Male response to an aggressive visual signal, the wing wave display, in swamp sparrows

Signaling often involves complex suites of behaviors that incorporate different sensory modalities. Whatever modality is used to establish that a signal functions in communication researchers must demonstrate that receivers respond to it. The territory defense response of male swamp sparrows involves a variety of behaviors that includes both vocal and visual displays. One of these, the “wing wave” display, is a distinctive movement that predicts physical attack. Here, we use robotic taxidermic mounts paired with song to test the hypothesis that wing waving is a signal and, specifically, that male receivers respond to wing waving as a signal of aggressive intent. As predicted, subjects responded more aggressively to the mount during wing waving trials than during stationary trials. A second experiment demonstrated that this effect cannot be attributed simply to increased attention to movement. Less expectedly, subjects did not alter their own display behavior in response to wing waving as compared to a static mount. We conclude that the wing wave display in the context of singing is a signal that functions in male–male aggressive communication. Questions remain, including whether wing waving functions as a signal in the absence of singing and whether wing waving and song are redundant signals or communicate different information.     

The honey bee shaking signal: function and design of a modulatory communication signal

This study explores the meaning and functional design of a modulatory communication signal, the honey bee shaking signal, by addressing five questions: (I) who shakes, (II) when do they shake, (III) where do they shake, (IV) how do receivers respond to shaking, and (V) what conditions trigger shaking. Several results confirm the work of Schneider (1987) and Schneider et al. (1986a): (I) most shakers were foragers (at least 83%); (II) shaking exhibited a consistent temporal pattern with bees producing the most signals in the morning (0810–1150 hours) just prior to a peak in waggle dancing activity; and (IV) bees moved faster (by 75%) after receiving a shaking signal. However, this study differs from previous work by providing a long-term, temporal, spatial, and vector analysis of individual shaker behavior. (III) Bees producing shaking signals walked and delivered signals in all areas of the hive, but produced the most shaking signals directly above the waggle dance floor. (IV) Bees responded to the signal by changing their direction of movement. Prior to receiving a signal, bees selected from the waggle dance floor moved, on average, towards the hive exit. After receiving a signal, some bees continued moving towards the exit but others moved directly away from the exit. During equivalent observation periods, non-shaken bees exhibited a strong tendency to move towards the hive exit. (V) Renewed foraging activity after food dearth triggered shaking signals, and, the level of shaking is positively correlated with the duration of food dearth. However, shaking signal levels also increased in the morning before foraging had begun and in the late afternoon after foraging had ceased. This spontaneous afternoon peak has not previously been reported. The shaking signal consequently appears to convey the general message “reallocate labor to different activities” with receiver context specifying a more precise meaning. In the context of foraging, the shaking signal appears to activate (and perhaps deactivate) colony foraging preparations. The generally weak response elicited by modulatory signals such as the shaking signal may result from a high receiver response threshold which allows the receiver to integrate multiple sources of information and which thereby increases the probability that receiver actions will be appropriate to colony needs. Received: 21 March 1997 / Accepted after revision: 30 August 1997     

Honey bee waggle dance communication: signal meaning and signal noise affect dance follower behaviour

Returning honey bee foragers perform waggle dances to inform nestmate foragers about the presence, location and odour of profitable food sources and new nest sites. The aim of this study is to investigate how the characteristics of waggle dances for natural food sources and environmental factors affect dance follower behaviour. Because food source profitability tends to decrease with increasing foraging distance, we hypothesised that the attractiveness of a dance, measured as the number of dance followers and their attendance, decreases with increasing distance to the advertised food location. Additionally, we determined whether time of year and dance signal noise, quantified as the variation in waggle run direction and duration, affect dance follower behaviour. Our results suggest that bees follow fewer waggle runs as the food source distance increases, but that they invest more time in following each dance. This is because waggle run duration increases with increasing foraging distance. Followers responded to increased angular noise in dances indicating more distant food sources by following more waggle runs per dance than when angular noise was low. The number of dance followers per dancing bee was also affected by the time of year and varied among colonies. Our results provide evidence that both noise in the message, that is variation in the direction component, and the message itself, that is the distance of the advertised food location, affect dance following. These results indicate that dance followers may pay attention to the costs and benefits associated with using dance information.     

Courtship display by great frigatebirds, Fregata minor: an energetically costly handicap signal?

