有无反馈对欺骗过程的神经机制的调控作用

欺骗行为会导致欺骗结果的产生,欺骗结果又会直接影响欺骗行为的发生及其内在机制.虽然有研究表明,欺骗结果会对相应的欺骗过程产生调控作用,但对这一调控作用的机制并不清楚.本研究采用功能核磁共振技术,对两组被试分别使用有、无反馈(欺骗结果)的GKT范式并记录两组被试在进行诚实反应和欺骗反应时的大脑激活模式.结果发现,有反馈组与无反馈组相比,有反馈组的诚实反应和欺骗反应都导致了左侧顶叶皮层、左背部前扣带皮层、左侧脑岛、双侧视皮层和右侧小脑的更大激活;对两组而言,欺骗反应和诚实反应都导致了右腹外侧前额区域、双侧缘上回、左侧脑岛、右后内侧额叶、右侧颞中回和右侧纹状体的更大激活;此外,与无反馈组相比,有反馈组的欺骗反应与诚实反应在双侧纹状体和左侧脑岛上的激活差异更加明显.这些结果表明,有无欺骗结果对欺骗过程的神经机制具有调控作用,当需要面临欺骗结果时,欺骗过程将更大程度地涉及到奖赏预期和风险厌恶过程的参与.     

Getting back to the rough ground: deception and 'social living'

At the heart of the social intelligence hypothesis is the central role of 'social living'. But living is messy and psychologists generally seek to avoid this mess in the interests of getting clean data and cleaner logical explanations. The study of deception as intelligent action is a good example of the dangers of such avoidance. We still do not have a full picture of the development of deceptive actions in human infants and toddlers or an explanation of why it emerges. This paper applies Byrne & Whiten's functional taxonomy of tactical deception to the social behaviour of human infants and toddlers using data from three previous studies. The data include a variety of acts, such as teasing, pretending, distracting and concealing, which are not typically considered in relation to human deception. This functional analysis shows the onset of non-verbal deceptive acts to be surprisingly early. Infants and toddlers seem to be able to communicate false information (about themselves, about shared meanings and about events) as early as true information. It is argued that the development of deception must be a fundamentally social and communicative process and that if we are to understand why deception emerges at all, the scientist needs to get 'back to the rough ground' as Wittgenstein called it and explore the messy social lives in which it develops.     

Orchid pollination by sexual deception: pollinator perspectives

The extraordinary taxonomic and morphological diversity of orchids is accompanied by a remarkable range of pollinators and pollination systems. Sexually deceptive orchids are adapted to attract specific male insects that are fooled into attempting to mate with orchid flowers and inadvertently acting as pollinators. This review summarises current knowledge, explores new hypotheses in the literature, and introduces some new approaches to understanding sexual deception from the perspective of the duped pollinator. Four main topics are addressed: (1) global patterns in sexual deception, (2) pollinator identities, mating systems and behaviours, (3) pollinator perception of orchid deceptive signals, and (4) the evolutionary implications of pollinator responses to orchid deception, including potential costs imposed on pollinators by orchids. A global list of known and putative sexually deceptive orchids and their pollinators is provided and methods for incorporating pollinator perspectives into sexual deception research are provided and reviewed. At present, almost all known sexually deceptive orchid taxa are from Australia or Europe. A few sexually deceptive species and genera are reported for New Zealand and South Africa. In Central and Southern America, Asia, and the Pacific many more species are likely to be identified in the future. Despite the great diversity of sexually deceptive orchid genera in Australia, pollination rates reported in the literature are similar between Australian and European species. The typical pollinator of a sexually deceptive orchid is a male insect of a species that is polygynous, monandrous, haplodiploid, and solitary rather than social. Insect behaviours involved in the pollination of sexually deceptive orchids include pre‐copulatory gripping of flowers, brief entrapment, mating, and very rarely, ejaculation. Pollinator behaviour varies within and among pollinator species. Deception involving orchid mimicry of insect scent signals is becoming well understood for some species, but visual and tactile signals such as colour, shape, and texture remain neglected. Experimental manipulations that test for function, multi‐signal interactions, and pollinator perception of these signals are required. Furthermore, other forms of deception such as exploitation of pollinator sensory biases or mating preferences merit more comprehensive investigation. Application of molecular techniques adapted from model plants and animals is likely to deliver new insights into orchid signalling, and pollinator perception and behaviour. There is little current evidence that sexual deception drives any species‐level selection on pollinators. Pollinators do learn to avoid deceptive orchids and their locations, but this is not necessarily a response specific to orchids. Even in systems where evidence suggests that orchids do interfere with pollinator mating opportunities, considerable further research is required to determine whether this is sufficient to impose selection on pollinators or generate antagonistic coevolution or an arms race between orchids and their pollinators. Botanists, taxonomists and chemical ecologists have made remarkable progress in the study of deceptive orchid pollination. Further complementary investigations from entomology and behavioural ecology perspectives should prove fascinating and engender a more complete understanding of the evolution and maintenance of such enigmatic plant‐animal interactions.     

