Manipulating badges of status only fools strangers

Conflict is risky, but mechanisms that allow animals to assess dominance status without aggression can reduce such costs. Two different mechanisms of competitor assessment are expected to evolve in different contexts: badges of status are expected in larger, anonymous groups, whereas individual recognition is feasible in small, stable groups. However, both mechanisms may be important when social interactions occur both within and across stable social groups. We manipulated plumage in golden‐crowned sparrows (Zonotrichia atricapilla) and found that two known badges of status – gold and black head plumage patch sizes – independently affect dominance among strangers but manipulations had no effect on dominance among familiar flockmates. Moreover, familiar flockmates showed less aggression and increased foraging relative to strangers. Our study provides clear experimental evidence that social recognition affects badge function, and suggests that variation in social contexts maintains coexistence and context‐dependent use of these two dominance resolution mechanisms.     

Mimicry: Status of a classical evolutionary paradigm

Accounts of mimetic relationships reflect the traditional enthusiasm with which protective adaptations are described. However, our understanding of mimicry remains largely untested. Recent reviews of mimicry embrace many diverse phenomena, from tactics for defence and foraging, to pollination and mating. Selection for these mimetic phenomena is very different in each case and it is important to distinguish among categories of trophic, interspecific mimicry and sexually selected, nontrophic, intraspecific mimicry. Once categories are distinguished, the diversity of selection should clarify misunderstood concepts, such as the 'Batesian-Mallerian mimicry spectrum'. Experimental evidence of the selective value of mimicry is needed so that the advantages to mimics are clear when mimetic prey are confronted with real predator diversity. Such evidence should clarify the debate on how aposematism and mimicry evolve.     

Ecological and Evolutionary Processes Drive the Origin and Maintenance of Imperfect Mimicry

Although the forces behind the evolution of imperfect mimicry remain poorly studied, recent hypotheses suggest that relaxed selection on small-bodied individuals leads to imperfect mimicry. While evolutionary history undoubtedly affects the development of imperfect mimicry, ecological community context has largely been ignored and may be an important driver of imperfect mimicry. Here we investigate how evolutionary and ecological contexts might influence mimetic fidelity in Müllerian and Batesian mimicry systems. In Batesian hoverfly systems we find that body size is not a strong predictor of mimetic fidelity. However, in Müllerian velvet ants we find a weak positive relationship between body size and mimetic fidelity when evolutionary context is controlled for and a much stronger relationship between community diversity and mimetic fidelity. These results suggest that reduced selection on small-bodied individuals may not be a major driver of the evolution of imperfect mimicry and that other factors, such as ecological community context, should be considered when studying the evolution of imperfect mimicry.     

Status signalling and the ability to recognize dominants: an experiment with siskins (Carduelis spinus)

Because dominants usually exploit others and take a disproportionate share of the available resources, we should expect foragers to be choosy as to which individuals they join. Here we show that siskins (Carduelis spinus) discriminate between dominant and subordinate individuals on the first encounter without requiring cues such as overt aggression, and prefer to join subordinate individuals. Experimental enlargement or removal of the siskin black bib, which has been shown previously to be a reliable predictor of dominance, strongly suggests that dominance discrimination is based on the use of badges of status.     

Rejection of Conspecific Eggs in Chaffinches: The Effect of Age and Clutch Characteristics