We used detailed time-budget observations, mark-resight data, and doubly labeled water estimates of energy expenditure to test whether energy spent on courtship display by male frigatebirds functions as a sexually selected handicap signal. During a 2-day period of time budget observations, males displayed on average 29.5% of the time (range 0–100% for 15 different males), and this value was correlated with an index of season-long display effort. Season-long display effort was strongly predictive of pairing success. Average field metabolic rate (FMR) during the 2-day time budget period was 676.5 kJ/day (range 464.8–1035.0), substantially lower than the mass-specific FMR predicted from studies of other seabirds during incubation or chick-rearing. Despite a low overall FMR, display effort could function as an energetic handicap, either if FMR correlates positively with the amount of courtship performed or if high-quality males display at a high rate because they pay a lower energy cost per unit of display than do low-quality males. We found no relationship between FMR and display rate, despite good power for doing so. We also did not find a significant difference in energy spent divided by courtship time for males that were or were not chosen by females (inferred to be high- and low-quality males, respectively), though the medians differed in the predicted direction (preferred males having lower relative costs than non-preferred males) and the confidence interval on the difference between groups was very wide. Thus, we found evidence that male courtship effort is predictive of pairing success, we rejected one mechanism by which energetic cost of display could function as a handicap, and our test of the alternate energetic handicap mechanism was equivocal.     

Flexible bat echolocation: the influence of individual,habitat and conspecifics on sonar signal design

Acoustic signals which are used in animal communication must carry a variety of information and are therefore highly flexible. Echolocation has probably such functions and could prove as flexible. Measurable variabitlity can indicate flexibility in a behaviour. To quantify variability in bat sonar and relate to behavioural and environmental factors, I recorded echolocation calls of Euderma maculatum, Eptesicus fuscus, Lasiurus borealis and L. cinereus while the bats hunted in their natural habitat. I analysed 3390 search phase calls emitted by 16 known and 16 unknown individuals foraging in different environmental and behvioural situations. All four species used mainly multiharmonic signals that showed considerable intra- and inter-individual variability in the five signal variables I analysed (call duration, call interval, highest and lowest frequency and frequency with maximum energy) and also in the shape of the sonagram. A nested multivariate analysis of variance identified the influences of individual, hunting site, close conspecifics and of each observation on the frequency with maximum energy in the calls, and on other variables measured. Individual bats differed in multiple comparisons, most often in the main call frequency and least often in call interval. In a discriminant function analysis with resubstitution, 56–76% of a species' calls were assigned to the correct individual. Distinct individual call patterns were recorded in special situations in all species and the size of foraging areas in forested areas influenced temporal and spectral call structure. Echolocation behaviour was influenced by the presence of conspecifics. When bats were hunting together, call duration decreased and call interval increased in all species, but spectral effects were less pronounced. The role of morphometric differences as the source of individually distinct vocalizations is discussed. I also examined signal adaptations to long range echolocation and the influence of obstacle distance on echolocation call design. My results allow to discuss the problems of echo recognition and jamming avoidance in vespertilionid bats.     

Bird song as a signal of aggressive intent

A central question in animal communication research concerns the reliability of animal signals. The question is particularly relevant to aggressive communication, where there often may be advantages to signaling an exaggerated likelihood of attack. We tested whether aggressive signals are indeed reliable signals of attack in song sparrows (Melospiza melodia). We elicited aggressive signaling using a 1-min playback on a male’s territory, recorded the behavior of the male for 5 min, and then gave him the opportunity to attack a taxidermic mount of a song sparrow associated with further playback. Twenty subjects attacked the mount and 75 did not. Distance to the speaker was a significant predictor of attack for both the initial recording period and the 1 min before attack. For the initial recording period, none of the measures of singing behavior that we made was a significant predictor of attack, including song-type matching, type-switching frequency, and song rate. For the 1-min period immediately before attack, only the number of low amplitude “soft songs” was a significant predictor of attack. Although most aggressive signals contained little information on attack likelihood, as some models suggest should be the case, the unreliability of these signals was not caused by convergence of individuals on a single signaling strategy, as those models argue should occur.     