Counterfactual Consent and the Use of Deception in Research

The use of deception for the purposes of research is a widespread practice within many areas of study. If we want to avoid either absolute acceptance or absolute rejection of this practice then we require some method of distinguishing between those uses of deception which are morally acceptable and those which are not. In this article I discuss the concept of counterfactual consent, and propose a related distinction between counterfactual‐defeating deception and counterfactual‐compatible deception. The aim is to show that this proposed distinction will be useful in furthering the debate regarding the use of deception for the purposes of research.     

Pollen transfer efficiency and its effect on inflorescence size in deceptive pollination strategies

Pollination systems differ in pollen transfer efficiency, a variable that may influence the evolution of flower number. Here we apply a comparative approach to examine the link between pollen transfer efficiency and the evolution of inflorescence size in food and sexually deceptive orchids. We examined pollination performance in nine food‐deceptive, and eight sexually deceptive orchids by recording pollen removal and deposition in the field. We calculated correlations between reproductive success and flower number (as a proxy for resources allocated during reproductive process), and directional selection differentials were estimated on flower number for four species. Results indicate that sexually deceptive species experience decreased pollen loss compared to food‐deceptive species. Despite producing fewer flowers, sexually deceptive species attained levels of overall pollination success (through male and female function) similar to food‐deceptive species. Furthermore, a positive correlation between flower number and pollination success was observed in food‐deceptive species, but this correlation was not detected in sexually deceptive species. Directional selection differentials for flower number were significantly higher in food compared to sexually deceptive species. We suggest that pollination systems with more efficient pollen transfer and no correlation between pollination success and number of flowers produced, such as sexual deception, may allow the production of inflorescences with fewer flowers that permit the plant to allocate fewer resources to floral displays and, at the same time, limit transpiration. This strategy can be particularly important for ecological success in Mediterranean water‐deprived habitats, and might explain the high frequency of sexually deceptive species in these specialised ecosystems.     

兰科植物欺骗性传粉

植物与传粉动物的互利关系在生态系统中非常普遍。然而,有许多植物不为传粉者提供任何报酬,而是利用各种欺骗方式诱骗昆虫拜访,从而实现传粉,即欺骗性传粉。兰科是被子植物大科之一,其高度特化的繁殖器官和适应于昆虫传粉的精巧结构令人称奇。进化论创始人达尔文描述了许多兰花与昆虫精巧的传粉系统,但他忽视了欺骗性传粉的存在。事实上,近1/3的兰科植物都依赖于欺骗性传粉。欺骗性传粉可能是导致兰科植物多样性的重要原因之一。兰花利用或操作昆虫觅食、交配、产卵和栖息等行为,演化出各种各样的欺骗性传粉机制,常见的类型包括泛化的食源性欺骗、Batesian拟态、性欺骗、产卵地拟态和栖息地拟态。花的颜色、形态和气味在欺骗性传粉的成功实现中起到了重要作用。欺骗性兰花与传粉昆虫之间的演化可能是不同步的,兰花追踪昆虫的行为信号而发生分化,然而欺骗性传粉可能对昆虫造成一定的伤害,从而对昆虫也施加选择压力。由于昆虫的学习行为,欺骗性的兰花一般具有低的昆虫拜访率和结实率,其繁殖成功率受各种因素的影响。欺骗性加剧了兰花对传粉昆虫的依赖,使其具有更高的灭绝风险,传粉生物学的研究能为兰科植物的有效保护提供指导。在欺骗性传粉系统中,有报酬的伴生植物、拟态模型和其他拟态信号提供者对传粉成功有重要影响。因此,研究欺骗性传粉兰花、传粉昆虫和相关的生物和生态因子的网状进化关系具有重要理论和实践意义。     

