The Adaptive Significance of Batesian Mimicry in the Swallowtail Butterfly,Papilio polytes (Insecta,Papilionidae): Associative Learning in a Predator

Experiments were conducted to examine the adaptive significance of Batesian mimicry in the swallowtail butterfly, Papilio polytes, with its model, Pacbliopta aristolochiae, an alkaloidal butterfly. The female of Pap. polytes is polymorphic, whereas the male is monomorphic. Two forms of the female, f. polytes mimic and f. cyrus non-mimic, were used in these experiments. Naive birds, brown-eared bulbuls Hypsipetes amaurotis pryeri, were trained to take food from two feeders in captivity, and then were offered Pach. aristolochiae in one of the feeders. After experiencing an uncomfortable encounter with this species, the birds reduced the frequency of taking regular food from the feeder where the butterfly had been placed. This result suggests that the birds can learn not only the model itself but also the place where they have experienced it. Thereafter, the birds also came to avoid the mimetic form of f. polytes. It is suspected that wild predators behave in the same way. These findings imply that it is adaptive for the mimic to overlap its habitats and daily activity with those of the model species.     

蝶类的拟态现象

拟态是一物种在形态、色型和行为上模拟另一物种,从而获得好处的行为,拟态可区分为贝次拟态、缪勒拟态和拟态集团3种类型。以蝶类为例介绍了这3种拟态的概念和实例,并论述了拟态现象的进化过程。     

Evolvability and robustness in a complex signalling circuit

Biological systems at various levels of organisation exhibit robustness, as well as phenotypic variability or evolvability, the ability to evolve novel phenotypes. We still know very little about the relationship between robustness and phenotypic variability at levels of organisation beyond individual macromolecules, and especially for signalling circuits. Here, we examine multiple alternate topologies of the Saccharomyces cerevisiae target-of-rapamycin (TOR) signalling circuit, in order to understand the circuit's robustness and phenotypic variability. We consider each of the topological variants a genotype, a set of alternative interactions between TOR circuit components. Two genotypes are neighbours in genotype space if they can be reached from each other by a single small genetic change. Each genotype (topology) has a signalling phenotype, which we define via the concentration trajectories of key signalling molecules. We find that the circuits we study can produce almost 300 different phenotypes. The number of genotypes with a given phenotype varies very widely among these phenotypes. Some phenotypes have few associated genotypes. Others have many genotypes that form genotype networks extending far through genotype space. A minority of phenotypes accounts for the vast majority of genotypes. Importantly, we find that these phenotypes tend to have large genotype networks, greater robustness and a greater ability to produce novel phenotypes. Thus, over a broad range of phenotypic robustness, robustness facilitates phenotypic variability in our study system. Our observations show parallels to studies on macromolecules, suggesting that similar principles might govern robustness and phenotypic variability in biological systems. Our approach points a way towards mapping genotype spaces in complex circuitry, and it exposes some challenges such mapping faces.     

Once a Batesian mimic, not always a Batesian mimic: mimic reverts back to ancestral phenotype when the model is absent

Batesian mimics gain protection from predation through the evolution of physical similarities to a model species that possesses anti-predator defences. This protection should not be effective in the absence of the model since the predator does not identify the mimic as potentially dangerous and both the model and the mimic are highly conspicuous. Thus, Batesian mimics should probably encounter strong predation pressure outside the geographical range of the model species. There are several documented examples of Batesian mimics occurring in locations without their models, but the evolutionary responses remain largely unidentified. A mimetic species has four alternative evolutionary responses to the loss of model presence. If predation is weak, it could maintain its mimetic signal. If predation is intense, it is widely presumed the mimic will go extinct. However, the mimic could also evolve a new colour pattern to mimic another model species or it could revert back to its ancestral, less conspicuous phenotype. We used molecular phylogenetic approaches to reconstruct and test the evolution of mimicry in the North American admiral butterflies (Limenitis: Nymphalidae). We confirmed that the more cryptic white-banded form is the ancestral phenotype of North American admiral butterflies. However, one species, Limenitis arthemis, evolved the black pipevine swallowtail mimetic form but later reverted to the white-banded more cryptic ancestral form. This character reversion is strongly correlated with the geographical absence of the model species and its host plant, but not the host plant distribution of L. arthemis. Our results support the prediction that a Batesian mimic does not persist in locations without its model, but it does not go extinct either. The mimic can revert back to its ancestral, less conspicuous form and persist.     

The Structure of Autocatalytic Sets: Evolvability, Enablement, and Emergence

This paper presents new results from a detailed study of the structure of autocatalytic sets. We show how autocatalytic sets can be decomposed into smaller autocatalytic subsets, and how these subsets can be identified and classified. We then argue how this has important consequences for the evolvability, enablement, and emergence of autocatalytic sets. We end with some speculation on how all this might lead to a generalized theory of autocatalytic sets, which could possibly be applied to entire ecologies or even economies.     