Size assessment via a visual signal in snapping shrimp

Snapping shrimp are highly aggressive decapod crustaceans, with large, asymmetric chelae. Body size determines the outcome of both inter- and intrasexual interactions. Both the body and chela sizes of mated pairs are correlated, but the body size correlation is significantly stronger. In competitive interactions between individuals of the same sex, larger individuals usually win. Because the size of the major chela is a function of body size in both males and females, chela size could be used to assess body size early in interactions, before engaging in more high risk behaviors. To determine whether the major chela is used in size assessment, I presented shrimp with isolated chelae. Male snapping shrimp responded aggressively to isolated chelae when they were fixed open in a display posture, and the degree of aggressive response depended on the relative size of the chela. These data provide direct experimental evidence for the use of a visual signal in size assessment. Females, in contrast, responded aggressively to both the open and closed chela, and their responses did not depend on relative size. This sex difference in response may be due to differences in the value of certain resources, such as shelters, to males and females: females may be more willing to respond aggressively regardless of the apparent size of their opponent, in order to acquire more reliable information regarding size, motivation or fighting ability. Received: 30 December 1994/Accepted after revision: 14 August 1995     

Vocal masculinity is a robust dominance signal in men

Dominance assessment is important in mating competition across a variety of species, but little is known about how individuals’ own quality affects their assessment of potential rivals. We conducted two studies to test whether men’s own dominance affects their attentiveness to a putative dominance signal, vocal masculinity, when assessing competitors. Study I examined dominance ratings made by men in relation to their self-rated physical dominance. Study II examined dominance ratings made by men in relation to objective measures of their physical dominance, including size, strength, testosterone, and physical aggressiveness. Vocal masculinity strongly affected dominance ratings, but a man’s own dominance did not alter his attention to vocal masculinity when assessing dominance. However, men who rated themselves high on physical dominance rated the voices of other men lower on dominance and reported more sex partners (study I). Men with intermediate testosterone concentrations rated the voices of other men lower on dominance (study II). These results confirm the effect of vocal masculinity on dominance perceptions, provide further evidence that dominance is relevant to mating success, and shed new light on how men assess the dominance of rivals and potential allies. Our results suggest that attention to dominance signals may depend less on the observer’s own dominance in species with coalitional aggression, where individuals must assess others not only in relation to themselves but also in relation to each other. Among men, the effect of a deep, masculine voice on perceptions of dominance appears to be robust and unmediated by the formidability of the listener.     

Alarm signal response in the brittle star Amphiura filiformis

 Flat fishes, such as the dab Limanda limanda, commonly prey on arms of Amphiura filiformis. We demonstrate in flume experiments that A. filiformis showed a more or less simultaneous response to an up-stream predation by dab on conspecifics: the arms, which are stretched up into the water column when filter feeding, responded by bending down to the sediment surface, and some arms submerged, at least partly, into the sediment. We interpret this as an alarm response. A similar, but significantly weaker response in A. filiformis was also recorded when dab ate Amphiura chiajei. Homogenates of the two Amphiura species and arm pinching – to simulate partial predation – elicited a similar response in A. filiformis, the arms bent to the sediment surface. In contrast, however, the behavioural response of the arms to the homogenates was to protrude further out of the sediment and sweep the surface vigorously. We interpret this as a feeding behaviour. Response to arm pinching was less clear. The ecological consequences and origin of alarm signal response in A. filiformis are discussed. Received: 8 February 1999 / Accepted: 16 July 1999     

The modulation of worker behavior by the vibration signal during house hunting in swarms of the honeybee, Apis mellifera

During house hunting, honeybee, Apis melli- fera, workers perform the vibration signal, which may function in a modulatory manner to influence several aspects of nestsite selection and colony movement. We examined the role of the vibration signal in the house-hunting process of seven honeybee swarms. The signal was performed by a small proportion of the older bees, and 20% of the vibrating bees also performed waggle dances for nestsites. Compared to non-vibrating controls, vibrating bees exhibited increased rates of locomotion, were more likely to move into the interiors of the swarms, and were more likely to fly from the clusters and perform waggle dances. Recipients responded to the signal with increased locomotion and were more likely than non- vibrated controls to fly from the swarms. Because vibration signals were intermixed with waggle dances by some vibrators, and because they stimulated flight in recipients, the signals may have enhanced nestsite scouting and recruitment early in the house-hunting process. All swarms exhibited increased vibration activity within 0.5–1 h of departure. During these final periods, numerous vibrating bees wove repeatedly in and out of the clusters while signaling and motion on the swarms increased until it culminated in mass flight. The peaks of vibration activity observed at the end of the house-hunting process may therefore have activated the entire swarm for liftoff once a new nestsite had been selected. Thus, the vibration signal may help to integrate the behavior of numerous groups of workers during nestsite selection and colony relocation. Received: 17 January 2000 / Received in revised form: 5 April 2000 / Accepted: 3 May 2000     