Understanding Mimicry – with Special Reference to Vocal Mimicry

The term mimicry was introduced to biology in 1862 by Henry Walter Bates in his evolutionary explanation of deceptive communication in nature, based on a three‐part interaction system of a mimicked organism or object (called model), a mimicking organism (called mimic), and one or more organisms as selecting agents. Bates gave two incongruous definitions of mimicry: one from the viewpoint of a natural agent that selects for, and in consequence is deceived by, the close resemblance of a toxic model's warning signal and the similar appearance of a palatable mimic, and another one from the viewpoint of a human taxonomist who under an evolutionary aspect focuses on convergent resemblance between model and mimic. Later definitions of Müllerian (F. Müller), arithmetic (A. Wallace) and social (M. Moynihan) mimicry abolish deception in the natural selecting agent, rely on the convergence criterion alone, fuse the roles of model and mimic but have to accept a mix of homologous and convergent resemblance amongst them for a functional explanation. The definition of vocal mimicry (E. Armstrong) refers to a learned resemblance between mimic and heterospecific model by character duplication (no convergence), so far without known (deceived or not deceived) natural selecting agents. It excludes Batesian vocal mimicry. The functional ethological understanding of mimicry as a tripartite communication system (W. Wickler) is consistent with Bates' concept and accepts deception as key element of Batesian mimicry beyond homologous and convergent resemblances. Deception is seen as caused by the divergence between a sign and its meaning for the natural selecting agent. This understanding covers mimicry in all behaviour domains, provides a generally applicable definition of mimic and model so far missing in any mimicry concept, and it distinguishes – still in line with Henry Bates – cultural from genetically determined model‐mimic‐resemblance; this applies to vocal mimicry in particular. Convergently evolved model‐mimic‐resemblance, not essential in Batesian mimicry but mandatory for its alternatives, marks a fundamental distinction between Batesian mimicry (including Mimesis) and all other conceptualized mimicries and accounts for the non‐existence of a unified meaning of the term mimicry. However, character convergence does not help to explain the mere existence of mimicry phenomena and is irrelevant for their permanence in nature. I therefore propose to remove the convergence argument from any mimicry definition.     

Behaviour of sexually deceived ichneumonid wasps and its implications for pollination in Cryptostylis (Orchidaceae)

Pollination via sexual deception is hypothesised to be associated with more frequent outcrossing and greater pollen dispersal distances than strategies involving food‐foraging behaviour. In this study, we investigated the behaviour and movement distances of Lissopimpla excelsa (Hymenoptera: Ichneumonidae), and their implications for the pollination of the sexually deceptive Cryptostylis ovata (Orchidaceae). Pollinator observations revealed that while L. excelsa will alight on multiple flowers within a single visit to a patch of orchids, the frequency of attempted copulation decreases with successive visits, suggesting that pollinator learning may inhibit within‐patch pollen transfer. Mark‐recapture demonstrated that 25% of wasps revisited inflorescences within a day and 50% revisited within a week. Despite the apparent site fidelity of some individuals, L. excelsa often move over large distances (maximum = 625 m), and are capable of dispersing pollen between patches. To resolve the consequences of pollination by sexual deception of ichneumonids, we compared our results with those from studies of other sexually deceptive systems. While pollination rates were comparable with other sexually deceptive orchids, L. excelsa showed high rates of column contact and moved over large distances relative to other sexually deceived pollinators. Among sexually deceptive orchids in general, the frequency of column contact was not correlated either with the frequency of pseudocopulation or with pollination rate. These results suggest that the consequences of pollination by sexual deception may vary extensively between plant taxa due to variation in floral traits, and behavioural differences between pollinator groups.     

