Ant behaviour and seed morphology: a missing link of myrmecochory

Seed dispersal by ants (myrmecochory) is mediated by the presence of a lipid-rich appendage (elaiosome) on the seed that induces a variety of ants to collect the diaspores. When seeds mature or fall onto the ground, these ant species transport them to their nest. After eating the elaiosome, the seed is discarded in nest galleries or outside, in the midden or farther away, where seeds can potentially germinate. The final location of seeds with their elaiosomes removed was evaluated to assess the importance of possible handles (structures that ants can grasp to carry) in transporting ants during re-dispersal experiments of seeds from nests of six species of ants. The results indicate that seeds remained within the nest because the ants were not able to transport them out of the nest. As a consequence of the elaiosome being removed, small ant species could not take Euphorbia characias seeds out of their nests. Only large ant species could remove E. characias seeds from their nests. Attaching an artificial handle to E. characias seeds allowed small ant species to redistribute the seeds from their nests. On the other hand, Rhamnus alaternus seeds that have a natural handle after the elaiosome removal were removed from the nests by both groups of ant species. If a seed has an element that acts as a handle, it will eventually get taken out of the nest. The ants’ size and their mandible gap can determine the outcome of the interaction (i.e. the pattern of the final seed shadow) and as a consequence, could influence the events that take place after the dispersal process.     

Indirect effects of granivory by harvester ants: plant species composition and reproductive increase near ant nests

Summary Of 36 plant species surveyed, 6 were significantly associated with nests of the desert seed-harvester ant Veromessor pergandei or Pogonomyrmex rugosus; two other plant species were significantly absent from ant nests. Seeds of two common desert annuals, Schismus arabicus and Plantago insularis, realize a 15.6 and 6.5 fold increase (respectively) in number of fruits or seeds produced per plant growing in ant nest refuse piles compared to nearby controls. Mass of individual S. arabicus seed produced by plants growing in refuse piles also increased significantly. Schismus arabicus, P. insularis and other plants associated with ant nests do not have seeds with obvious appendages attractive to ants. Dispersal and reproductive increase of such seeds may represent a relatively primitive form of ant-plant dispersal devoid of seed morphological specializations. Alternatively, evolution of specialized seed structures for dispersal may be precluded by the assemblage of North American seed-harvester ants whose workers are significantly larger than those ants normally associated with elaiosome-attached seed dispersal. Large worker size may permit consumption of elaiosome and seed.     

Population dynamics of the shrub Acacia suaveolens (Sm.) Willd.: Dispersal and the dynamics of the soil seed-bank

Genet survival in seeds of Acacia suaveolens was examined through both dispersal and dormancy in the soil in populations near Sydney. Following initial passive seed-fall, the majority of seeds lie within a 1 m radius of the stem of the parent. Further dispersal is predominately mediated by ants. A. suaveolens seeds possess an elaiosome which attracts ants. When elaiosomes are removed, the potential for further dispersal of seeds is greatly reduced. Three species of ant disperse seeds of A. suaveolens and the fate of seeds following ant dispersal was observed to depend on the particular species of ant involved. Ants of both Iridomyrmex sp. and Pheidole sp. B are too small to drag seeds and, instead, ants of these species usually remove the elaiosome in situ, with little dispersal of the-seed resulting. Ants of Pheidole sp. A are larger and disperse seeds further, frequently taking them into their nests where the elaisosome is removed. Seeds are retained inside the nests and incorporated into the floors and walls of passageways and chambers. Several supposed ‘advantages’ of myrmecochory were examined but none were verified. Instead, two distinct ‘disadvantages’ were identified. These were: burial of seeds by ants of Pheidole sp. A into ‘unsafe sites’; and too deep a burial of seeds in nests for seeds to receive a stimulus to germinate during fires, and for seedlings to emerge successfully. Outside nests of Pheidole sp. A. seeds are concentrated in the top 5 cm of the soil, whilst within nests of these ants, seeds are found up to 15 cm deep. The dynamics of various components of the soil seed-bank were examined using seeds buried in nylon mesh containers. The seed-bank is persistent without annual recruitment to seedlings, enabling a population to persist as seeds after all above-ground plants have perished.     

New mutualism for old: indirect disruption and direct facilitation of seed dispersal following Argentine ant invasion