Previous experimental studies have found that the majority of chaffinches, Fringilla coelebs, are able to reject both non‐mimetic and mimetic cuckoo eggs and also non‐mimetic conspecific eggs. However, interestingly the frequency of rejecters of moderately mimetic conspecific eggs has been found to be only approx. 50%. We examined the possibility that acceptors of moderately mimetic conspecific eggs are first time breeders, because these individuals may lack the experience needed to reject eggs that deviate only slightly from their own eggs. Older individuals, with good knowledge of their own egg appearance, should therefore reject such eggs. We also examined the possibility that acceptors of moderately mimetic eggs have a higher intraclutch variation in egg appearance, which makes it more difficult to recognize such eggs when compared with rejecters. We obtained no support for any age‐specific pattern in rejection behaviour. Furthermore, there was no relationship between age and intraclutch variation, or intraclutch variation and rejection behaviour. As there is no evidence of intraspecific brood parasitism in this species, the rejection of any foreign eggs is most probably an adaptation to past cuckoo, Cuculus canorus, parasitism. Acceptance of good and moderately mimetic conspecific eggs is probably due to cognitive limitations, because evolution of a more fine‐tuned recognition ability is unnecessary in the absence of intraspecific brood parasitism.     

Visual signals of status and rival assessment in Polistes dominulus paper wasps

Aggressive competition is an important aspect of social interactions, but conflict can be costly. Some animals are thought to minimize the costs of conflict by using conventional signals of agonistic ability (i.e. badges of status) to assess rivals. Although putative badges have been found in a range of taxa, little research has tested whether individuals use badges to assess potential rivals before they engage in aggressive contests. Here, choice trials were used to test how the variable black facial patterns in Polistes dominulus wasps are used during rival assessment. Focal wasps were given access to two patches of food, each guarded by a wasp whose facial pattern had been experimentally altered. Wasps chose food patches based on the facial pattern of the guard, preferring to challenge guards with facial patterns indicating a low level of quality, while avoiding guards with facial patterns indicating a high level of quality. Therefore, status badges play an important role during rival assessment; paper wasps use facial patterns alone to quickly assess the agonistic abilities of strangers.     

BADGE SIZE,PHENOTYPIC QUALITY,AND REPRODUCTIVE SUCCESS IN THE HOUSE SPARROW: A STUDY ON HONEST ADVERTISEMENT

Honest signaling theory suggests that advertising traits must be costly to their bearer; thus, only individuals of high phenotypic quality can exhibit maximal expression of these traits. Males of the sexually dichromatic house sparrow, Passer domesticus, have a black throat patch that functions as a badge of status. I investigated whether badge size honestly shows phenotypic quality. Badge size increases with age and decreases with advancing fledging date in yearling males; thus, badge size was larger in older individuals even though age differences were small. Badge size also increased with physical condition independent of age. These results indicate that badge size functions as an honest signal, possibly because there are costs involved in its production. I also found that males with enlarged badges acquired more nest sites than either control males or males with reduced badges. However, males with enlarged badges possessing a nest site raised fewer fledglings per year than did males with reduced badges, suggesting that cheating has no selective benefit. Further studies that accurately measure the energy expenditure allocated to badge production and that quantify additional fitness components are needed to clarify how reliable badges are maintained.     

Some problems of the study and representation of Siberian flora biodiversity in connection with its conservation

The present knowledge of flora of Siberia is quite insufficient, which is a considerable obstacle to the detection of its biodiversity for conserving the gene pool. Planning conservation measures should be focused not only on species, but also on intraspecific taxa and their phylogenetic uniqueness. In the absence of genetic data, available morphological and geographical methods should be used, so that, when it is impossible to establish the actual origin and relationship of taxa, the existing morphological diverstity is at least represented, as far as it is known to be based on genetic diversity. Phenetic maps can be of much use in the study of intraspecific morphological diversity. The estimation of geographic variability and morphological diversity, as well as the evaluation of territories, can be based on such maps. To represent adequately the biodiversity existing within poorly studied, presumably hybrid plant groups, until actual origin and relationship are known, they should probably be forcedly and provisionally considered as a special type of hybrid complexes, representing the unclear present day taxonomic situation. Such complexes could include populations and individuals with morphological characters of two or more different species, until the systematic position of such populations and individuals is further explored. Until the actual taxonomic status and relationship of the components are established, they could be regarded as subspecies permitted by the Code, or as certain recorded morphological deviations from the type, without assigning any taxonomic status to them--depending on the available data on variability and distribution. In the future, the resulting provisional information on morphological diversity would help to concentrate the efforts of biologists, in possession of the newest methods, on the most important objects, and serve as the scientific base for effective measures aimed at the conservation and management of the vast gene pool of the Siberian flora.     

