| Temnothorax albipennis | |
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Scientific classification  | |
| Kingdom: | Animalia |
| Phylum: | Arthropoda |
| Class: | Insecta |
| Order: | Hymenoptera |
| Family: | Formicidae |
| Subfamily: | Myrmicinae |
| Genus: | Temnothorax |
| Species: | T. albipennis |
| Binomial name | |
| Temnothorax albipennis Curtis, 1854 | |
| Synonyms | |
T. tuberointerruptus | |
Temnothorax albipennis, the rock ant is a species of small ant in the subfamily Myrmicinae. It occurs in Europe and builds simple nests in rock crevices.
This species has the typical ant body pattern of head, mesosoma and metasoma, with the first two segments of the metasoma forming a distinct waist. It is light brown and has a few short pale coloured hairs. The antennae are elbowed and there are a pair of compound eyes and three ocelli.
As with other ants, there is a single, relatively large queen that lays eggs in the nest and a large number of workers. These are all non-breeding females and leave the nest to forage and collect building materials for its construction and repair. [1]
T. albipennis builds simple nests in cracks in rocks, enclosed by walls built from tiny pebbles and grains of sand. In an experiment where two sizes of sand grain were offered to ants that were foraging for building materials, the ants always chose the smaller grains although this was wasteful in terms of building efficiency. [2] T. albipennis scouts show behavioural lateralization when exploring unknown nest sites, showing a population-level bias to prefer left turns. One possible reason for this is that its environment is partly maze-like and consistently turning in one direction is a good way to search and exit mazes without getting lost. [3] This turning bias is correlated with slight asymmetries in the ants' compound eyes (differential ommatidia count). [4] Another experiment examined the division of labour in ant colonies and found that there tended to be a few high performance workers in small colonies which performed tasks considerably more efficiently than the other workers. This was not the case in larger colonies, and in both cases, there were a high proportion of inactive workers. [5]
Ants are one of the most successful insects on the planet and there is a long-held view that this is because of the division of labour and the way certain workers specialise in certain tasks. An experiment was carried out to examine whether these specialist ants actually performed the task better than other workers. The ants were marked with drops of paint and then were videotaped while they performed such tasks as foraging, transporting the brood and nest building. The conclusions were that, though some ants performed a range of jobs and others specialised in a single task, the latter were found not to be any more efficient at their selected tasks than were the generalists. However the specialists did put in more time on the job than the other ants so the colony overall benefited from their specialisation. [6] Research tracking T. albipennis movements found that they move in similar ways both outside and inside the nest, suggesting that workers are principally generalists equipped to do multiple tasks. The duration of each new ant movement appears to be predetermined to some degree (this is known as motor planning), which may make navigating their complex society easier. [7] [8] However, a reanalysis of the same data reached a different conclusion, [9] suggesting that the previous conclusions need further justification. Another behaviour exhibited by colonies of this species is the ability to react to predator attacks as a single unit. It has been shown that colonies will respond differentially to predation events dependent on their location within the colony, and workers will withdraw or disperse appropriately to enable effective mitigation of mortality. [10]
Ants of this species have been observed teaching each other through a process known as tandem running. An experienced forager leads a naïve nest-mate to a newly discovered resource such as food or an empty nest site. The follower obtains knowledge of the route by following in the footsteps of the tutor, maintaining contact with its antennae. Both leader and follower are aware of the progress made by the other with the leader slowing when the follower lags and speeding up when the follower gets too close. [11] Depending on how far away a new resource is, colonies will modulate the number of tandem runs that they perform, with a greater number of tandem runs occurring when the desired resource is more distant. [12] Furthermore, the relative contribution that workers make to this process differs widely among individuals, with certain ants attempting many more tandem runs than others. [13]
Ants are eusocial insects of the family Formicidae and, along with the related wasps and bees, belong to the order Hymenoptera. Ants appear in the fossil record across the globe in considerable diversity during the latest Early Cretaceous and early Late Cretaceous, suggesting an earlier origin. Ants evolved from vespoid wasp ancestors in the Cretaceous period, and diversified after the rise of flowering plants. More than 13,800 of an estimated total of 22,000 species have been classified. They are easily identified by their geniculate (elbowed) antennae and the distinctive node-like structure that forms their slender waists.
