Oviposition by mutualistic seed-parasitic pollinators and its effects on annual fitness of single- and multi-flowered host plants

The balance of intimate relationships between plants and seed-eating pollinators can depend on pollinator behaviour in relation to floral characters, such as flower size and flower number. Here, we examined how pollinator oviposition in relation to these traits affected annual fitness (seed output) of single- and multi-flowered Trollius europaeus along altitudinal gradients in subarctic Sweden and the French Alps. Small flies (Chiastocheta spp.) pollinate T. europaeus and their larvae feed on developing seeds. Assuming that late flowers in multi-flowered plants attracted flies to the earliest flower on the same plant, we expected more eggs and higher seed predation in early multiple flowers than in single flowers. Relative seed predation would thereby increase with flower number. Both in Sweden and the Alps, more eggs were placed on large flowers. Early multiple flowers were slightly larger than single flowers, and about twice the size of secondary flowers. As a result, and possibly combined with the effects of secondary flowers, early multiple flowers attracted more ovipositing flies and experienced relatively higher seed predation. However, this did not generally result in higher seed predation of multi-flowered hosts. Multiple flowers had greater seed output than single flowers at all altitudes, also in the high alpine and subarctic sites, where single flowers were more abundant. We hypothesise that the distribution of multiple flowers generally is enforced by environmental factors, rather than by fly-host plant interactions, because only very rarely (in triple-flowered alpine plants) was seed predation disproportionate, and the relationship skewed to the disadvantage of the host. The outcome of the mutualistic interaction was often similar in alpine and subarctic populations, but the underlying factors were different. Subarctic flowers had high abortion and low predation rates, while alpine flowers experienced the reversed situation. The higher fly abundance in the Alps suggests a more intense mutualistic interaction than in Sweden. Despite varying ecological and environmental conditions at these sites, the mutualistic relationship was generally in balance. However, when it was unbalanced, this could be explained by fly behaviour in response to floral traits, and by differences in fly abundance. Received: 4 January 1999 / Accepted: 5 May 1999     

Variation in predation costs with Chiastocheta egg number on Trollius europaeus: how many seeds to pay for pollination?

1. In obligate plant/seed parasite–pollinator mutualisms, the plant is exclusively pollinated by an insect whose larvae are specific seed predators. Hence, outcomes of the interaction for the plant can vary with the number of eggs laid and the number of seeds eaten per larva. 2. In the work reported here, predation by Chiastocheta larvae on seeds of Trollius europaeus was analysed as a function of the number of eggs laid on the flower. Flowers with an increasing number of eggs were bagged in three populations and seeds were counted after the end of larval predation, in order to assess whether there was competition among larvae. 3. Seed predation on single‐egg flowers was high and variable (mean per population ranging from 15 to 40% of the developed seeds). Seed predation increased weakly with increasing egg load and was lower than gross seed production (always < 85%) whatever the number of eggs laid. This corresponds to a strong decrease in seed consumption per larva with increasing egg load, i.e. severe larval competition for resources. 4. The results suggest that both interference among Chiastocheta larvae and carpel dehiscence may protect T. europaeus seeds from total predation. Estimates of seed predation based on egg load observed in 20 natural populations in the French Alps typically ranged from 30 to 60%. The interaction was always beneficial for the plant and there was no risk of total seed destruction by Chiastocheta larvae, favouring stability of the mutualism.     

Distinguishing coevolution from covicariance in an obligate pollination mutualism: asynchronous divergence in Joshua tree and its pollinators

Obligate pollination mutualisms--in which both plants and their pollinators are reliant upon one another for reproduction--represent some of the most remarkable coevolutionary interactions in the natural world. The intimacy and specificity of these interactions have led to the prediction that the plants and their pollinators may be prone to cospeciation driven by coevolution. Several studies have identified patterns of phylogenetic congruence that are consistent with this prediction, but it is difficult to determine the evolutionary process that underlies these patterns. Phylogenetic congruence might also be produced by extrinsic factors, such as a shared biogeographic history. We examine the biogeographic history of a putative case of codivergence in the obligate pollination mutualism between Joshua trees (Yucca brevifolia) and two sister species of pollinating yucca moths (Tegeticula spp.) We employ molecular phylogenetic methods and coalescent-based approaches, in combination with relaxed-clock estimates of absolute rates of molecular evolution, to analyze multi-locus sequence data from more than 30 populations of Y. brevifolia and its pollinators. The results indicate that the moth species diverged significantly (p < 0.01) more recently than their corresponding host populations, suggesting that the apparent codivergence is not an artifact of a shared biogeographic history.     