Heterospecific female mimicry in Ficedula flycatchers

Mimicry is a widespread phenomenon. Vertebrate visual mimicry often operates in an intraspecific sexual context, with some males resembling conspecific females. Pied flycatcher (Ficedula hypoleuca) dorsal plumage varies from the ancestral black to female‐like brown. Experimental studies have shown that conspecific and heterospecific (collared flycatcher, F. albicollis) individuals of both sexes respond, at least initially, to brown individuals as if they were female. We quantified the perceptual and biochemical differences between brown feathers and found that brown pied flycatcher males are indistinguishable from heterospecific, but not from conspecific, females in both aspects. To our knowledge, this is the first evidence of a visual mimetic signalling system in a sexual context where the model is heterospecific to the mimic. By only mimicking heterospecific females, brown pied flycatcher males can establish territories next to the more dominant collared flycatcher in sympatry, suffer less aggression by darker conspecifics in allopatry and preserve within‐species sexual recognition throughout the breeding range. A closer look at the evolutionary history and ecology of these two species illustrates how such a mimetic system can evolve. Although likely rare, this phenomenon might not be unique to Ficedula flycatchers.     

Sensory discrimination and the incipient advantage of mutations

Perception follows logarithmic or power functions, rather than linear functions, of stimulus intensity. A small increment in stimulus strength can be sufficient to elicit discrimination between individuals of different phenotypes when the initial stimulus magnitude is near zero. This may confer an incipient advantage to the mutation that caused it. The psychophysics of signal receivers may be a good predictor of the extent of phenotypic changes. For example, slight similarities in color of Batesian mimics to their distasteful model can be sufficient to cause predators to reject the mimics. Color changes produced by single mutations in incipient Batesian mimics should be more extensive in mimicry complexes where the predators are less sensitive to color differences.     

Males in seemingly female‐like plumage do not mimic females: UV reflectance reveals temporal cryptic dimorphism in a manakin species exhibiting delayed plumage maturation

Manakins (Pipridae) are neotropical birds that usually exhibit delayed plumage maturation (DPM). Thus, while plumage of most adult male manakins is brightly conspicuous, subadult males and females are basically dull‐olive green. Although sexual dichromatism in some bird species may be evident only through UV reflectance, this phenomenon, known as hidden sexual dichromatism, has not been previously studied in manakins to compare subadult males and females. Within this framework, we carried out spectrophotometric analyses in searching for hidden sexual dichromatism in the white‐bearded manakin Manacus manacus, through comparison of UV spectra in females and subadult males in green plumage. Our results revealed UV reflectance in both sexes in green plumage. Moreover, we found UV spectral differences in homologous color patches between sexes, particularly at belly. Since the observed differences may allow intraspecific sex recognition of individuals in green plumage, our results do not support the female‐mimicry hypothesis to explain delayed plumage maturation in the white‐bearded manakin. Although our findings dismiss the female mimicry hypothesis, we cannot state whether these results support the non‐mutually exclusive cryptic and status signaling hypotheses. We propose then, that dull coloration of subadult males may serve both as a cryptic trait and to limit the energetic costs of acquiring the adult plumage before sexual maturity. Meanwhile, differential UV color traits between sexes in green plumage may allow adult males to avoid unnecessary energy expenditures in courtship displays in the presence of males near leks, and to selectively focus their the courtship displays on females. In accordance with the status signaling hypothesis, subadult males can be recognized both as males and subordinates and consequently may practice courtship displays without suffering aggressions by adult males. Our results highlight the importance to include a wider range of spectrophotometric information analyses for testing hypotheses regarding delayed plumage maturation.     

