Locomotor mimicry is a subtype of Batesian mimicry in which animals avoid predation by mimicking the movements of another species phylogenetically separated. [1] This can be in the form of mimicking a less desirable species or by mimicking the predator itself. [1] Animals can show similarity in swimming, walking, or flying of their model animals.
The complex interaction between mimics, models, and predators (sometimes called observers) can help explain similarities amongst species beyond ideas that emerge from evolutionary comparative approaches. [2] In terms of overall movement, the continuous locomotor mimicry of a species that differs anatomically from the mimic may increase metabolic cost. However, the benefit of avoiding predation appears to outweigh the increased energy cost, because mimicking animals tend to have higher survival rates than their non-mimicking counterparts. [3]
The most common form of locomotor terrestrial mimicry is found in ant-mimicking spiders. [4] These mimics are capable of antennal illusions and similar gait patterns as an ant, which is shown in the jumping spider family (Araneae, Salticidae). [2] Ants appear to be beneficial models because they possess effective protective traits such as, chemical defences, and aggressiveness. Spiders, however, lack some of these specialized traits and therefore by acting as an ant, may avoid predation because the predator has less desire for ants.
Mimetic jumping spiders imitate the zig-zag trajectories of ants, which appears to be beneficial for avoiding predators that are from an elevated vantage point. [2] However, this may be an example of imperfect mimicry because the spiders display this behaviour in settings where ants do not.
It was once thought that these ant-mimicking spiders walk on 6 legs instead of 8 so that they could use a set of legs to mimic ant antennae. [5] However, further analysis revealed that the spiders only do this whilst stationary, which leads to the assumption that there may be a limit to the neural circuitry underlying limb movement that does not allow them to move on 6 legs. [2] This antennal mimicry appears to be most beneficial whilst in a close proximity to a predator.
Another example of terrestrial locomotor mimicry is seen in salticid-mimicking moths. [3] The moths fan out their hind wings and their forewings are raised above their bodies. In this position, the moth's wings look like salticid legs. Moths that resemble the appearance and locomotion of predatory spiders are preyed upon less by the spiders. [6] The spiders will even display courtship or territorial behaviour towards the mimics, indicating that the spiders misidentify the moths as conspecifics. [6] Even if the spiders eventually eat the moths, the time it takes for the first attack to occur is longer than the time taken to attack non-mimetic moths.
In butterflies, it is thought that palatability to predators is related to flight components. [7] Typically, fast-flying prey are more palatable, whereas unpalatable species tend to fly more slowly. These flight characteristics could help predators recognize prey as being palatable or unpalatable. Researchers compared the flight patterns of palatable non-mimetic, palatable mimetic, and unpalatable butterflies by looking at directional flight changes of each species. [7] It was determined that the palatable mimetic butterfly species had a significantly different flight pattern compared to the palatable non-mimetic. The palatable mimetic species had a flight pattern that resembled that of their unpalatable models.
Another example of aerial locomotor mimicry is found in the common drone fly (Eristalis tenax) and its presumed model, the western honey bee (Apis mellifera). [8] In analyses of flight sequences, flight velocities, flight trajectories, and time spent hovering, it was found that the flight patterns of common drone flies were more similar to honey bees than to that of other flies. The drone flies and their models both exhibit loops in their flight paths, which is surprising for the drone flies because they are very adept fliers. [8] A likely explanation for this flight behaviour is that, while foraging, the drone flies are at increased risk of predation by birds and therefore they alter their flying to resemble the noxious honeybee and avoid predation. [8]
The ghost pipefish is able to blend into its surroundings due to its similarity in colour and motion to sea plants. [9] [10] In order to avoid predators, the organism will sway in the water to resemble underwater vegetation as much as possible.
In evolutionary biology, mimicry is an evolved resemblance between an organism and another object, often an organism of another species. Mimicry may evolve between different species, or between individuals of the same species. In the simplest case, as in Batesian mimicry, a mimic resembles a model, so as to deceive a dupe, all three being of different species. A Batesian mimic, such as a hoverfly, is harmless, while its model, such as a wasp, is harmful, and is avoided by the dupe, such as an insect-eating bird. Birds hunt by sight, so the mimicry in that case is visual, but in other cases mimicry may make use of any of the senses. Most types of mimicry, including Batesian, are deceptive, as the mimics are not harmful, but Müllerian mimicry, where different harmful species resemble each other, is honest, as when species of wasps and of bees all have genuinely aposematic warning coloration. More complex types may be bipolar, involving only two species, such as when the model and the dupe are the same; this occurs for example in aggressive mimicry, where a predator in wolf-in-sheep's-clothing style resembles its prey, allowing it to hunt undetected. Mimicry is not limited to animals; in Pouyannian mimicry, an orchid flower is the mimic, resembling a female bee, its model; the dupe is the male bee of the same species, which tries to copulate with the flower, enabling it to transfer pollen, so the mimicry is again bipolar. In automimicry, another bipolar system, model and mimic are the same, as when blue lycaenid butterflies have 'tails' or eyespots on their wings that mimic their own heads, misdirecting predator dupes to strike harmlessly. Many other types of mimicry exist.
Batesian mimicry is a form of mimicry where a harmless species has evolved to imitate the warning signals of a harmful species directed at a predator of them both. It is named after the English naturalist Henry Walter Bates, who worked on butterflies in the rainforests of Brazil.
Anti-predator adaptations are mechanisms developed through evolution that assist prey organisms in their constant struggle against predators. Throughout the animal kingdom, adaptations have evolved for every stage of this struggle, namely by avoiding detection, warding off attack, fighting back, or escaping when caught.
The viceroy is a North American butterfly. It was long thought to be a Batesian mimic of the monarch butterfly, but since the viceroy is also distasteful to predators, it is now considered a Müllerian mimic instead.