The cost of mutualism: interactions between Trollius europaeus and its pollinating parasites

Summary Photosynthetic acclimation to 5 light environments ranging from 2 to 60% full sun was determined in Alocasia macrorrhiza, a shade tolerant species from tropical forest understories, and Colocasia esculenta, a cultivated species which occurs naturally in open marshy areas. Photosynthetic capacities of both species increased nearly 3 fold with increased photon flux density (PFD). In a given environment, however, photosynthetic capacities of C. esculenta were double those of A. macrorrhiza. Stomatal limitations explained only a small part of this difference. Respiration rates and estimated biochemical capacities increased in parallel to photosynthetic capacity. No differences were observed either between species or environments in the ratio of RuBP regeneration capacity to carboxylation capacity as determined from the CO₂ dependence response of photosynthesis. Quantum yields of both species decreased only slightly with increasing growth PFD, providing little evidence for photoinhibition at high PFD. The results are discussed in terms of the mechanisms of and limitations on acclimation in these two species.     

传粉细蛾与大戟科植物专性授粉的互惠共生体系

在已知的昆虫与植物所形成的专性授粉互惠共生体系中,榕树—榕小蜂、丝兰—丝兰蛾体系是经典实例,国内外学者已经从不同角度进行了大量的研究,为我们理解植物—传粉者互惠共生体系协同进化的机理和历史积累了宝贵的资料。近些年的研究发现鳞翅目细蛾科头细蛾属昆虫与大戟科植物之间也存在相似的协同进化关系。文章对国内外学者有关传粉细蛾与大戟科植物互惠共生协同进化的研究进行了整理。     

论昆虫与植物的相互作用和进化的关系

昆虫与植物是陆地生物群落中最为重要的组成部分,二者间的相互作用是多方面的,其中最为重要的是昆虫选择植物作为食物和生长场所、昆虫为植物传授花粉两方面。该文集中讨论这两方面的相互作用有哪些因素与进化有密切的关系。植食性昆虫根据其寄主植物范围,通常分为专食性（寄主范围窄）和广食性（寄主范围广）。从生态关系来看,广食性的取食行为比专食性的更为有利,但实际情况却与此相反,统观植食性昆虫的取食行为,有向专食性演化更为普遍的倾向。专食性发展有利于提高昆虫对寄主植物的选择效率,还可缓和天敌作用所造成的压力。根据昆虫与植物相互作用的特点,目前已提出很多昆虫与植物的进化理论,包括成对的协同进化、弥散的协同进化、群落的协同进化以及顺序进化。在昆虫对寄主植物的选择中,以植物对昆虫的影响较昆虫对植物的影响更为重要,称为顺序进化是适宜的;昆虫为被子植物传授花粉造成互惠共生,其中的进化关系应称为协同进化。     

Convergence and coevolution in a mutualism: evidence from a molecular phylogeny of Ficus