Obligate brood parasites as selective agents for evolution of egg appearance in passerine birds

Many passerine host species have counteracted the parasite egg mimicry in their coevolutionary arms race with the common cuckoo (Cuculus canorus) by evolving increased interclutch and reduced intraclutch variation in egg appearance. Such variations make it easier for hosts to recognize a foreign egg, reduce the possibility of making recognition errors, and reduce the ability of the cuckoo to mimic the eggs of a particular host. Here, we investigate if such clutch characteristics have evolved among North American passerines. We predict that due to the absence of brood parasites with egg mimicry on this continent, these passerines should (1) not show any relationship between rejection rates and intra- or interclutch variation, and (2) intraclutch variation should be lower and interclutch variation higher in European hosts exposed to cuckoo parasitism as compared to North American hosts parasitized by cowbirds. Here we present data that show support for most of these and other predictions, as well as when controlling statistically for effects of common descent. However, the effect of continent on intraclutch variation was less than predicted and we discuss a possible reason for this. All things considered, the results demonstrate that parasitism by a specialist brood parasite with egg mimicry is a powerful selective force regarding the evolution of egg characteristics in passerine birds.     

Unraveling the relative contribution of inter‐ and intrapopulation functional variability in wild populations of a tadpole species

Functional traits are increasingly recognized as an integrative approach by ecologists to quantify a key facet of biodiversity. And these traits are primarily expressed as species means in previous studies, based on the assumption that the effects of intraspecific variability can be overridden by interspecific variability when studying functional ecology at the community level. However, given that intraspecific variability could also have important effects on community dynamics and ecosystem functioning, empirical studies are needed to investigate the importance of intraspecific variability in functional traits. In this study, 256 Scutiger boulengeri tadpole individuals from four different populations are used to quantify the functional difference between populations within a species, and the relative contribution of inter‐ and intrapopulation variability in functional traits. Our results demonstrate that these four populations differ significantly in functional attributes (i.e., functional position, functional richness, and low functional overlap), indicating that individuals from different populations within a species should be explicitly accounted for in functional studies. We also find similar relative contribution of inter‐ (~56%) and intrapopulation (~44%) variation to the total variability between individuals, providing evidence that individuals within populations should also be incorporated in functional studies. Overall, our results support the recent claims that intraspecific variability cannot be ignored, as well as the general idea of “individual level” research in functional ecology.     

Vocal mimicry in spotted bowerbirds is associated with an alarming context

Although the presence of vocal mimicry in songbirds is well documented, the function of such impressive copying is poorly understood. One explanation for mimicry in species that predominantly mimic alarm calls and predator vocal isations is that these birds use mimicry to confuse or deter potential threats or intruders, so these vocalisations should therefore be produced when the mimic is alarmed and be uncommon in other contexts. Male bowerbirds construct bowers to display to females and anecdotal reports from the Ptilonorhynchus genus suggest that males mimic alarm sounds when disturbed at their bowers. We quantified and compared the rate of mimicry during disturbance to the bower by a human and in naturally occurring social contexts in a population of spotted bowerbirds Ptilonorhynchus maculatus. Male bowerbirds produced mimicry more than thirty times more frequently in response to bower disturbance than they did in any other context. Neither conspecifics nor heterospecifics were attracted to the bower area by mimicry. These data are consistent with the hypothesis that the production of mimicry is associated with a response to an alarming situation. Additionally, the predominance of alarm mimicry by spotted bowerbirds raises the possibility that the birds learn these sounds when they experience alarming situations and they reproduce them in subsequent alarming situations.     