Are open‐Label Placebos Ethical? Informed Consent and Ethical Equivocations

The doctor‐patient relationship is built on an implicit covenant of trust, yet it was not until the post‐World War Two era that respect for patient autonomy emerged as an article of mainstream medical ethics. Unlike their medical forebears, physicians today are expected to furnish patients with adequate information about diagnoses, prognoses and treatments. Against these dicta there has been ongoing debate over whether placebos pose a threat to patient autonomy. A key premise underlying medical ethics discussion is the notion that the placebo effect necessitates patient deception. Indeed, the American Medical Association guidelines imply that placebo treatment necessary entails a form of deception. As a consequence of this assumption, the fulcrum of debate on the use of placebo treatment has hinged on whether that deception is ever justified. Recently performed experiments with open‐label transparently prescribed placebos have begun to challenge the notion that deception is necessary in eliciting the placebo effect and such effects necessarily involve a binary distinction between autonomy and beneficence. In this article we focus on the content of disclosures in distinctive open‐label, transparently disclosed placebo studies and inquire whether they might be said to invoke deception in clinical contexts, and if so, whether the deception is unethical. We find that open placebos may be said to involve equivocation over how placebos work. However, drawing on surveys of patient attitudes we suggest that this equivocation appears to be acceptable to patients. We conclude that open placebos fulfil current American Medical Association guidelines for placebo use, and propose future research directions for harnessing the placebo effect ethically.     

Receivers limit the prevalence of deception in humans: evidence from diving behaviour in soccer players

Deception remains a hotly debated topic in evolutionary and behavioural research. Our understanding of what impedes or facilitates the use and detection of deceptive signals in humans is still largely limited to studies of verbal deception under laboratory conditions. Recent theoretical models of non-human behaviour have suggested that the potential outcome for deceivers and the ability of receivers to discriminate signals can effectively maintain their honesty. In this paper, we empirically test these predictions in a real-world case of human deception, simulation in soccer. In support of theoretical predictions in signalling theory, we show that cost-free deceit by soccer players decreases as the potential outcome for the signaller becomes more costly. We further show that the ability of receivers (referees) to detect deceptive signals may limit the prevalence of deception by soccer players. Our study provides empirical support to recent theoretical models in signalling theory, and identifies conditions that may facilitate human deception and hinder its detection.     

Pollen limitation and fruiting failure related to canopy closure in Calypso bulbosa (Orchidaceae), a northern food‐deceptive orchid with a single flower

Natural fruit set is constrained by pollen limitation and fruiting failure, and pollen limitation is expected to be especially severe in deceptive orchids. We performed hand cross‐pollinations in ten populations of a food‐deceptive orchid, Calypso bulbosa, under sparse and dense canopies in three non‐consecutive years. We explored the relationships between natural fruit set, pollen limitation and fruiting failure. Mean natural fruit set over the years was 60%, which is exceptionally high for a deceptive orchid. On average, hand cross‐pollination increased fruit set by 23%. Among open‐pollinated plants that did not set a fruit, 55.5% were estimated to be pollen limited and 44.5% to be limited by fruiting failure, i.e. inability to set a fruit after pollination. In species with high natural fruit set, hand cross‐pollination experiments may not always detect statistically significant pollen limitation. In our case, pollen limitation tended to become significant when the natural fruit set dropped below 60%. Canopy cover had a significant effect on fruiting failure, which was more severe under a dense canopy. Although our results demonstrate pollen limitation in many cases, they also highlight the fact that food deception can be a very effective pollination strategy. © 2013 The Linnean Society of London, Botanical Journal of the Linnean Society, 2013 , 171 , 744–750.     