Müllerian mimicry is a natural phenomenon in which two or more well-defended species, often foul-tasting and sharing common predators, have come to mimic each other's honest warning signals, to their mutual benefit. The benefit to Müllerian mimics is that predators only need one unpleasant encounter with one member of a set of Müllerian mimics, and thereafter avoid all similar coloration, whether or not it belongs to the same species as the initial encounter. It is named after the German naturalist Fritz Müller, who first proposed the concept in 1878, supporting his theory with the first mathematical model of frequency-dependent selection, one of the first such models anywhere in biology.
Aposematism is the advertising by an animal, whether terrestrial or marine, to potential predators that it is not worth attacking or eating. This unprofitability may consist of any defenses which make the prey difficult to kill and eat, such as toxicity, venom, foul taste or smell, sharp spines, or aggressive nature. These advertising signals may take the form of conspicuous coloration, sounds, odours, or other perceivable characteristics. Aposematic signals are beneficial for both predator and prey, since both avoid potential harm.
In ecology, crypsis is the ability of an animal or a plant to avoid observation or detection by other animals. It may be a predation strategy or an antipredator adaptation. Methods include camouflage, nocturnality, subterranean lifestyle and mimicry. Crypsis can involve visual, olfactory or auditory concealment. When it is visual, the term cryptic coloration, effectively a synonym for animal camouflage, is sometimes used, but many different methods of camouflage are employed by animals or plants.
The queen butterfly is a North and South American butterfly in the family Nymphalidae with a wingspan of 80–85 mm. It is orange or brown with black wing borders and small white forewing spots on its dorsal wing surface, and reddish ventral wing surface fairly similar to the dorsal surface. The ventral hindwings have black veins and small white spots in a black border. The male has a black androconial scent patch on its dorsal hindwings. It can be found in meadows, fields, marshes, deserts, and at the edges of forests.
Ant mimicry or myrmecomorphy is mimicry of ants by other organisms; it has evolved over 70 times. Ants are abundant all over the world, and potential predators that rely on vision to identify their prey, such as birds and wasps, normally avoid them, because they are either unpalatable or aggressive. Some arthropods mimic ants to escape predation, while some predators of ants, especially spiders, mimic them anatomically and behaviourally in aggressive mimicry. Ant mimicry has existed almost as long as ants themselves; the earliest ant mimics in the fossil record appear in the mid-Cretaceous alongside the earliest ants.
Anatea formicaria is an ant-mimicking spider. It is only known from the rain forest of New Caledonia. Before 1967, it was considered to belong to the family Clubionidae. It was placed there based on the ant-like outward modifications and male genitalia, which superficially resemble those of the genus Micaria. In fact it is closely related to the genera Euryopis and possibly Achaearanea.
In zoology, automimicry, Browerian mimicry, or intraspecific mimicry, is a form of mimicry in which the same species of animal is imitated. There are two different forms.
Aggressive mimicry is a form of mimicry in which predators, parasites, or parasitoids share similar signals, using a harmless model, allowing them to avoid being correctly identified by their prey or host. Zoologists have repeatedly compared this strategy to a wolf in sheep's clothing. In its broadest sense, aggressive mimicry could include various types of exploitation, as when an orchid exploits a male insect by mimicking a sexually receptive female, but will here be restricted to forms of exploitation involving feeding. For example, indigenous Australians who dress up as and imitate kangaroos when hunting would not be considered aggressive mimics, nor would a human angler, though they are undoubtedly practising self-decoration camouflage. Treated separately is molecular mimicry, which shares some similarity; for instance a virus may mimic the molecular properties of its host, allowing it access to its cells. An alternative term, Peckhamian mimicry, has been suggested, but it is seldom used.
In evolutionary biology, Gilbertian mimicry is a rare type of mimicry involving only two species, a host or prey animal which is the mimic, and its parasite or predator, which is both the model for the mimicry, and the dupe that is deceived by it. The mechanism provides a measure of protection for the mimic, as parasites and predators rarely attack their own species.
Emsleyan mimicry, also called Mertensian mimicry, describes an unusual type of mimicry where a deadly prey mimics a less dangerous species.
Chemical mimicry is a type of biological mimicry involving the use of chemicals to dupe an operator.
In evolutionary biology, mimicry in plants is where a plant evolves to resemble another organism physically or chemically. Mimicry in plants has been studied far less than mimicry in animals. It may provide protection against herbivory, or may deceptively encourage mutualists, like pollinators, to provide a service without offering a reward in return.
Animal Coloration, or in full Animal Coloration: An Account of the Principal Facts and Theories Relating to the Colours and Markings of Animals, is a book by the English zoologist Frank Evers Beddard, published by Swan Sonnenschein in 1892. It formed part of the ongoing debate amongst zoologists about the relevance of Charles Darwin's theory of natural selection to the observed appearance, structure, and behaviour of animals, and vice versa.
Camponotus planatus, known generally as the compact carpenter ant or short carpenter ant, is one of three Camponotus species that is polygynous, or has more than one queen. It is a species of ant.
Mallophora bomboides, also known as the Florida bee killer, is a predaceous species of robber fly of the family Asilidae that feeds primarily on bumblebees. M. bomboides is a noteworthy instance of Batesian mimicry given its close resemblance to its prey, the bumblebee. These bees are typically found in the Eastern and Southern regions of the United States like South Carolina and Florida.
In evolutionary biology, mimicry in vertebrates is mimicry by a vertebrate of some model, deceiving some other animal, the dupe. Mimicry differs from camouflage as it is meant to be seen, while animals use camouflage to remain hidden. Visual, olfactory, auditory, biochemical, and behavioral modalities of mimicry have been documented in vertebrates.