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#Batesian mimicry

13 public questions tagged with this topic.

The mimic and model resemble each other but are unrelated due to:

Resemblance between unrelated model and mimic is an example of convergent evolution produced by selective advantage, not shared ancestry or gene flow. Individuals in the mimic population that more closely match a signal already avoided by predators survive and reproduce at higher rates. Across generations, selection increases alleles affecting color, shape, movement, odor, or other relevant traits, even though the model belongs to a separate lineage. Habitat sharing can create the ecological opportunity because both organisms encounter the same receivers, but proximity alone does not generate

Ref: Evolutionary Analysis, Herron & Freeman, 5th Ed., Ch. 10

Which of these is *not* a mimicry type?

Mertensian, Wasmannian, and Batesian are recognized terms for distinct forms of mimicry, whereas “transitive mimicry” is not a standard biological category. Mertensian mimicry proposes that a highly dangerous species converges on the warning pattern of a less dangerous species because predators cannot learn from fatal encounters with the most dangerous form. Wasmannian mimicry involves guests or parasites resembling social insects in whose colonies they live. Batesian mimicry occurs when an undefended or palatable organism gains protection by resembling a defended, avoided model. These labels

Ref: Evolutionary Analysis, Herron & Freeman, 5th Ed., Ch. 10

Bright coloration and bad taste together are indicative of:

Bright coloration coupled with an unpleasant taste is the characteristic combination underlying aposematism. A defended animal advertises its low profitability through a conspicuous signal, and predators learn after one or a few adverse encounters to avoid similarly patterned prey. The bad taste supplies the reinforcing cost; the bright pattern improves detection, recognition, and memory. This may initially seem paradoxical because conspicuous prey are easier to locate, but once avoidance develops, the reduction in repeated attacks can exceed the cost of occasional predator education. Aggregat

Ref: Evolutionary Analysis, Herron & Freeman, 5th Ed., Ch. 10

A harmless fish resembling a venomous one shows:

A harmless fish that resembles a venomous fish gains protection without producing the costly defense itself, which is the defining asymmetry of Batesian mimicry. Predators that have been injured by, or have learned to avoid, the venomous model generalize its recognizable shape, coloration, or behavior to the edible mimic. The mimic benefits because mistaken identity lowers attack probability, while excessive mimic abundance can disadvantage the model by making its warning signal less reliable. This contrasts with Müllerian mimicry, where both resembling species are defended and share the cost

Ref: Evolutionary Analysis, Herron & Freeman, 5th Ed., Ch. 10

Which mimicry is most likely used by a beetle living among ants and mimicking their appearance?

Wasmannian mimicry describes organisms that resemble the social insects within whose nests or colonies they live. Numerous beetles, flies, mites, and other myrmecophiles imitate ant body shape, coloration, movement, or chemical odor, allowing them to avoid aggression and gain access to shelter, food, or brood. Visual resemblance alone may be insufficient because ants rely strongly on cuticular hydrocarbons; some associates biosynthesize, acquire, or otherwise imitate the colony’s recognition chemicals. This colony-associated deception distinguishes Wasmannian mimicry from Batesian mimicry, in

Ref: Evolutionary Analysis, Herron & Freeman, 5th Ed., Ch. 10

Which is *not* a condition for successful Batesian mimicry?

Successful Batesian mimicry usually requires the harmless mimic to remain less common than the harmful or unpalatable model. Predators learn the shared warning phenotype by sampling organisms and experiencing the model’s defense. If harmless mimics become too abundant, attacks on that phenotype are rewarded too often, avoidance weakens, and the protective value of resemblance declines through negative frequency-dependent selection. An educated predator is therefore important, because learned association links the model’s appearance with danger. The model normally needs to outnumber the mimic,

Ref: Evolutionary Analysis, Herron & Freeman, 5th Ed., Ch. 10

Mimicry involving no learning opportunity for predator due to prey lethality leads to:

Mertensian mimicry addresses the learning problem created by extremely lethal prey. A predator killed during its first sampling event cannot retain or transmit learned avoidance through its own later choices. The hypothesis proposes that a deadly species gains protection by resembling a less dangerous but still noxious model that predators can sample, survive, and learn to avoid. The shared appearance then protects the lethal mimic without requiring direct education by fatal encounters. Batesian mimicry involves a harmless mimic, Müllerian mimicry involves mutually defended species reinforcing

Ref: Evolutionary Analysis, Herron & Freeman, 5th Ed., Ch. 10

King snake mimicking coral snake is an example of:

A nonvenomous king snake can resemble a venomous coral snake in its conspicuous ringed coloration. Predators that avoid coral snakes may generalize that response to the harmless look-alike, allowing the king snake to gain protection without producing venom. This is the classic logic of Batesian mimicry: an undefended mimic copies a defended model. Müllerian mimicry would require both species to impose meaningful costs on predators, Wasmannian mimicry concerns close associates of social insects, and Mertensian mimicry involves an extremely lethal form resembling a less dangerous defended model.

Ref: Evolutionary Analysis, Herron & Freeman, 5th Ed., Ch. 10

Mertensian mimicry involves:

Mertensian, or Emsleyan, mimicry proposes that an extremely dangerous or lethal species resembles a less harmful but still defended species. A predator may survive an encounter with the moderately harmful model and learn to avoid its warning pattern, then also avoid the deadly mimic. If the predator's first encounter with the lethal species caused death, that individual could not learn, so selection for an educational signal would be difficult to explain directly. This arrangement differs from Batesian mimicry, where a harmless form copies a defended one, and Müllerian mimicry, where defended

Ref: Evolutionary Analysis, Herron & Freeman, 5th Ed., Ch. 10

What kind of mimicry does a hoverfly show by resembling a wasp?

Hoverflies possess no sting, yet many display yellow-and-black banding, body shapes, and flight behavior resembling wasps. Predators that have learned to avoid stinging hymenopterans may also avoid these edible flies, giving the hoverfly protection without the cost of venom or a sting apparatus. This is Batesian mimicry, in which an undefended mimic copies a defended model. Müllerian mimicry requires both participants to be defended, aggressive mimicry helps a predator or parasite approach a victim, and Wasmannian mimicry concerns organisms resembling hosts or associates within social-insect c

Ref: Evolutionary Analysis, Herron & Freeman, 5th Ed., Ch. 10

The mimic in Batesian mimicry is:

A Batesian mimic lacks the costly defense of the model but resembles its warning signal. A harmless hoverfly, for example, may gain protection by resembling a stinging wasp, because experienced predators generalize avoidance from model to mimic. The mimic benefits while the model can be disadvantaged if edible mimics make the signal less reliable. When both similar species are genuinely defended, the system is Müllerian rather than Batesian. Being merely distasteful would itself constitute a defense and would not match the defining harmless-mimic relationship. The evolutionary advantage depend

Ref: Evolutionary Analysis, Herron & Freeman, 5th Ed., Ch. 10