive(s), establish a new colony. The foundresses build a basic nest structure and begin to lay eggs. The foundresses can also perform non-reproductive tasks at this early stage, such as nursing these first eggs and leaving the nest to gather resources.

Worker emergence

This is also known as the ergonomic stage. As the eggs laid by the foundresses develop, they give rise to the first generation of workers. These workers can assume various tasks, such as foraging, brood care, and nest maintenance. Initially, the worker population is relatively small, and their tasks are not as specialised. As the colony grows, more workers emerge, and the division of labor becomes more pronounced. Some individuals may specialise in tasks like foraging, defense, or tending to the brood, while others may take on general tasks within the nest. [18] These specialised tasks can change throughout the life of a worker.

Reproductive phase

At a certain point in the colony ontogeny, usually after a period of growth and maturation, the colony produces reproductives, including new virgin queens (princesses) and males. These individuals have the potential to leave the nest and start new colonies, ensuring the transmission of the gene pool of its natal colony.

Colony death

Over time, colonies may go through a senescence phase where the reproductive output declines, and the colony's overall vitality diminishes. Eventually, the colony may die off or be replaced by a new generation of reproductives. After the death of the queen in a monogyne colony, possible fates other than colony death include serial polygyny (when a virgin queen of the colony replaces the dead queen as the primary reproductive) or colony inheritance (when a worker takes over as primary reproductive).[ citation needed ]

Life history

Individuals in social colonies and modular organisms receive benefit to such a lifestyle. For example, it may be easier to seek out food, defend a nesting site, or increase competitive ability against other species. Modular organisms' ability to reproduce asexually in addition to sexually allows them unique benefits that social colonies do not have. [8]

The energy required for sexual reproduction varies based on the frequency and length of reproductive activity, number and size of offspring, and parental care. [19] While solitary individuals bear all of those energy costs, individuals in some social colonies share a portion of those costs.[ citation needed ]

Modular organisms save energy by using asexual reproduction during their life. Energy reserved in this way allows them to put more energy towards colony growth, regenerating lost modules (due to predation or other cause of death), or response to environmental conditions.[ citation needed ]

See also

Related Research Articles

<span class="mw-page-title-main">Asexual reproduction</span> Reproduction without a sexual process

Asexual reproduction is a type of reproduction that does not involve the fusion of gametes or change in the number of chromosomes. The offspring that arise by asexual reproduction from either unicellular or multicellular organisms inherit the full set of genes of their single parent and thus the newly created individual is genetically and physically similar to the parent or an exact clone of the parent. Asexual reproduction is the primary form of reproduction for single-celled organisms such as archaea and bacteria. Many eukaryotic organisms including plants, animals, and fungi can also reproduce asexually. In vertebrates, the most common form of asexual reproduction is parthenogenesis, which is typically used as an alternative to sexual reproduction in times when reproductive opportunities are limited. Komodo dragons and some monitor lizards can reproduce asexually.

<span class="mw-page-title-main">Budding</span> Form of cellular asexual reproduction

Budding or blastogenesis is a type of asexual reproduction in which a new organism develops from an outgrowth or bud due to cell division at one particular site. For example, the small bulb-like projection coming out from the yeast cell is known as a bud. Since the reproduction is asexual, the newly created organism is a clone and excepting mutations is genetically identical to the parent organism. Organisms such as hydra use regenerative cells for reproduction in the process of budding.

Cheating is a term used in behavioral ecology and ethology to describe behavior whereby organisms receive a benefit at the cost of other organisms. Cheating is common in many mutualistic and altruistic relationships. A cheater is an individual who does not cooperate but can potentially gain the benefit from others cooperating. Cheaters are also those who selfishly use common resources to maximize their individual fitness at the expense of a group. Natural selection favors cheating, but there are mechanisms to regulate it. The stress gradient hypothesis states that facilitation, cooperation or mutualism should be more common in stressful environments, while cheating, competition or parasitism are common in benign environments.

