Mimicry in plants

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The climber Boquila trifoliata is thought to vary its leaf shape to resemble the plant it is climbing on, perhaps reducing its conspicuousness to herbivores. Boquila trifoliolata (Valdivia, Chili).jpg
The climber Boquila trifoliata is thought to vary its leaf shape to resemble the plant it is climbing on, perhaps reducing its conspicuousness to herbivores.

In evolutionary biology, mimicry in plants is where a plant organism evolves to resemble another organism physically or chemically, increasing the mimic's Darwinian fitness. Mimicry in plants has been studied far less than mimicry in animals, with fewer documented cases and peer-reviewed studies. However, it may provide protection against herbivory, or may deceptively encourage mutualists, like pollinators, to provide a service without offering a reward in return. [2]

Contents

Types of plant mimicry include Bakerian, where female flowers imitate males of the same species, Müllerian mimicry of the flower or fruit, where a plant mimics a rewarding flower (Dodsonian), luring pollinators by mimicking another species of flower, or fruit where feeders of the other species are attracted to a fake fruit to distribute seeds, Vavilovian, where a weed is unintentionally artificially selected to resemble a crop plant, Pouyannian, in which a flower imitates a female mate for a pollinating insect, Batesian, where a harmless species deter predators by mimicking the characteristics of a harmful species, and leaf mimicry, where a plant resembles a nearby plant to evade the attention of herbivores.

Bakerian

Bakerian mimicry, named after English naturalist Herbert Baker, [3] is a form of automimicry or intraspecific mimicry that occurs within a single species. In plants, the female flowers mimic male flowers of their own species, cheating pollinators out of a reward. This reproductive mimicry may not be readily apparent as members of the same species may still exhibit some degree of sexual dimorphism, i.e. the phenotypic difference between males and females of the same species. It is common in many species of Caricaceae, a family of flowering plants in the order Brassicales, found primarily in tropical regions of Central and South America, and Africa. [4] [5]

Dodsonian

Dodsonian mimicry, named after American botanist, orchidologist, and taxonomist, Calaway H. Dodson, is a form of reproductive floral mimicry, but the model belongs to a different species than the mimic. [6] By providing similar sensory signals as the model flower, it can lure its pollinators. Like Bakerian mimics, no nectar is provided.

Examples

Epidendrum ibaguense , a species of epiphytic orchid of the genus Epidendrum that occurs in Trinidad, French Guiana, Venezuela, Colombia, and northern Brazil, resembles flowers of Lantana camara and Asclepias curassavica (commonly called Mexican butterfly weed, blood-flower, scarlet milkweed, or tropical milkweed), both are species of flowering plant with the first in the verbena family, while the latter belongs to the milkweed family, and both are native to the American tropics. Epidendrum ibaguense is pollinated by monarch butterfly (Danaus plexippus) and perhaps hummingbirds. [7] Similar cases are seen in some other species of the same family. The mimetic species may still have pollinators of its own though, for example a Lamellicorn beetle, which usually pollinates correspondingly colored Cistus flowers, is also known to aid in pollination of Ophrys species that are normally pollinated by bees. [8]

Vavilovian

Vavilovian mimicry (also known as crop mimicry or weed mimicry [n 1] ), named after Russian plant geneticist who identified the centres of origin of cultivated plants, Nikolai Vavilov, [9] is a form of mimicry in plants where a weed comes to share one or more characteristics with a domesticated plant through generations of artificial selection. [10] Selection against the weed may occur by killing a young or adult weed, separating its seeds from those of the crop (winnowing), or both. This has been done manually since Neolithic times, and in more recent years by agricultural machinery.