Abstract.— The interaction between Ficus (Moraceae) and their pollinating wasps (Chalcidoidea: Agaonidae; more than 700 species-specific couples) is one of the most specialized mutualisms found in nature. Both partners of this interaction show extensive variation in their respective biology. Here we investigate Ficus life-history trait evolution and fig/fig wasp coadaptation in the context of a well-resolved molecular phylogeny. Mapping out variations in Ficus life-history traits on an independently derived phylogeny constructed from ribosomal DNA sequences (external and internal transcribed spacer) reveals several parallel transitions in Ficus growth habit and breeding system. Convergent trait evolution might explain the discrepancies between morphological analyses and our molecular reconstruction of the genus. Morphological characters probably correlate with growth habit and breeding system and could therefore be subject to convergent evolution. Furthermore, we reconstruct the evolution of Ficus inflorescence characters that are considered adaptations to the pollinators. Our phylogeny reveals convergences in ostiole shape, stigma morphology, and stamen:ovule ratio. Statistical tests taking into account the phylogenetic relationship of the species show that transitions in ostiole shape are correlated with variation in wasp pollinator head shape, and evolutionary changes in stigma morphology and stamen:ovule ratio correlate with changes in the pollination behavior of the associated wasp. These correlations provide evidence for reciprocal adaptations of morphological characters between these mutualistic partners that have interacted over a long evolutionary time. In light of previous ecological studies on mutualism, we discuss the adaptive significance of these correlations and what they can tell us about the coevolutionary process occurring between figs and their pollinators.     

Lizards as a plant's 'hired help': letting pollinators in and seeds out

It is well-known that plants utilize many different kinds of animals for pollination and dispersal of their seeds, but an alternative kind of evolutionary relationship has attracted less attention: animals can facilitate pollen and seed transport without acting as a vector. We studied interactions between an epacridaceous plant (the honey bush, Richea scoparid) and a lizard (the snow skink, .Niveoscincus microtepidotus) near the summit of Mount Wellington, Tasmania. The lizards gain access to the plant's nectar by tearing the fused petals (the calyptra) from the flower, thus exposing the plant's reproductive organs. Snow skinks forage selectively on flowers with higher-than-average nectar content, suggesting that this behaviour has evolved in response to plant characteristics. Lizard foraging may benefit R. scoparia , because calyptra remain attached unless a lizard tears the flower open. Our experiments demonstrated that the lizard's calyptra removal dramatically increased the plant's seed release. In 60 fruits from flowers with their calyptra intact, no seeds at all were released. However, 57 out of 60 (87%) fruits from flowers with their calyptra removed by the lizards successfully released their seeds. This system appears to involve reciprocal evolutionary changes in the interacting species (behaviour in the lizards and reproductive morphology in the plant). Thus the system seems to provide an unusual case of coevolution.     

Cheating in mutualism: defection of Yucca baccata against its yucca moths

Yucca baccata cheats in its obligate pollination/seed predation mutualism with yucca moths. Although all individuals use the pollination services of yucca moths, many individuals do not reciprocate in sustaining yucca moth larvae. Cheating is associated with the morphology of Y. baccata pistils. In Y. baccata , the apex of the ovary contains only inviable ovules, and there are two distinct flower types, one of which has twice as many potentially viable ovules as the other. Because yucca moths oviposit at the apex of Y. baccata ovaries, larvae in flowers with few viable ovules fail to encounter viable ovules and therefore perish. Inflorescences generally have just one flower type, implying that some individuals cheat whereas others maintain the yucca moth population. Our most surprising observation, however, is that although the proportion of cheaters should be low, over 70% of Y. baccata individuals cheat. We hypothesize that both density- and frequency-dependent processes maintain a balance of cheaters and noncheaters in this system.     

Local adaptation and maladaptation to pollinators in a generalist geographic mosaic

The Geographic Mosaic Theory of Coevolution predicts the occurrence of mosaics of interaction-mediated local adaptations and maladaptations. Empirical support to this prediction has come mostly from specialist interactions. In contrast, local adaptation is considered highly unlikely in generalist interactions. In this study, we experimentally test local adaptation in a generalist plant-pollinator geographic mosaic, by means of a transplant experiment in which plants coming from two evolutionary hotspots and two coldspots were offered to pollinators at the same four localities. Plants produced in the hotspots attracted more pollinators in all populations, whereas coldspot plants attracted fewer pollinators in all populations. Differences in adaptation were not related to genetic similarity between populations, suggesting that it was mainly due to spatial variation in previous selective regimes. Our experiment provides the first strong support for a spatially structured pattern of adaptation and maladaptation generated by a generalist free-living mutualism.     