Generalized food deception: colour signals and efficient pollen transfer in bee‐pollinated species of Eulophia (Orchidaceae)

Non‐rewarding plants use a variety of ruses to attract their pollinators. One of the least understood of these is generalized food deception, in which flowers exploit non‐specific food‐seeking responses in their pollinators. Available evidence suggests that colour signals, scent and phenology may all play key roles in this form of deception. Here we investigate the pollination systems of five Eulophia spp. (Orchidaceae) lacking floral rewards. These species are pollinated by bees, notably Xylocopa (Anthophorinae, Apidae) or Megachile (Megachilidae) for the large‐flowered species and anthophorid (Anthophorinae, Apidae) or halictid (Halictidae) bees for the small‐flowered species. Spectra of the lateral petals and ultraviolet‐absorbing patches on the labella are strongly contrasting in a bee visual system, which may falsely signal the presence of pollen to bees. All five species possess pollinarium‐bending mechanisms that are likely to limit pollinator‐mediated self‐pollination. Flowering times extend over 3–4 months and the onset of flowering was not associated with the emergence of pollinators, some of which fly year round. Despite sharing pollinators with other plants and lacking rewards that would encourage fidelity, the Eulophia spp. exhibited relatively high levels of pollen transfer efficiency compared with other rewarding and deceptive orchids. We conclude that the study species employ generalized food deception and exploit food‐seeking bees. © 2013 The Linnean Society of London, Botanical Journal of the Linnean Society, 2013 , 171 , 713–729.     

Patterns of deception in intersexual and intrasexual mating strategies

The act frequency approach (Buss 1988) was used to develop a taxonomy of deceptive mating acts and tactics and to investigate hypothesized sex differences in the use of these acts and tactics. The results indicate that males show differences in the types of deceptive acts and tactics used in intersexual versus intrasexual contexts. Intrasexually, males more frequently engage in deceptive acts and tactics related to the exaggeration of superiority and exaggeration of sexual promiscuity, intensity, and popularity. More frequent deceptive intersexual acts and tactics for males include feigned commitment, feigned sincerity, and feigned resource acquisition ability. Females more frequently engage in deceptive acts and tactics related to appearance alteration in both intersexual and intrasexual contexts. It was also found that males use deceptive intrasexual acts and tactics more frequently than females. These findings suggest that the dimensions of deception characteristic of male reproductive strategies are congruent with female mate selection criteria and the dimensions of deception characteristic of female reproductive strategies are congruent with male mate selection criteria. Results are interpreted in terms of current evolutionary psychological approaches to the understanding of sex differences in human mating strategies and the role of deception in intepersonal interaction.     

Positive effect of the yellow morph on female reproductive success in the flower colour polymorphic Iris lutescens (Iridaceae), a deceptive species

The deceptive Iris lutescens (Iridaceae) shows a heritable and striking flower colour polymorphism, with both yellow‐ and purple‐flowered individuals growing sympatrically. Deceptive species with flower colour polymorphism are mainly described in the family Orchidaceae and rarely found in other families. To explain the maintenance of flower colour polymorphism in I. lutescens, we investigated female reproductive success in natural populations of southern France, at both population and local scales (within populations). Female reproductive success was positively correlated with yellow morph frequency, at both the population scale and the local scale. Therefore, we failed to observe negative frequency‐dependent selection (NFDS), a mechanism commonly invoked to explain flower colour polymorphism in deceptive plant species. Flower size and local flower density could also affect female reproductive success in natural populations. Pollinator behaviour could explain the positive effect of the yellow morph, and our results suggest that flower colour polymorphism might not persist in I. lutescens, but alternative explanations not linked to pollinator behaviour are discussed. In particular, NFDS, although an appealingly simple explanation previously demonstrated in orchids, may not always contribute to maintaining flower colour polymorphism, even in deceptive species.     