Pouyannian

Bee orchid flower resembles a female bee closely enough to attract males in search of a mate Ophrys apifera flower1.jpg
Bee orchid flower resembles a female bee closely enough to attract males in search of a mate

Many plants have evolved to appear like other organisms, most commonly insects. This can have wide-ranging benefits including increasing pollination. In Pouyannian mimicry, [11] flowers mimic a potential female mate visually, but the key stimuli are often chemical and tactile. [12]

Examples

The hammer orchid ( Drakaea spp., an endangered genus of orchid that is native to Australia) is one of the most notable examples. The orchid has both visual and olfactory mimics of a female wasp to lure males to both deposit and pick up pollen. [13] [ better source needed ]

The orchid Epipactis helleborine is physiologically and morphologically adapted to attract social wasps as their primary pollinators. Social wasps feed their larvae on insects like caterpillars. To locate that prey, they use a combination of visual and olfactory cues. The flowers of E. helleborine and E. purpurata emit green-leaf volatiles (GLVs), which are attractive to foragers of the social wasps Vespula germanica and V. vulgaris . Several E. helleborine GLVs that induced a response in the antennae of wasps were also emitted by cabbage leaves infested with caterpillars ( Pieris brassicae), which are common prey items for wasps. Despite a large nectar reward, the species is almost entirely overlooked by other pollinators. [14]

Carrion flowers mimic the scent and appearance of rotting flesh to attract necrophagous (carrion-feeding) insects like flesh flies ( Sarcophagidae ), blowflies ( Calliphoridae ), house flies ( Muscidae ) and some beetles (e.g., Dermestidae and Silphidae ) which search for dead animals to use as brood sites. The decaying smell of the flower comes from oligosulfides, decayed proteins that contain amino acids methionine and cysteine. While carrion flowers do produce a small amount of nectar, this does not necessarily make its relationship to necrophagous insects mutualistic. Insects lay eggs on the carrion flowers, meaning they mistake them for oviposition sites. The nectar acts as a lure to bring the insects closer to the reproductive parts of the flower. [15]

Batesian

In Batesian mimicry, named after the English naturalist Henry Walter Bates, a harmless species has evolved to imitate the warning signals of a harmful species directed at a predator.

Examples

Thorn mimicry of two types has been observed in plants. The first, a special case of intra-organismic Batesian mimicry characteristic of Aloe sp. (Liliaceae), W. filifera (Palmaceae), and dozens of species of Agave, including A. applanta, A. salmiana, and A. obscura. These plants develop thorn-like imprints or colorations on the face of their leaves due to the teeth along the margins of that leaf (or another leaf) pressing sustained indentations into the flesh of the non-spiny parts.

The second type of thorn mimicry, a more classic case of Batesian mimicry, involves the pointed, colorful organs like buds, leaves and fruit of memetic plant species that mimic aposematic colorful thorns not found anywhere else in the organism. [16]

Several plants growing in Israel, Estonia, Greece, and Japan exhibit possible spider web mimicry. Dense, white trichomes are produced on newly extended stems and leaves that deter herbivory due to predatory habit or toxicity. This may be a case of visual mimicry or perceptual exploitation. Case examples include the new buds of Onopordum from Israel, Carthamus sp. from Greece, flower heads of Arctium tomentosum from Estonia, a fledgling leaf of Tussilago farfara from Estonia, and new fronds of Osmunda japonica from Japan. [17]

Cryptic mimicry

In ecology, crypsis is an organism's ability to avoid detection by other organisms. Therefore, cryptic mimicry is a situation where a prey organism deceives a potential predator by providing false signals or a lack of signals. Cryptic mimicry in plants is usually achieved visually.

Examples

Boquila trifoliata , a South American member of the family Lardizabalaceae, is a climbing vine with a highly variable phenotype. It is capable of mimicking the leaf features of plant species that it clings to, adopting color shape and size. By camouflaging its leafy appendages, Boquila lowers its rate of herbivory. [1]

See also

Notes

  1. In this case the weed is the mimic, not the model as in ant mimicry.

Related Research Articles

<span class="mw-page-title-main">Pollinator</span> Animal that moves pollen from the male anther of a flower to the female stigma

A pollinator is an animal that moves pollen from the male anther of a flower to the female stigma of a flower. This helps to bring about fertilization of the ovules in the flower by the male gametes from the pollen grains.