Geographical matching of volatile signals and pollinator olfactory responses in a cycad brood-site mutualism

Brood-site mutualisms represent extreme levels of reciprocal specialization between plants and insect pollinators, raising questions about whether these mutualisms are mediated by volatile signals and whether these signals and insect responses to them covary geographically in a manner expected from coevolution. Cycads are an ancient plant lineage in which almost all extant species are pollinated through brood-site mutualisms with insects. We investigated whether volatile emissions and insect olfactory responses are matched across the distribution range of the African cycad Encephalartos villosus. This cycad species is pollinated by the same beetle species across its distribution, but cone volatile emissions are dominated by alkenes in northern populations, and by monoterpenes and a pyrazine compound in southern populations. In reciprocal choice experiments, insects chose the scent of cones from the local region over that of cones from the other region. Antennae of beetles from northern populations responded mainly to alkenes, while those of beetles from southern populations responded mainly to pyrazine. In bioassay experiments, beetles were most strongly attracted to alkenes in northern populations and to the pyrazine compound in southern populations. Geographical matching of cone volatiles and pollinator olfactory preference is consistent with coevolution in this specialized mutualism.     

Making the most of your pollinators: An epiphytic fig tree encourages its pollinators to roam between figs

Ficus species are characterized by their unusual enclosed inflorescences (figs) and their relationship with obligate pollinator fig wasps (Agaonidae). Fig trees have a variety of growth forms, but true epiphytes are rare, and one example is Ficus deltoidea of Southeast Asia. Presumably as an adaptation to epiphytism, inflorescence design in this species is exceptional, with very few flowers in female (seed‐producing) figs and unusually large seeds. Figs on male (pollinator offspring‐generating) trees have many more flowers. Many fig wasps pollinate one fig each, but because of the low number of flowers per fig, efficient utilization by F. deltoidea''s pollinators depends on pollinators entering several female figs. We hypothesized that it is in the interest of the plants to allow pollinators to re‐emerge from figs on both male and female trees and that selection favors pollinator roaming because it increases their own reproductive success. Our manipulations of Blastophaga sp. pollinators in a Malaysian oil palm plantation confirmed that individual pollinators do routinely enter several figs of both sexes. Entering additional figs generated more seeds per pollinator on female trees and more pollinator offspring on male trees. Offspring sex ratios in subsequently entered figs were often less female‐biased than in the first figs they entered, which reduced their immediate value to male trees because only female offspring carry their pollen. Small numbers of large seeds in female figs of epiphytic F. deltoidea may reflect constraints on overall female fig size, because pollinator exploitation depends on mutual mimicry between male and female figs.     

Facultative mutualism between an herbivorous crab and a coralline alga: advantages of eating noxious seaweeds

Because encrusting coralline algae rely on herbivory or low light levels to prevent being overgrown by competitively superior fleshy algae, corallines are relatively rare in shallow areas with low rates of herbivory. In contrast to this general trend, the branching coralline alga Neogoniolithon strictum occurs primarily in shallow seagrass beds and along the margins of shallow reef flats where herbivory on macrophytes is low. This alga apparently persists in these habitats by providing refuge to the herbivorous crab Mithrax sculptus at mean densities of 1 crab per 75 g of algal wet mass. When crabs were removed from some host corallines, hosts without crabs supported 9 times the epiphytic growth of hosts with crabs after only 30 days. Crabs without access to a coralline alga were rapidly consumed by reef fishes, while most of those tethered near a host alga survived. These results suggest that the crabs clean their algal host of fouling seaweeds and associate with the host to minimize predation. However, to effectively clean the host, the crab must consume the wide array of macroalgae that commonly co-occur with coralline algae in these habitats, including chemically defended species in the genera Halimeda, Dictyota, and Laurencia. Crabs did readily consume these seaweeds, which were avoided by, and are chemically defended from, herbivorous fishes. Even though crabs readily consumed both Halimeda and Dictyota in whole-plant feeding assays, chemical extracts from these species significantly reduced crab feeding, suggesting that factors other than secondary chemistry (e.g., food value, protein, energy content), may determine whole-plant palatability. Having the ability to use a wide variety of foods, and choosing the most profitable rather than the least defended foods, would diminish foraging time, increase site fidelity, and allow the crab to function mutualistically with the host alga. Despite the obvious benefit of associating with N. strictum, M. sculptus did not prefer it over other habitats offering a structurally similar refuge, suggesting that these crabs are not N. strictum specialists, but rather occupy multiple habitats that provide protection from predators. Structurally complex organisms like N. strictum may commonly suppress competitors by harboring protective symbionts like M. sculptus. It is possible that diffuse coevolution has occurred between these two groups; however, this seems unlikely because both herbivore and host appear to respond most strongly to selective pressures from predators and competitors outside this association.     