Termites are eusocial insects that are classified at the taxonomic rank of infraorder Isoptera, or alternatively as epifamily Termitoidae, within the order Blattodea. Termites were once classified in a separate order from cockroaches, but recent phylogenetic studies indicate that they evolved from cockroaches, as they are deeply nested within the group, and the sister group to wood eating cockroaches of the genus Cryptocercus. Previous estimates suggested the divergence took place during the Jurassic or Triassic. More recent estimates suggest they have an origin during the Late Jurassic, with the first fossil records in the Early Cretaceous. About 3,106 species are currently described, with a few hundred more left to be described. Although these insects are often called "white ants", they are not ants, and are not closely related to ants.
A compound eye is a visual organ found in arthropods such as insects and crustaceans. It may consist of thousands of ommatidia, which are tiny independent photoreception units that consist of a cornea, lens, and photoreceptor cells which distinguish brightness and color. The image perceived by this arthropod eye is a combination of inputs from the numerous ommatidia, which are oriented to point in slightly different directions. Compared with single-aperture eyes, compound eyes have poor image resolution; however, they possess a very large view angle and the ability to detect fast movement and, in some cases, the polarization of light.
Fungus-growing ants comprise all the known fungus-growing ant species participating in ant–fungus mutualism. They are known for cutting grasses and leaves, carrying them to their colonies' nests, and growing fungi on them on which they later feed.
An ant colony is the basic unit around which ants organize their lifecycle. Ant colonies are eusocial, communal, and efficiently organized and are very much like those found in other social Hymenoptera, though the various groups of these developed sociality independently through convergent evolution. The typical colony consists of one or more egg-laying queens, numerous sterile females and, seasonally, many winged sexual males and females. In order to establish new colonies, ants undertake flights that occur at species-characteristic times of the day. Swarms of the winged sexuals depart the nest in search of other nests. The males die shortly thereafter, along with most of the females. A small percentage of the females survive to initiate new nests.
Pogonomyrmex barbatus is a species of harvester ant from the genus Pogonomyrmex. Its common names include red ant and red harvester ant. These large ants prefer arid chaparral habitats and are native to the Southwestern United States. Nests are made underground in exposed areas. Their diets consist primarily of seeds, and they consequently participate in myrmecochory, an ant-plant interaction through which the ants gain nutrients and the plants benefit through seed dispersal. Red harvester ants are often mistaken for fire ants, but are not closely related to any fire ant species, native or introduced.
A decentralised system in systems theory is a system in which lower level components operate on local information to accomplish global goals. The global pattern of behaviour is an emergent property of dynamical mechanisms that act upon local components, such as indirect communication, rather than the result of a central ordering influence of a centralised system.
The name army ant (or legionary ant or marabunta) is applied to over 200 ant species in different lineages. Because of their aggressive predatory foraging groups, known as "raids", a huge number of ants forage simultaneously over a limited area.
Spatial organization can be observed when components of an abiotic or biological group are arranged non-randomly in space. Abiotic patterns, such as the ripple formations in sand dunes or the oscillating wave patterns of the Belousov–Zhabotinsky reaction emerge after thousands of particles interact millions of times. On the other hand, individuals in biological groups may be arranged non-randomly due to selfish behavior, dominance interactions, or cooperative behavior. W. D. Hamilton (1971) proposed that in a non-related "herd" of animals, spatial organization is likely a result of the selfish interests of individuals trying to acquire food or avoid predation. On the other hand, spatial arrangements have also been observed among highly related members of eusocial groups, suggesting that the arrangement of individuals may provide some advantage for the group.
Tandem running is a social learning phenomenon seen mostly in ants, by which one ant leads another native ant from the nest to the food source it has found. Tandem running is also used to find and choose better, new nest sites to which the colony can emigrate. The follower ant maintains contact with the lead ant by frequently touching the leader's legs and abdomen with its antennae. As predators, scavengers, and herbivores, ants have a variety of food sources, for which they may journey as far as 200 meters from their nest, spraying a scent trail as they go. To lead their kin to new food sources, ants demonstrate one of the few examples of interactive teaching outside of the mammalian class. Social learning by teaching requires that the naive observer change its behavior and acquire some skills or knowledge faster than it would have independently and that the teacher incur some cost. In order for the follower ant to learn landmarks, the leader must travel much slower and make frequent stops to check for his follower. Ultimately, the knowledge of the route to the new food source can be passed throughout the colony as one follower becomes a leader, making tandem running an effective time-saving practice.
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.
Worker policing is a behavior seen in colonies of social hymenopterans whereby worker females eat or remove eggs that have been laid by other workers rather than those laid by a queen. Worker policing ensures that the offspring of the queen will predominate in the group. In certain species of bees, ants and wasps, workers or the queen may also act aggressively towards fertile workers. Worker policing has been suggested as a form of coercion to promote the evolution of altruistic behavior in eusocial insect societies.