<span class="mw-page-title-main">Hoverfly</span> Family of insects

Hoverflies, also called flower flies or syrphids, make up the insect family Syrphidae. As their common name suggests, they are often seen hovering or nectaring at flowers; the adults of many species feed mainly on nectar and pollen, while the larvae (maggots) eat a wide range of foods. In some species, the larvae are saprotrophs, eating decaying plant and animal matter in the soil or in ponds and streams. In other species, the larvae are insectivores and prey on aphids, thrips, and other plant-sucking insects.

<span class="mw-page-title-main">Mimicry</span> Imitation of another species for selective advantage

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. Often, mimicry functions to protect a species from predators, making it an anti-predator adaptation. Mimicry evolves if a receiver perceives the similarity between a mimic and a model and as a result changes its behaviour in a way that provides a selective advantage to the mimic. The resemblances that evolve in mimicry can be visual, acoustic, chemical, tactile, or electric, or combinations of these sensory modalities. Mimicry may be to the advantage of both organisms that share a resemblance, in which case it is a form of mutualism; or mimicry can be to the detriment of one, making it parasitic or competitive. The evolutionary convergence between groups is driven by the selective action of a signal-receiver or dupe. Birds, for example, use sight to identify palatable insects and butterflies, whilst avoiding the noxious ones. Over time, palatable insects may evolve to resemble noxious ones, making them mimics and the noxious ones models. In the case of mutualism, sometimes both groups are referred to as "co-mimics". It is often thought that models must be more abundant than mimics, but this is not so. Mimicry may involve numerous species; many harmless species such as hoverflies are Batesian mimics of strongly defended species such as wasps, while many such well-defended species form Müllerian mimicry rings, all resembling each other. Mimicry between prey species and their predators often involves three or more species.

<span class="mw-page-title-main">Pseudocopulation</span> Biological process

Pseudocopulation describes behaviors similar to copulation that serve a reproductive function for one or both participants but do not involve actual sexual union between the individuals. It is most generally applied to a pollinator attempting to copulate with a flower. Some flowers mimic a potential female mate visually, but the key stimuli are often chemical and tactile. This form of mimicry in plants is called Pouyannian mimicry.

<span class="mw-page-title-main">Batesian mimicry</span> Bluffing imitation of a strongly defended species

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.

<span class="mw-page-title-main">Entomophily</span> Form of pollination by insects

Entomophily or insect pollination is a form of pollination whereby pollen of plants, especially but not only of flowering plants, is distributed by insects. Flowers pollinated by insects typically advertise themselves with bright colours, sometimes with conspicuous patterns leading to rewards of pollen and nectar; they may also have an attractive scent which in some cases mimics insect pheromones. Insect pollinators such as bees have adaptations for their role, such as lapping or sucking mouthparts to take in nectar, and in some species also pollen baskets on their hind legs. This required the coevolution of insects and flowering plants in the development of pollination behaviour by the insects and pollination mechanisms by the flowers, benefiting both groups. Both the size and the density of a population are known to affect pollination and subsequent reproductive performance.

<i>Ophrys insectifera</i> Species of flowering plant in the orchid family Orchidaceae

Ophrys insectifera, the fly orchid, is a species of orchid and the type species of the genus Ophrys. It is remarkable as an example of the use of sexually deceptive pollination and floral mimicry, as well as a highly selective and highly evolved plant–pollinator relationship.

<i>Drakaea</i> Genus of orchids

Drakaea is a genus of 10 species in the plant family Orchidaceae commonly known as hammer orchids. All ten species only occur in the south-west of Western Australia. Hammer orchids are characterised by an insectoid labellum that is attached to a narrow, hinged stem, which holds it aloft. The stem can only hinge backwards, where the broadly winged column carries the pollen and stigma. Each species of hammer orchid is pollinated by a specific species of thynnid wasp. Thynnid wasps are unusual in that the female is flightless and mating occurs when the male carries a female away to a source of food. The labellum of the orchid resembles a female thynnid wasp in shape, colour and scent. Insect pollination involving sexual attraction is common in orchids but the interaction between the male thynnid wasp and the hammer orchid is unique in that it involves the insect trying to fly away with a part of the flower.