Mechanisms and evolution of deceptive pollination in orchids

The orchid family is renowned for its enormous diversity of pollination mechanisms and unusually high occurrence of non-rewarding flowers compared to other plant families. The mechanisms of deception in orchids include generalized food deception, food-deceptive floral mimicry, brood-site imitation, shelter imitation, pseudoantagonism, rendezvous attraction and sexual deception. Generalized food deception is the most common mechanism (reported in 38 genera) followed by sexual deception (18 genera). Floral deception in orchids has been intensively studied since Darwin, but the evolution of non-rewarding flowers still presents a major puzzle for evolutionary biology. The two principal hypotheses as to how deception could increase fitness in plants are (i) reallocation of resources associated with reward production to flowering and seed production, and (ii) higher levels of cross-pollination due to pollinators visiting fewer flowers on non-rewarding plants, resulting in more outcrossed progeny and more efficient pollen export. Biologists have also tried to explain why deception is overrepresented in the orchid family. These explanations include: (i) efficient removal and deposition of pollinaria from orchid flowers in a single pollinator visit, thus obviating the need for rewards to entice multiple visits from pollinators; (ii) efficient transport of orchid pollen, thus requiring less reward-induced pollinator constancy; (iii) low-density populations in many orchids, thus limiting the learning of associations of floral phenotypes and rewards by pollinators; (iv) packaging of pollen in pollinaria with limited carry-over from flower to flower, thus increasing the risks of geitonogamous self-pollination when pollinators visit many flowers on rewarding plants. All of these general and orchid-specific hypotheses are difficult to reconcile with the well-established pattern for rewardlessness to result in low pollinator visitation rates and consequently low levels of fruit production. Arguments that deception evolves because rewards are costly are particularly problematic in that small amounts of nectar are unlikely to have a significant effect on the energy budget of orchids, and because reproduction in orchids is often severely pollen-, rather than resource-limited. Several recent experimental studies have shown that deception promotes cross-pollination, but it remains unknown whether actual outcrossing rates are generally higher in deceptive orchids. Our review of the literature shows that there is currently no evidence that deceptive orchids carry higher levels of genetic load (an indirect measure of outcrossing rate) than their rewarding counterparts. Cross-pollination does, however, result in dramatic increases in seed quality in almost all orchids and has the potential to increase pollen export (by reducing pollen discounting). We suggest that floral deception is particularly beneficial, because of its promotion of outcrossing, when pollinators are abundant, but that when pollinators are consistently rare, selection may favour a nectar reward or a shift to autopollination. Given that nectar-rewardlessness is likely to have been the ancestral condition in orchids and yet is evolutionarily labile, more attention will need to be given to explanations as to why deception constitutes an 'evolutionarily stable strategy'.     

Obvious pretence: for fun or for real? Cross-cousin and international relationships in Sri Lanka

Rather than understanding 'lying' or deception as a weapon of the oppressed, I use a Machiavellian and Nietzschean framework to investigate linguistic technologies of power that involve deception in contemporary Sri Lanka. My argument is based on distinct speech events collected in the village of Udahenagama and elite circles in Colombo: youthful flirtations, ritual negotiations with spirits, conversations with government officials and soldiers, a reported presidential diplomatic exchange, and everyday village banter. I highlight how the focus of the deceptive recorded interactions is revelation, rather than concealment, and I thereby propose a supplementary translation of the practice of telling boru , as obvious pretence. Obvious pretence is an important aspect of Sinhala linguistic technologies of power which imbue interdependent micro- and macro-level political spheres. I use Bakhtin's work on tones to describe how 'obvious pretence' intertwines, on the one hand, a tone of domination, aggression, and superiority, and, on the other hand, a tone of accommodation, conflict avoidance, and courtship. An aesthetic of power – as the power to deceive – lies in the tension between those two opposing tones, which are encompassed within the single linguistic and pragmatic practice of 'obvious pretence'.     