Playing God,Playing Adam: The Politics and Ethics of Enhancement

The question of enhancement occupies a prominent place not only in current bioethical debates but also in wider public discussions about our human future. In all of these, the problem of enhancement is usually articulated via two sets of questions: moral questions over its permissibility, extent and direction; and technical questions over the feasibility of different forms of regenerative and synthetic alterations to human bodies and minds. This article argues that none of the dominant positions on enhancement within the field of bioethics is entirely satisfactory due to the limited, monadic, pre-technological and non-cultural conception of the human that is adopted in these models. Critically engaging with both opponents of enhancement (Habermas) and its advocates (Harris, Agar, Bostrom, Dworkin), Zylinska also takes some steps towards outlining a nonnormative ethics of enhancement. The latter sees its human and non-human subjects as always already enhanced, and hence dependent, relational and coevolving with technology.     

"Playing between Classes": America's Troubles with Class, Race, and Gender in a Black High School and Community

A cultural and relational framework of social class is used to present an ethnographic portrait of class as it unfolds with race and gender in a black high school and community. Traditionally viewed as troubling, these students (and staff) play between classes in ways that impact structural analyses of class and their implications for public policy.     

Playing with Culture: The Serious Side of Humor

Indi'n Humor: Bicultural Play in Native America . Kenneth Lincoln
Keeping Slug Woman Alive: A Holistic Approach to American Indian Texts . Greg Sarris     

The Evolution of Canalization and Evolvability in Stable and Fluctuating Environments

Using a multilinear model of epistasis we explore the evolution of canalization (reduced mutational effects) and evolvability (levels of additive genetic variance) under different forms of stabilizing and fluctuating selection. We show that the total selection acting on an allele can be divided into a component deriving from adaptation of the trait mean, a component of canalizing selection favoring alleles that epistatically reduce the effects of other allele substitutions, and a component of conservative selection disfavoring rare alleles. While canalizing selection operates in both stable and fluctuating environments, it may not typically maximize canalization, because it gets less efficient with increasing canalization, and reaches a balance with drift, mutation and indirect selection. Fluctuating selection leads to less canalized equilibria than stabilizing selection of comparable strength, because canalization then becomes influenced by erratic correlated responses to shifting trait adaptation. We conclude that epistatic systems under bounded fluctuating selection will become less canalized than under stabilizing selection and may support moderately increased evolvability if the amplitude of fluctuations is large, but canalization is still stronger and evolvability lower than expected under neutral evolution or under patterns of selection that shift the trait in directions of positive (reinforcing) epistasis.     

Conditional use of honest signaling by a Batesian mimic

Jumping spiders (Salticidae) usually avoid ants, but some specieswithin this family single out ants as preferred prey, whileothers (especially the species in the genus Myrmarachne) areBatesian mimics of ants. Field records show that ant-eatingsalticids sometimes prey on Myrmarachne, suggesting that theunwanted attention of predators that specialize on the modelmay be an important, but poorly understood, cost of Batesianmimicry. By staging encounters in the laboratory between livingant-eating salticids and Myrmarachne, we determined that ant-eatingsalticids attack Myrmarachne. However, when Myrmarachne detectsa stalking ant-eating salticid early enough, it adopts a distinctivedisplay posture (legs almost fully extended, elevated 45°,and held out to the side 45°), and this usually deters thepredator. When Myrmarachne detects an ant-eating salticid beforestalking begins, Myrmarachne makes preemptive displays thatappear to inhibit the initiation of stalking. Using immobilelures made from dead Myrmarachne that were either in a displayposture or a nondisplay posture, we ascertained that specificallythe display posture of Myrmarachne deters the initiation ofstalking (ant-eating salticids stalked nondisplaying more oftenthan displaying lures). In another experiment, we ascertainedthat it is specifically the interjection of display posturethat deters stalking. When ant-eating salticids that had alreadybegun stalking experienced lures that switched from a nondisplayto a display posture, they stopped stalking. Although the unwantedattentions of its models' predators may be, for Myrmarachne,a hidden cost of Batesian mimicry, Myrmarachne appears to havean effective defense against these predators.     

Comparing Evolvability and Variability of Quantitative Traits

There are two distinct reasons for making comparisons of genetic variation for quantitative characters. The first is to compare evolvabilities, or ability to respond to selection, and the second is to make inferences about the forces that maintain genetic variability. Measures of variation that are standardized by the trait mean, such as the additive genetic coefficient of variation, are appropriate for both purposes. Variation has usually been compared as narrow sense heritabilities, but this is almost always an inappropriate comparative measure of evolvability and variability. Coefficients of variation were calculated from 842 estimates of trait means, variances and heritabilities in the literature. Traits closely related to fitness have higher additive genetic and nongenetic variability by the coefficient of variation criterion than characters under weak selection. This is the reverse of the accepted conclusion based on comparisons of heritability. The low heritability of fitness components is best explained by their high residual variation. The high additive genetic and residual variability of fitness traits might be explained by the great number of genetic and environmental events they are affected by, or by a lack of stabilizing selection to reduce their phenotypic variance. Over one-third of the quantitative genetics papers reviewed did not report trait means or variances. Researchers should always report these statistics, so that measures of variation appropriate to a variety of situations may be calculated.