Sexual mimicry occurs when one sex mimics the opposite sex in its behavior, appearance, or chemical signalling.

<i>Hymenopus coronatus</i> Species of praying mantis

Hymenopus coronatus is a mantis from the tropical forests of Southeast Asia. It is known by various common names, including walking flower mantis, orchid-blossom mantid and (pink) orchid mantis. It is one of several species known as flower mantids, a reference to their unique physical form and behaviour, which often involves moving with a “swaying” motion, as if being “blown” in the breeze. Several species have evolved to mimic orchid flowers as a hunting and camouflaging strategy, “hiding” themselves in plain view and preying upon pollinating insects that visit the blooms. They are known to grab their prey with blinding speed.

<span class="mw-page-title-main">Ant mimicry</span> Animals that resemble ants

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.

<span class="mw-page-title-main">Flower mantis</span> Species of mantis camouflaged to resemble flowers to lure their prey

Flower mantises are praying mantises that use a special form of camouflage referred to as aggressive mimicry, which they not only use to attract prey, but avoid predators as well. These insects have specific colorations and behaviors that mimic flowers in their surrounding habitats.

<span class="mw-page-title-main">Aggressive mimicry</span> Deceptive mimicry of a harmless species by a predator

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.

<span class="mw-page-title-main">Insect ecology</span> The study of how insects interact with the surrounding environment

Insect ecology is the interaction of insects, individually or as a community, with the surrounding environment or ecosystem.

<span class="mw-page-title-main">Wasp</span> Group of insects

A wasp is any insect of the narrow-waisted suborder Apocrita of the order Hymenoptera which is neither a bee nor an ant; this excludes the broad-waisted sawflies (Symphyta), which look somewhat like wasps, but are in a separate suborder. The wasps do not constitute a clade, a complete natural group with a single ancestor, as bees and ants are deeply nested within the wasps, having evolved from wasp ancestors. Wasps that are members of the clade Aculeata can sting their prey.

<span class="mw-page-title-main">Chemical mimicry</span> Biological mimicry using chemicals

Chemical mimicry is a type of biological mimicry involving the use of chemicals to dupe an operator.

Diptera is an order of winged insects commonly known as flies. Diptera, which are one of the most successful groups of organisms on Earth, are very diverse biologically. None are truly marine but they occupy virtually every terrestrial niche. Many have co-evolved in association with plants and animals. The Diptera are a very significant group in the decomposition and degeneration of plant and animal matter, are instrumental in the breakdown and release of nutrients back into the soil, and whose larvae supplement the diet of higher agrarian organisms. They are also an important component in food chains.

<i>Argogorytes mystaceus</i> Species of wasp

Argogorytes mystaceus is a species of solitary wasp in the family Crabronidae.

<span class="mw-page-title-main">Chemical communication in insects</span>

Chemical communication in insects is social signalling between insects of the same or different species, using chemicals. These chemicals may be volatile, to be detected at a distance by other insects' sense of smell, or non-volatile, to be detected on an insect's cuticle by other insects' sense of taste. Many of these chemicals are pheromones, acting like hormones outside the body.

<span class="mw-page-title-main">Pollination of orchids</span>

The pollination of orchids is a complex chapter in the biology of this family of plants that are distinguished by the complexity of their flowers and by intricate ecological interactions with their pollinator agents. It has captured the attention of numerous scientists over time, including Charles Darwin, father of the theory of evolution by natural selection. Darwin published in 1862 the first observations of the fundamental role of insects in orchid pollination, in his book The Fertilization of Orchids. Darwin stated that the varied stratagems orchids use to attract their pollinators transcend the imagination of any human being.

References

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  11. Pasteur 1982, p. 169.
  12. van der Pijl & Dodson 1966, pp. 129–141.
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