Pollination and seed predation by moths on Silene and allied Caryophyllaceae: evaluating a model system to study the evolution of mutualisms

Nursery pollinators, and the plants they use as hosts for offspring development, function as exemplary models of coevolutionary mutualism. The two pre-eminent examples--fig wasps and yucca moths--show little variation in the interaction: the primary pollinator is an obligate mutualist. By contrast, nursery pollination of certain Caryophyllaceae, including Silene spp., by two nocturnal moth genera, Hadena and Perizoma, ranges from antagonistic to potentially mutualistic, offering an opportunity to test hypotheses about the factors that promote or discourage the evolution of mutualism. Here, we review nursery pollination and host-plant interactions in over 30 caryophyllaceous plants, based on published studies and a survey of researchers investigating pollination, seed predation, and moth morphology and behavior. We detected little direct evidence of mutualism in these moth-plant interactions, but found traits and patterns in both that are nonetheless consistent with the evolution of mutualism and merit further attention.     

The evolution of egg rejection by cuckoo hosts in Australia and Europe

Exploitation of hosts by brood parasitic cuckoos is expectedto stimulate a coevolutionary arms race of adaptations and counteradaptations.However, some hosts have not evolved defenses against parasitism.One hypothesis to explain a lack of host defenses is that thelife-history strategies of some hosts reduce the cost of parasitismto the extent that accepting parasitic eggs in the nest is evolutionarilystable. Under this hypothesis, it pays hosts to accept cuckooeggs if (1) the energetic cost of raising the cuckoo is low,(2) there is time to renest, and (3) clutch size is small. Weparasitized the nests of host and nonhost species with nonmimeticmodel eggs to test whether the evolution of egg recognitionby cuckoo hosts could be explained by life-history variablesof the host. The most significant factor explaining rates ofrejection of model eggs was whether or not a species was a cuckoohost, with hosts rejecting model eggs at a higher rate thannonhosts. Egg-rejection rates were also explained by visibilitywithin the nest and by cuckoo mass. We found little supportfor the life-history model of egg rejection. Our results suggestthat parasitism is always sufficiently costly to select forhost defenses and that the evolution of defenses may be limitedby proximate constraints such as visibility within the nest.     

Social learning of a brood parasite by its host

Arms races between brood parasites and their hosts provide model systems for studying the evolutionary repercussions of species interactions. However, how naive hosts identify brood parasites as enemies remains poorly understood, despite its ecological and evolutionary significance. Here, we investigate whether young, cuckoo-naive superb fairy-wrens, Malurus cyaneus, can learn to recognize cuckoos as a threat through social transmission of information. Naive individuals were initially unresponsive to a cuckoo specimen, but after observing conspecifics mob a cuckoo, they made more whining and mobbing alarm calls, and spent more time physically mobbing the cuckoo. This is the first direct evidence that naive hosts can learn to identify brood parasites as enemies via social learning.     

Associations between mycophagous Drosophila and their Howardula nematode parasites: a worldwide phylogenetic shuffle

Little is known about what determines patterns of host association of horizontally transmitted parasites over evolutionary timescales. We examine the evolution of associations between mushroom-feeding Drosophila flies (Diptera: Drosophilidae), particularly in the quinaria and testacea species groups, and their horizontally transmitted Howardula nematode parasites (Tylenchida: Allantonematidae). Howardula species were identified by molecular characterization of nematodes collected from wild-caught flies. In addition, DNA sequence data is used to infer the phylogenetic relationships of both host Drosophila (mtDNA: COI, II, III) and their Howardula parasites (rDNA: 18S, ITS1; mtDNA: COI). Host and parasite phylogenies are not congruent, with patterns of host association resulting from frequent and sometimes rapid host colonizations. Drosophila-parasitic Howardula are not monophyletic, and host switches have occurred between Drosophila and distantly related mycophagous sphaerocerid flies. There is evidence for some phylogenetic association between parasites and hosts, with some nematode clades associated with certain host lineages. Overall, these host associations are highly dynamic, and appear to be driven by a combination of repeated opportunities for host colonization due to shared breeding sites and large potential host ranges of the nematodes.     