A global ecological signal of extinction risk in terrestrial vertebrates

To determine the distribution and causes of extinction threat across functional groups of terrestrial vertebrates, we assembled an ecological trait data set for 18,016 species of terrestrial vertebrates and utilized phylogenetic comparative methods to test which categories of habitat association, mode of locomotion, and feeding mode best predicted extinction risk. We also examined the individual categories of the International Union for Conservation of Nature Red List extinction drivers (e.g., agriculture and logging) threatening each species and determined the greatest threats for each of the four terrestrial vertebrate groups. We then quantified the sum of extinction drivers threatening each species to provide a multistressor perspective on threat. Cave dwelling amphibians (p < 0.01), arboreal quadrupedal mammals (all of which are primates) (p < 0.01), aerial and scavenging birds (p < 0.01), and pedal (i.e., walking) squamates (p < 0.01) were all disproportionately threatened with extinction in comparison with the other assessed ecological traits. Across all threatened vertebrate species in the study, the most common risk factors were agriculture, threatening 4491 species, followed by logging, threatening 3187 species, and then invasive species and disease, threatening 2053 species. Species at higher risk of extinction were simultaneously at risk from a greater number of threat types. If left unabated, the disproportionate loss of species with certain functional traits and increasing anthropogenic pressures are likely to disrupt ecosystem functions globally. A shift in focus from species- to trait-centric conservation practices will allow for protection of at-risk functional diversity from regional to global scales.     

The stop signal of honey bees: reconsidering its message

Summary The stop signal of honey bees has long been regarded as a vibrational begging signal produced by dance followers to elicit food from waggle dancers (Esch 1964). On the basis of playback experiments and behavioral analysis, this study presents the following evidence for a different signal function. Stop signals (1) can be produced by tremble dancers, dance followers, and waggle dancers; (2) rarely elicit trophallaxis; and (3) evidently cause waggle dancers to leave the dance floor. Subsequent work by Kirchner (submitted) using vibrational playback experiments confirms the latter observation. When the colony's food storers are temporarily overwhelmed by a large nectar influx, returning foragers will search for prolonged periods before unloading food and consequently begin to tremble dance (Seeley 1992). In this study, tremble dancers were the major producer of stop signals on the dance floor. The stop signal may thus retard recruitment until balance is restored.     

Stotting in Thomson's gazelles: an honest signal of condition

Summary The incidence and context of stotting were studied in Thomson's gazelles. Results suggested that gazelles were far more likely to stot in response to coursing predators, such as wild dogs, than they were to stalking predators, such as cheetahs. During hunts, gazelles that wild dogs selected stotted at lower rates than those they did not select. In addition, those which were chased, but which outran the predators, were more likely to stot, and stotted for longer durations, than those which were chased and killed. In response to wild dogs, gazelles in the dry season, which were probably in poor condition, were less likely to stot, and stotted at lower rates, than those in the wet season. We suggest that stotting could be an honest signal of a gazelle's ability to outrun predators, which coursers take into account when selecting prey.     

Complex signal function: developing a framework of testable hypotheses

The basic building blocks of communication are signals, assembled in various sequences and combinations, and used in virtually all inter- and intra-specific interactions. While signal evolution has long been a focus of study, there has been a recent resurgence of interest and research in the complexity of animal displays. Much past research on signal evolution has focused on sensory specialists, or on single signals in isolation, but many animal displays involve complex signaling, or the combination of more than one signal or related component, often serially and overlapping, frequently across multiple sensory modalities. Here, we build a framework of functional hypotheses of complex signal evolution based on content-driven (ultimate) and efficacy-driven (proximate) selection pressures (sensu Guilford and Dawkins 1991). We point out key predictions for various hypotheses and discuss different approaches to uncovering complex signal function. We also differentiate a category of hypotheses based on inter-signal interactions. Throughout our review, we hope to make three points: (1) a complex signal is a functional unit upon which selection can act, (2) both content and efficacy-driven selection pressures must be considered when studying the evolution of complex signaling, and (3) individual signals or components do not necessarily contribute to complex signal function independently, but may interact in a functional way.Communicated by A. Cockburn     

Trail discrimination signal of Lasius japonicus (Hymenoptera: Formicidae)

Summary. Trail-following behavior of Lasius japonicus was colony-specific in the field, while trail pheromone activity was not. We found that the footprint substance caused colony-specific trail-following behavior only when working in conjunction with the trail pheromone. The footprint substance alone did not lead the workers to follow trails. The substance consisted mainly of hydrocarbons with composition almost identical to that of cuticular hydrocarbons, except for the absence of n-alkanes. Nestmate workers shared footprint hydrocarbon profiles as well as cuticular hydrocarbons, but the profiles differed among colonies. We therefore consider that the footprint hydrocarbon profiles serve as the trail discrimination signal in L. japonicus.     