Leptothorax acervorum is a small brown to yellow ant in the subfamily Myrmicinae. It was first described by Johan Christian Fabricius in 1793. L. acervorum is vastly distributed across the globe, most commonly found in the coniferous forests of Central, Western and Northern Europe. The morphology of L. acervorum is extremely similar to that of other Leptothorax ants. The difference arises in the two-toned appearance of L. acervorum, with the head and metasoma being darker than the mesosoma segment of the body, and hair across its body. Following Bergmann's rule—unusually, for ectothermic animals—body size increases with latitude.
Temnothorax is a genus of ants in the subfamily Myrmicinae. It contains more than 350 species.
Megaponera analis is the sole species of the genus Megaponera. They are a strictly termite-eating (termitophagous) ponerine ant species widely distributed in Sub-Saharan Africa and most commonly known for their column-like raiding formation when attacking termite feeding sites. Their sophisticated raiding behaviour gave them the common name Matabele ant after the Matabele tribe, fierce warriors who overwhelmed various other tribes during the 1800s. With some individuals reaching up to 25 millimetres (0.98 in) in length, M. analis is one of the world's largest ants.
Temnothorax rugatulus is a species of ant in the genus Temnothorax. It is found in North America. More specifically, it is found in the forests of the western United States. Colonies are either monogynous or polygynous. Queens in monogynous colonies are generally larger (marcogynes), about twice the size of conspecific workers; polygynous colonies have smaller queens (microgynes), typically slightly smaller than the workers. T. rugatulus ants are a subdominant ant group.
Social immunity is any antiparasite defence mounted for the benefit of individuals other than the actor. For parasites, the frequent contact, high population density and low genetic variability makes social groups of organisms a promising target for infection: this has driven the evolution of collective and cooperative anti-parasite mechanisms that both prevent the establishment of and reduce the damage of diseases among group members. Social immune mechanisms range from the prophylactic, such as burying beetles smearing their carcasses with antimicrobials or termites fumigating their nests with naphthalene, to the active defenses seen in the imprisoning of parasitic beetles by honeybees or by the miniature 'hitchhiking' leafcutter ants which travel on larger worker's leaves to fight off parasitoid flies. Whilst many specific social immune mechanisms had been studied in relative isolation, it was not until Sylvia Cremer et al.'s 2007 paper "Social Immunity" that the topic was seriously considered. Empirical and theoretical work in social immunity continues to reveal not only new mechanisms of protection but also implications for understanding of the evolution of group living and polyandry.
Anomotaenia brevis is a tapeworm which has been found to be one of many parasite species able to manipulate their host's behavior. Host manipulation is commonly observed in parasites with complex life cycles reliant on multiple hosts for development. While the definitive host for A. brevis is the woodpecker, their intermediate host is the Temnothoraxnylanderi, a species of ant located in the oak forests of western Europe. The tapeworm alters the appearance and behavior of the T. nylanderi ant in order to ensure transmission to the woodpecker, where it can complete its life cycle.
Nigel R. Franks is an English emeritus professor of Animal Behaviour and Ecology at the University of Bristol. He obtained a BSc and PhD in biology at the University of Leeds. After receiving his BSc in 1977 he began his PhD, during which he spent two years doing field work in Panama on army ants with the Smithsonian Tropical Research Institute. He was awarded the Thomas Henry Huxley Award in 1980 from the Zoological Society of London for the best British PhD in Zoology. He then received a Postdoctoral Fellowship from the Royal Commission for the Great Exhibition of 1851 allowing him to undertake postdoctoral work under Edward O. Wilson at Harvard University before becoming a lecturer at the University of Bath in 1982, later being promoted to full professor in 1995. He moved to the University of Bristol in 2001. He is renowned for his studies of collective animal behaviour, particularly of ant colonies. His Ant Lab at Bristol pioneered the use of Temnothorax as a model ant species for the study of collective decision-making and complex systems. In a 2009 profile in Science he discusses his pioneering use of radio-frequency identification tags (RFID) glued to the backs of each ant for tracking individuals in their society. His book Social evolution in ants with Andrew Bourke was an important contribution to the understanding of kin selection theory and sex ratio theory with respect to social evolution in insects, while his co-authored book Self-organization in biological systems has been cited well over 3000 times
Insect cognition describes the mental capacities and study of those capacities in insects. The field developed from comparative psychology where early studies focused more on animal behavior. Researchers have examined insect cognition in bees, fruit flies, and wasps.
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