Is there a floral parasite mutualism in cycad pollination? the pollination biology of Encephalartos villosus (Zamiaceae)

Observations and experiments were carried out over 5 yr to distinguish between wind and insect pollination in the cycad Encephalartos villosus Lemaire (Zamiaceae). They were also designed to determine whether a pollination mutualism exists between E. villosus and Antliarhinus zamiae (Thunberg) (Coleoptera: Brentidae), an obligate ovule parasite that routinely parasitizes a large proportion of the ovules. The percentage of fertilized ovules dropped slightly when wind was excluded from the megastrobilus. However, when insects were excluded by either net bags or insecticide there was a substantial decrease in the proportion of fertilized ovules. Five beetle species belonging to four families were found on the strobili at the time of pollination. Using data on the effectiveness of pollen transfer to the receptive ovule, as well as data on abundance and pollen loads, a pollinator importance value (PIV) was determined for each beetle species and a pollinator importance index (PII) was determined for each population. PII values showed that an undescribed weevil (Porthetes sp., Curculionidae) was consistently the most important pollinator. A. zamiae and an undescribed beetle species within the Xenoscelinae (Languriidae) played a minor role in pollination, and their contributions varied from year to year and between populations. Two additional beetle species, Metacucujus goodei Endrödy-Younga (Boganiidae) and a second species of Xenoscelinae, had very low PII values and probably had little or no effect on pollination. Low PIV scores for A. zamiae were a result of its low numbers on the microstrobilus and the tendency of the beetles to remain on the outside of the megastrobilus. In the interaction between E. villosus and A. zamiae, the cycad does not appear to benefit significantly from a pollination service and I interpret this to mean that the relationship is antagonistic rather than mutualistic. There is, however, a possible mutualism between Porthetes sp. and E. villosus.     

The evolution of nocturnal behaviour in sweat bees,Megalopta genalis and M. ecuadoria (Hymenoptera: Halictidae): an escape from competitors and enemies?

Evolutionary transitions to dim-light foraging (predawn matinal, crepuscular, nocturnal) have occurred repeatedly in bees, and may be associated with an escape from enemies or competitors. To date, however, little information has been available to test these hypotheses. Here we provide the first detailed information on the nesting behaviour of two species of Neotropical, nocturnal sweat bees, Megalopta genalis and M. ecuadoria (Hymenoptera: Halictidae). Females are facultatively social or solitary, and construct nests in dead wood. Nocturnal foraging behaviour is bimodal. Bees began foraging after sunset (∼18:30 h) and ceased foraging approximately 1 h later even though nocturnal flowers with pollen were still abundant; a second foraging bout occurred in the predawn morning, which began at ∼04:45 h and ended around sunrise (∼06:15 h) when diurnal-blooming flowers were abundant. Bees are capable of controlled flight in full light. They utilized pollen from both canopy and understory plant species, which have diurnal or nocturnal pollen anthesis. Megalopta nests are attacked by generalist predators such as ants, as well as the endoparasitic fly Melaloncha sp. nov. (Phoridae), the beetle Macrosaigon gracilis (Rhipophoridae), the parasitic wasp Lophostigma cincta (Mutillidae), and the brood parasite Megalopta byroni (Halictidae). Overall nest survivorship rates were comparable to those for diurnal relatives, but rates of cell parasitism for Megalopta (< < 5%) were substantially lower than they are for day-flying relatives, offering some support for the hypothesis that the evolution of nocturnal behaviour enables escape from natural enemies.  © 2004 The Linnean Society of London, Biological Journal of the Linnean Society , 2004, 83 , 377–387.