Plant reproduction is the production of new offspring in plants, which can be accomplished by sexual or asexual reproduction. Sexual reproduction produces offspring by the fusion of gametes, resulting in offspring genetically different from either parent. Asexual reproduction produces new individuals without the fusion of gametes, resulting in clonal plants that are genetically identical to the parent plant and each other, unless mutations occur.

<span class="mw-page-title-main">European paper wasp</span> Species of wasp

The European paper wasp is one of the most common and well-known species of social wasps in the genus Polistes. Its diet is more diverse than those of most Polistes species—many genera of insects versus mainly caterpillars in other Polistes—giving it superior survivability compared to other wasp species during a shortage of resources.

<i>Formica polyctena</i> Species of ant

Formica polyctena is a species of European red wood ant in the genus Formica and large family Formicidae. The species was first described by Arnold Förster in 1850. The latin species name polyctena is from Greek and literally means 'many cattle', referring to the species' habit of farming aphids for honeydew food. It is found in many European countries. It is a eusocial species, that has a distinct caste system of sterile workers and a very small reproductive caste. The ants have a genetic based cue that allow them to identify which other ants are members of their nest and which are foreign individuals. When facing these types of foreign invaders the F. polyctena has a system to activate an alarm. It can release pheromones which can trigger an alarm response in other nearby ants.

Task allocation and partitioning is the way that tasks are chosen, assigned, subdivided, and coordinated within a colony of social insects. Task allocation and partitioning gives rise to the division of labor often observed in social insect colonies, whereby individuals specialize on different tasks within the colony. Communication is closely related to the ability to allocate tasks among individuals within a group. This entry focuses exclusively on social insects. For information on human task allocation and partitioning, see division of labour, task analysis, and workflow.

<span class="mw-page-title-main">Organism</span> Any individual living being or physical living system

An organism is any biological living system that functions as an individual life form. All organisms are composed of cells. The idea of organism is based on the concept of minimal functional unit of life. Three traits have been proposed to play the main role in qualification as an organism:

<span class="mw-page-title-main">Eusociality</span> Highest level of animal sociality a species can attain

Eusociality, the highest level of organization of sociality, is defined by the following characteristics: cooperative brood care, overlapping generations within a colony of adults, and a division of labor into reproductive and non-reproductive groups. The division of labor creates specialized behavioral groups within an animal society which are sometimes referred to as 'castes'. Eusociality is distinguished from all other social systems because individuals of at least one caste usually lose the ability to perform at least one behavior characteristic of individuals in another caste. Eusocial colonies can be viewed as superorganisms.

<i>Ropalidia marginata</i> Species of insect

Ropalidia marginata is an Old World species of paper wasp. It is primitively eusocial, not showing the same bias in brood care seen in other social insects with greater asymmetry in relatedness. The species employs a variety of colony founding strategies, sometimes with single founders and sometimes in groups of variable number. The queen does not use physical dominance to control workers; there is evidence of pheromones being used to suppress other female workers from overtaking queenship.

<i>Nasutitermes corniger</i> Species of termite

Nasutitermes corniger is a species of arboreal termite that is endemic to the neotropics. It is very closely related to Nasutitermes ephratae. The species has been studied relatively intensively, particularly on Barro Colorado Island, Panama. These studies and others have shown that the termite interacts with many different organisms including a bat that roosts in its nest and various species of ants that cohabit with the termite.

<i>Polistes metricus</i> Species of wasp

Polistes metricus is a wasp native to North America. In the United States, it ranges throughout the southern Midwest, the South, and as far northeast as New York, but has recently been spotted in southwest Ontario. A single female specimen has also been reported from Dryden, Maine. Polistes metricus is dark colored, with yellow tarsi and black tibia. Nests of Polistes metricus can be found attached to the sides of buildings, trees, and shrubbery.