Oxidative damage in relation to a female plumage badge: evidence for signalling costs

Badges of status may be controlled by costs derived from increased aggression from dominant individuals. This cost could be translated into elevated metabolic levels and a concomitant disruption of oxidative balance. Some females in Iberian pied flycatcher Ficedula hypoleuca populations exhibit a white forehead patch similar to that exhibited by all males in this species, functioning in aggressive interactions between females when competing for breeding sites. To test if social stress imposes costs on signalling, we painted white patches on females without natural patches (NP) and compared them with females with natural control (NU). We also over-painted the natural patch in other females (FP) and compared to females with control natural patches (FU). We obtained for the whole sample of females data on reproductive investment, morphology and oxidative damage measured by blood malondialdehydes (MDA), and in a subsample of females variables related to parental care during incubation and the early nestling stage. FP and FU did not differ significantly in any variable which negates an effect of paint itself. However, NP females showed significant higher levels of MDA than NU females when controlling for breeding success for the whole sample, and for female incubation attendance for the parental care subsample. When including the four treatments, there was a significant interaction between the paint treatment and the presence/absence of badges before the experiment when controlling for the significant negative effect of incubation attendance on MDA. Addition of a badge to females without one leads to increased oxidative damage possibly mediated by social control. Badges of status in female pied flycatchers may operate as badges of oxidative status.     

Social Control and Physiological Cost of Cheating in Status Signalling Male House Sparrows (Passer domesticus)

Flock-forming passerines often use plumage characteristics to signal their social dominance. While the benefits to signal dominance seem obvious, costs associated with status signalling are ambiguous. The social control hypothesis predicts that individuals of high social status – with large badges – are involved in more social interactions with individuals of similar badge size. Cheaters are therefore exposed to increased risk of fighting with high quality individuals and the costs associated with enhanced fights with dominant males are supposed to outweigh the benefits of cheating. We tested the social control hypothesis in male house sparrows ( Passer domesticus ), by observing social interactions in captive flocks and determining dominance relationships. Two low status individuals within each flock had the size of their badge experimentally increased and the interactions involving experimental and control birds were recorded. We also assessed the potential physiological cost of cheating in terms of enhanced levels of the stress hormone, corticosterone. Dominance was significantly positively correlated with badge size, but not with other morphological traits. We found little support for the social control hypothesis. Birds did not have significantly more interactions with individuals of similar badge size, before the manipulation. Similarly, after the experimental increase in badge size, experimental birds did not tend to have more encounters with large-badged males. Experimental birds with enlarged badges won more fights compared with prior to the manipulation, suggesting that badge size is used as a signal of social dominance even in small and stable flocks. Finally, corticosterone levels in the blood did not increase significantly after the manipulation of badge size, suggesting that there is no measurable cost, resulting from stress, in cheaters.     

Cryptic differences in colour among Müllerian mimics: how can the visual capacities of predators and prey shape the evolution of wing colours?

Antagonistic interactions between predators and prey often lead to co‐evolution. In the case of toxic prey, aposematic colours act as warning signals for predators and play a protective role. Evolutionary convergence in colour patterns among toxic prey evolves due to positive density‐dependent selection and the benefits of mutual resemblance in spreading the mortality cost of educating predators over a larger prey assemblage. Comimetic species evolve highly similar colour patterns, but such convergence may interfere with intraspecific signalling and recognition in the prey community, especially for species involved in polymorphic mimicry. Using spectrophotometry measures, we investigated the variation in wing coloration among comimetic butterflies from distantly related lineages. We focused on seven morphs of the polymorphic species Heliconius numata and the seven corresponding comimetic species from the genus Melinaea. Significant differences in the yellow, orange and black patches of the wing were detected between genera. Perceptions of these cryptic differences by bird and butterfly observers were then estimated using models of animal vision based on physiological data. Our results showed that the most strikingly perceived differences were obtained for the contrast of yellow against a black background. The capacity to discriminate between comimetic genera based on this colour contrast was also evaluated to be higher for butterflies than for birds, suggesting that this variation in colour, likely undetectable to birds, might be used by butterflies for distinguishing mating partners without losing the benefits of mimicry. The evolution of wing colour in mimetic butterflies might thus be shaped by the opposite selective pressures exerted by predation and species recognition.     