Melanin-based colorations signal strategies to cope with poor and rich environments

One hypothesis for the maintenance of genetic variation states that alternative genotypes are adapted to different environmental conditions (i.e., genotype-by-environment interaction G×E) that vary in space and time. Although G×E has been demonstrated for morphological traits, little evidence has been given whether these G×E are associated with traits used as signal in mate choice. In three wild bird species, we investigated whether the degree of melanin-based coloration, a heritable trait, covaries with nestling growth rate in rich and poor environments. Variation in the degree of reddish-brown phaeomelanism is pronounced in the barn owl (Tyto alba) and tawny owl (Strix aluco), and variation in black eumelanism in the barn owl and Alpine swift (Apus melba). Melanin-based coloration has been shown to be a criterion in mate choice in the barn owl. We cross-fostered hatchlings to test whether nestlings sired by parents displaying melanin-based colorations to different extent exhibit alternative growth trajectories when raised by foster parents in poor (experimentally enlarged broods) and rich (experimentally reduced broods) environments. With respect to phaeomelanism, barn owl and tawny owl offspring sired by redder parents grew more rapidly in body mass only in experimentally reduced broods. With respect to eumelanism, Alpine swift offspring of darker fathers grew their wings more rapidly only in experimentally enlarged broods, a difference that was not detected in reduced broods. These interactions between parental melanism and offspring growth rate indicate that individuals display substantial plasticity in response to the rearing environment which is associated with the degree of melanism: at least with respect to nestling growth, phaeomelanic and eumelanic individuals are best adapted to rich and poor environments, respectively. It now remains to be investigated why eumelanism and phaeomelanism have a different signaling function and what the lifelong consequences of these melanism-dependent allocation strategies are. This is important to fully appraise the role played by environmental heterogeneity in maintaining variation in the degree of melanin-based coloration.     

信号分子对类球红细菌(Rhodobacter sphaeroides)碳源利用的影响

类球红细菌拥有cer群体感应系统.它既有细胞间信息传递的功能,也对碳源利用进行调节.为调查自诱导物对碳源利用的影响,在仅少量EDTA作唯一能源物的培养基中加入N-(tetradecanoyl)-DL-homoserine lactone,通过测定活菌数变化观察这种类球红细菌自诱导物的结构类似物对碳源利用的影响.然后利用Biolog-GN鉴定板,在加入外源信号分子和对照的条件下,研究了类球红细菌正常培养与饥饿培养下对95种单一碳源的不同利用情况.结果表明,在存在信号分子的饥饿情况下,细菌能更好的利用EDTA维持活菌数量.当培养到6h的时候,加入信号分子培养的鉴定板中,正常培养情况下细菌对碳源的利用丰富度指数最高;而在饥饿培养情况下细菌能利用更多种类的碳源.     

A protein signal triggers sexual reproduction in Brachionus plicatilis (Rotifera)

The defining feature of the life cycle in monogonont rotifers such as Brachionus plicatilis (Muller) is alternation of asexual and sexual reproduction (mixis). Why sex is maintained in such life cycles is an important unsolved evolutionary question and one especially amenable to experimental analysis. Mixis is induced by a chemical signal produced by the rotifers which accumulates to threshold levels at high population densities. The chemical features of this signal were characterized using size exclusion, enzymatic degradation, protease protection assays, selective binding to anion ion exchange and C3 reversed phase HPLC columns, and the sequence of 17 N-terminal amino acids. These studies were carried out over two years beginning in 2003 using B. plicatilis Russian strain. When rotifer-conditioned medium was treated with proteinase K, its mixis-inducing ability was reduced by 70%. Proteinase K was added to medium auto-conditioned by 1 female ml⁻¹ where typically 17% of daughters became mictic and mixis was reduced to 1%. A cocktail of protease inhibitors added to conditioned medium significantly reduced degradation of the mixis signal by natural proteases. Conditioned medium subjected to ultrafiltration retained mixis-inducing activity in the >10 kDa fraction, but the <10 kDa fraction had no significant activity. The putative mixis signal bound to an anion exchange column, eluting off at 0.72 M NaCl. These fractions were further separated on a C3 reversed phase HPLC column and mixis-inducing activity was associated with a 39 kDa protein. Seventeen amino acids from the N-terminus have strong similarity to a steroidogenesis-inducing protein isolated from human ovarian follicular fluid. The 39 kDa protein is an excellent candidate for the rotifer mixis induction signal.