<span class="mw-page-title-main">Halictinae</span> Subfamily of bees

Within the insect order Hymenoptera, the Halictinae are the largest, most diverse, and most recently diverged of the four halictid subfamilies. They comprise over 2400 bee species belonging to the five taxonomic tribes Augochlorini, Thrinchostomini, Caenohalictini, Sphecodini, and Halictini, which some entomologists alternatively organize into the two tribes Augochlorini and Halictini.

<i>Polistes fuscatus</i> Species of insect

Polistes fuscatus, whose common name is the dark or northern paper wasp, is widely found in eastern North America, from southern Canada through the southern United States. It often nests around human development. However, it greatly prefers areas in which wood is readily available for use as nest material, therefore they are also found near and in woodlands and savannas. P. fuscatus is a social wasp that is part of a complex society based around a single dominant foundress along with other cofoundresses and a dominance hierarchy.

Synalpheus regalis is a species of snapping shrimp that commonly live in sponges in the coral reefs along the tropical West Atlantic. They form a prominent component of the diverse marine cryptofauna of the region. For the span of their entire lives, they live in the internal canals of the host sponge, using it as a food resource and shelter. It has been shown that colonies contain over 300 individuals, but only one reproductive female. Also, larger colony members, most of which apparently never breed, defend the colony against heterospecific intruders. This evidence points towards the first known case of eusociality in a marine animal.

<i>Ooceraea biroi</i> Species of ant

Ooceraea biroi, the clonal raider ant, is a queenless clonal ant in the genus Ooceraea. Native to the Asian mainland, this species has become invasive on tropical and subtropical islands throughout the world. Unlike most ants, which have reproductive queens and mostly nonreproductive workers, all individuals in a O. biroi colony reproduce clonally via thelytokous parthenogenesis. Like most dorylines, O. biroi are obligate myrmecophages and raid nests of other ant species to feed on the brood.

<i>Halictus ligatus</i> Species of bee

Halictus ligatus is a species of sweat bee from the family Halictidae, among the species that mine or burrow into the ground to create their nests. H. ligatus, like Lasioglossum zephyrus, is a primitively eusocial bee species, in which aggression is one of the most influential behaviors for establishing hierarchy within the colony, and H. ligatus exhibits both reproductive division of labor and overlapping generations.

Belonogaster juncea juncea is a subspecies of Belonogaster juncea and is classified as a primitively eusocial wasp, meaning that the species is social while exhibiting a morphology that is indistinguishable from that of other castes. It is also classified as a type of African Paper Wasp. Many of the studies relating specifically to B. j. juncea take place at the University of Yaoundé in Cameroon.

Ropalidia fasciata, a common paper wasp, is a wide-ranging species that is distributed from India to the Lesser Sunda Islands, Palawan, and Ryukyu Islands, occupying the northern edge of Ropalidia's larger distribution. These primitively eusocial wasps are unique in that they do not exhibit the strict matrifilial, single-queen social structure found in many species of social insects. Instead, colonies are founded based on associations between several females, or 'foundresses'.

<i>Halictus sexcinctus</i> Species of bee

Halictus sexcinctus, commonly referred to as the six-banded furrow bee, is a species of sweat bee found throughout Europe and as far east as Asian Turkey and Iraq. The H. sexcinctus can be easily confused with the closely related species, Halictus scabiosae, due to very similar morphological features. H. sexcinctus show a social polymorphism in which different colonies can exhibit solitary, communal, or eusocial structure. Due to this large variance in social organization, it was suspected that it was not one species at all, but rather multiple, cryptic species. However, genetic analysis was able to confirm these varying populations as one species. H. sexcinctus will forage from multiple flower species, but prefers plant species with wide-open flowers. Their nests can be found dug into the ground in loamy or sandy soil.