Incorporating Motion into Investigations of mimicry

During the past thirty years, natural selection due to predation has been investigated with regard to prey motion in three areas that are relevant to the evolution of mimicry: (1) anti-apostatic selection, (2) locomotor mimicry, and (3) escape mimicry. Anti-apostatic selection, or selection against the odd individuals, arises when prey are at very high densities or when prey are Müllerian mimics. When prey are at high densities, motion of the prey increases selection against odd individuals. When the prey are Müllerian mimics, motion may also play an important role in strengthening selection against odd individuals. This may explain locomotor mimicry between Müllerian mimics. Locomotor mimicry arises when two distantly-related prey species appear alike in behaviour, and there is a corresponding suite of morphological, physiological, and biomechanical traits that the prey have in common. Locomotor mimicry has been demonstrated in Müllerian mimics. It is also predicted to occur in Batesian mimics but with important limitations due to selection by the predator for the prey to maintain the ability to escape if detected. Locomotor mimicry may also occur between palatable species that are alike as a result of unprofitable prey (or escape) mimicry. Escape mimicry arises when prey are difficult to capture. By frustration learning, the predator associates the colour of the prey with unprofitability. In all three instances, dis-similarity in colour or motion probably increases selection against the odd individual. In addition, the interaction of colour and motion gives rise to greater reliability of the signals to a specialist predator. However for a generalist predator, multiple component signals of the prey lead to errors in signal perception and greater risk of cheating. This revised version was published online in July 2006 with corrections to the Cover Date.     

Effects of group behavior in the predatory raid on damselfish nests by the false cleanerfish Aspidontus taeniatus

The false cleanerfish Aspidontus taeniatus, which resembles the bluestreak cleaner wrasse Labroides dimidiatus, is one of the best-known examples of mimicry in vertebrates. This mimicry system has been viewed as an aggressive mimicry to bite fish fins. However, recent field studies have reported that large individuals of the false cleanerfish often form groups and jointly raid damselfish nests to eat eggs that are guarded by their parents. The benefits of group behavior have been reported in a variety of animals. In the case of false cleanerfish, parental defense of territorial damselfishes is the main factor that constrains the availability of nutritionally valuable food resources. Here, we conducted field observations on the reefs of Okinawa, and found that the false cleanerfish formed groups of 2–12 individuals when they raided breeding nests of 13 species of damselfishes (Pomacentridae) and one species of triggerfish (Balistidae). Since the cleaner wrasse does not form such groups, the feeding groups of the false cleanerfish are assumed to reduce the effectiveness of mimicry. However, our results showed that the group behavior has two effects: a dilution effect, which reduces the risk of being attacked by egg-guarding fish, and an increase in foraging efficiency. We conclude that the false cleanerfish need to form foraging groups during egg-eating because the mimicry has no effect on parental damselfishes.     

Experimentally increased badge size increases male competition and reduces male parental care in the collared flycatcher

Experimental enlargement of sexually selected traits that are energetically cheap to produce is expected to reveal costs resulting from increased risk of predation or social competition. Given a trade-off between sexually selected traits and life history traits such costs may be expected to affect not only the males themselves but also their offspring. In this study I manipulated the size of the forehead patch, a sexually selected trait that functions as a badge of status in male collared flycatchersFicedula albicollis). First, I found that a male''s likelihood to establish a breeding territory with respect to his original badge size was affected by the treatment such that old males (older than or equal to two years) with relatively small original badges enjoyed an increased likelihood of establishing a breeding territory while young males (yearlings) suffered a reduced likelihood of establishment when their badges were enlarged as compared to unchanged. Second, young males with enlarged badges that were able to establish a territory fed their nestlings less in relation to their females compared to the control males. However, the females adjusted their parental effort to such an extent that no significant differences were observed in total feeding rate nor in reproductive success between the two groups of males. These results suggest that experimentally enlarged badge size in the collared flycatcher may result in increased male competition and that males have to trade their effort spent in male contest against their parental effort.