Chemical ecology and pollinator-driven speciation in sexually deceptive orchids

Sexually deceptive orchids mimic females of their pollinator species to attract male insects for pollination. Pollination by sexual deception has independently evolved in European, Australian, South African, and South American orchid taxa. Reproductive isolation is mainly based on pre-mating isolation barriers, the specific attraction of males of a single pollinator species, mostly bees, by mimicking the female species-specific sex-pheromone. However, in rare cases post-mating barriers have been found. Sexually deceptive orchids are ideal candidates for studies of sympatric speciation, because key adaptive traits such as the pollinator-attracting scent are associated with their reproductive success and with pre-mating isolation.During the last two decades several investigations studied processes of ecological speciation in sexually deceptive orchids of Europe and Australia. Using various methods like behavioural experiments, chemical, electrophysiological, and population-genetic analyses it was shown that minor changes in floral odour bouquets might be the driving force for pollinator shifts and speciation events. New pollinators act as an isolation barrier towards other sympatrically occurring species. Hybridization occurs because of similar odour bouquets of species and the overlap of flowering periods. Hybrid speciation can also lead to the displacement of species by the hybrid population, if its reproductive success is higher than that in the parental species.     

A specialised pollination system using nectar‐seeking thynnine wasps in Caladenia nobilis (Orchidaceae)

• Caladenia is a diverse Australian genus that is exceptional among orchids in having both species pollinated by food‐seeking and sexually deceived insects. Here, we investigated the pollination of Caladenia nobilis, a species predicted to be food‐deceptive due to its large, cream‐coloured and apparently nectarless flowers.
• Pollinator observations were made using experimental clumps of flowers. Measurements of floral colour were undertaken with a spectrometer, nectar was tested using GC‐MS, and reproductive success was quantified for 2 years.
• While C. nobilis attracted nine species of insect, only males of the thynnine wasp Rhagigaster discrepans exhibited the correct size and behaviour to remove and deposit pollen. Male R. discrepans attempted to feed from the surface of the labellum, often crawling to multiple flowers, but showed no evidence of sexual attraction. Most flowers produced little or no nectar, although some may provide enough sucrose to act as a meagre reward to pollinators. Floral colouration was similar to a related Caladenia species pollinated by sexual deception, although the sexually deceptive species had a dull‐red labellum. Reproductive success was generally low and highly variable between sites and years.
• In addition to most visitors being of inappropriate size for pollinia removal, the lack of response to the orchid by several co‐occurring species of thynnine wasp suggests filtering of potential pollinators at the attraction phase. Our discovery of a pollination strategy that may be intermediate between food deception and food reward raises the question, how many putatively rewardless orchids actually produce meagre amounts of nectar?

     

ECOLOGICAL AND GENETIC CONSEQUENCES OF POLLINATION BY SEXUAL DECEPTION IN THE ORCHID CALADENIA TENTACTULATA

Only orchids affect pollination by the deceptive sexual attraction of male insects, a syndrome particularly well developed in Australia. We examined the ecological and genetic consequences of exclusive pollination by sexually attracted male thynnine wasps in the orchid Caladenia tentaculata. Male wasps respond rapidly to flowers artificially presented in 1 × 1 m² experimental patches. Sixty of 287 wasps approached within centimeters of the flower, but did not land. Of the remaining 79% who made floral contact, only 7.5% attempted copulation, the step critical for pollination. Wasps only rarely moved among patches (19% of flights) and none attempted copulation a second time, resembling observations in natural populations. We confirmed outcrossing and long distance pollen flow by monitoring how colored pollen moved in natural populations. Pollen movements approximated a linear rather than a leptokurtic distribution (mean distance: 17 m; maximum: 58 m). Pollinator visits varied independently of flower density in three of four populations with most solitary flowers being visited. Allozyme analysis revealed within-population fixation indices (F) close to zero and low levels of differentiation (FST) among populations. Despite behavioral evidence for long distance pollen flow, significant local genetic structure exists, perhaps reflecting restricted seed dispersal. Long distance pollen flow in C. tentaculata may therefore promote outbreeding by minimizing pollen transfers among related neighbors. Although this species is self-compatible, outcrossed progeny develop significantly faster than selfed progeny. Effective pollination at low flower densities could accentuate this advantage. The data are consistent with the predictions that deceptive pollination will result in long distance pollen flow, which may be of selective advantage at low density. Comparative studies of how food reward, food deceptive, and sexual deceptive pollination systems vary within a phylogenetic framework could further illuminate the evolution of sexual deception.