References

  1. Jackson, J.B.C. (1977). "Competition on Marine Hard Substrata: The Adaptive Significance of Solitary and Colonial Strategies". The American Naturalist. 111 (980): 743–767. doi:10.1086/283203. S2CID   84687243.
  2. "Colony – Biology-Online Dictionary". www.biology-online.org. Retrieved 2017-05-06.
  3. Hiebert, Laurel S.; Simpson, Carl; Tiozzo, Stefano (2020-04-19). "Coloniality, clonality, and modularity in animals: The elephant in the room" (PDF). Journal of Experimental Zoology Part B: Molecular and Developmental Evolution. 336 (3): 198–211. doi:10.1002/jez.b.22944. ISSN   1552-5007. PMID   32306502. S2CID   216030034.
  4. Begon, Michael; et al. (2014). Essentials of Ecology (4th ed.). Wiley. ISBN   978-0-470-90913-3.
  5. Dunn, T.; Richards, M.H. (2003). "When to bee social: interactions among environmental constraints, incentives, guarding, and relatedness in a facultatively social carpenter bee". Behavioral Ecology. 14 (3): 417–424. doi: 10.1093/beheco/14.3.417 .
  6. Canciani, M.; Arnellos, A.; Moreno, A. (2019). "Revising the Superorganism: An Organizational Approach to Complex Eusociality". Frontiers in Psychology. 10: Article 2653. doi: 10.3389/fpsyg.2019.02653 . PMC   6901679 . PMID   31849768.
  7. Grove, Noel (December 1988). "Quietly Conserving Nature". National Geographic . 174 (6): 822.
  8. 1 2 Winston, J. (2010). "Life in the Colonies: Learning the Alien Ways of Colonial Organisms". Integrative and Comparative Biology. 50 (6): 919–933. doi: 10.1093/icb/icq146 . PMID   21714171.
  9. Alberts, Bruce; et al. (1994). Molecular Biology of the Cell (3rd ed.). New York: Garland Science. ISBN   0-8153-1620-8 . Retrieved 2014-06-11.
  10. "Hydrozoa". Animal Diversity Web. Retrieved 2017-05-06.
  11. Tortora, Gerard J.; Berdell R., Funke; Christine L., Case (2009). Microbiology, An Introduction . Berlin: Benjamin Cummings. pp. 170–171. ISBN   978-0-321-58420-5.
  12. Sanders, E.R. (2012). "Aseptic Laboratory Techniques: Plating Methods". Journal of Visualized Experiments (63): e3064. doi:10.3791/3064. PMC   4846335 . PMID   22617405.
  13. Jeanne, R. L. (1986). "The evolution of the organization of work in social insects". Monitore Zoologico Italiano-Italian Journal of Zoology . 20: 119–133.
  14. Keller, L. (1998). "Queen lifespan and colony characteristics in ants and termites". Insectes Sociaux . 45 (3): 235–246. doi:10.1007/s000400050084. S2CID   24541087.
  15. Keller, L.; Genoud, M. (1997). "Extraordinary lifespans in ants: A test of evolutionary theories of ageing". Nature . 389 (6654): 958–960. Bibcode:1997Natur.389..958K. doi:10.1038/40130. S2CID   4423161.
  16. Bourke, A. F. G. (1999). "Colony size, social complexity and reproductive conflict in social insects". Journal of Evolutionary Biology . 12 (2): 245–257. doi: 10.1046/j.1420-9101.1999.00028.x . S2CID   85187599.
  17. Alexander, R. D.; Noonan, K. M.; Crespi, B. J. (1991). Jablonski, N. G.; Jain, V.; Jarchow, H.; Schulze-Makuch, P.; Deutsch, T. (eds.). The evolution of eusociality. The biology of the naked mole-rat. Vol. 3. p. 44.
  18. Friedmann, D.; Johnson, B.; Linksvayer, T. (2020). "Distributed physiology and the molecular basis of social life in eusocial insects". Hormones and Behavior. 122: 104757. doi: 10.1016/j.yhbeh.2020.104757 . PMID   32305342. S2CID   216030233.
  19. Kunz, T.H.; Orrell, K.S. (2004). "Energy Costs of Reproduction". Encyclopedia of Energy. 5: 423–442. doi:10.1016/B0-12-176480-X/00061-9.