The indirect effects of biological invasions on native communities are poorly understood. Disruption of native ant communities following invasion by the Argentine ant (Linepithema humile) is widely reported to lead indirectly to the near complete collapse of seed dispersal services. In coastal scrub in southeastern Australia, we examined seed dispersal and handling of two native and two invasive alien plant species at Argentine ant-invaded or -uninvaded sites. The Argentine ant virtually eliminates the native keystone disperser Rhytidoponera victoriae, but seed dispersal did not collapse following invasion. Indeed, Argentine ants directly accounted for 92% of all ant-seed interactions and sustained overall seed dispersal rates. Nevertheless, dispersal quantity and quality among seed species differed between Argentine ant-invaded and -uninvaded sites. Argentine ants removed significantly fewer native Acacia retinodes seeds, but significantly more small seeds of invasive Polygala myrtifolia than did native ants at uninvaded sites. They also handled significantly more large seeds of A. sophorae, but rarely moved them >5 cm, instead recruiting en masse, consuming elaiosomes piecemeal and burying seeds in situ. In contrast, Argentine ants transported and interred P. myrtifolia seeds in their shallow nests. Experiments with artificial diaspores that varied in diaspore and elaiosome masses, but kept seed morphology and elaiosome quality constant, showed that removal by L. humile depended on the interaction of seed size and percentage elaiosome reward. Small diaspores were frequently taken, independent of high or low elaiosome reward, but large artificial diaspores with high reward instead elicited mass recruitment by Argentine ants and were rarely moved. Thus, Argentine ants appear to favour some diaspore types and reject others based largely on diaspore size and percentage reward. Such variability in response indirectly reduces native seed dispersal and can directly facilitate the spread of an invasive alien shrub.     

Removal of seeds from Neotropical frugivore droppings

In a Costa Rican rain forest, the majority of tree and shrub species have their seeds dispersed by vertebrates. Over a third of the species' seeds are of a size accessible to, and primarily carried away by, ants. Frugivorous bird droppings come in sizes from a few seeds to over a thousand, with number of seeds isometric with bird body mass. Dropping size decreases as seeds are scattered by rain. Larger droppings produced from fruits ofMiconia affinis (Melastomataceae) are discovered and recruited to more by ants, with a diverse guild of 22 ant species carrying away the seeds. Droppings with 64 and 16 seeds were used by a subset of the ant community exploiting 4-seed droppings, likely due to resource defense by aggressive species. Seeds in the smallest droppings stood the smallest chance of being removed. Although soil-nesting ants of the tribe Attini were the primary removers of seeds in this forest, a third of removal was by ants living in ephemeral litter nests. Seeds ofM. affinis were found in litter ant nests in 8 of 28 1-m² plots, suggesting that seed rain was not highly localized. Since litter nests are common, contain few seeds/nest and are often abandoned by their ants, litter ants may be the best candidates for ant-plant dispersal mutualisms.     

Seed handling behaviours of native and invasive seed‐dispersing ants differentially influence seedling emergence in an introduced plant

相似文献   

Secondary seed dispersal by ants in Neotropical cerrado savanna: species‐specific effects on seeds and seedlings of Siparuna guianensis (Siparunaceae)

1. Most woody plant species in tropical habitats are primarily vertebrate‐dispersed, but interactions between ants and fallen seeds and fruits are frequent. This study assesses the species‐specific services provided by ants to fallen arillate seeds of Siparuna guianensis, a primarily bird‐dispersed tree in cerrado savanna. The questions of which species interact with fallen seeds, their relative contribution (versus vertebrates) to seed removal, and the potential effects on seedling establishment are investigated. 2. Seeds are removed in similar quantities in caged and control treatments, suggesting that ants are the main dispersers on the ground. Five ant species attended seeds. Pheidole megacephala (≈0.4 cm) cooperatively transported seeds, whereas the smaller Pheidole sp. removed the seed aril on spot. Large (> 1.0 cm) Odontomachus chelifer, Pachycondyla striata, and Ectatomma edentatum individually carried seeds up to 4 m. Bits of aril are fed to larvae and intact seeds are discarded near the nest entrance. 3. Overall, greater numbers of seedlings were recorded near ant nests than in control plots without nests. This effect, however, was only detected near P. megacephala and P. striata nests, where soil penetrability was greater compared with controls. Soil nutrients did not differ between paired plots. 4. This study confirms the prevalence of ant–seed interactions in cerrado and shows that ant‐derived benefits are species‐specific. Ant services range from seed cleaning on the spot to seed displacement promoting non‐random spatial seedling recruitment. Although seed dispersal distances by ants are likely to be shorter than those by birds, our study of S. guianensis shows that fine‐scale ant‐induced seed movements may ultimately enhance plant regeneration in cerrado.     

ANT DISPERSAL OF CALATHEA (MARANTACEAE) SEEDS BY CARNIVOROUS PONERINES (FORMICIDAE) IN A TROPICAL RAIN FOREST

Two tropical herbaceous plant species, Calathea microcephala and Calathea ovandensis, exhibit morphological adaptations for seed dispersal by ants. In the field, 21 ant species are attracted to the arils of the seeds. Previously known as predatory carnivores, the ponerine ants Odontomachus laticeps, O. minutus, Pachycondyla harpax, and P. apicalis carry the seeds toward their nests, behaving as though they were carrying prey. These ants remove the aril in the nest, and seeds without arils germinate more readily than seeds with arils. Ant foraging distances can account for seedling distributions. Myrmecochory may be far more common in tropical rain forests than has been previously suspected.     

Odor of achlorophyllous plants’ seeds drives seed‐dispersing ants

Seed dispersal by ants is an important means of migration for plants. Many myrmecochorous plants have specialized appendages in their seeds called elaiosome, which provides nutritional rewards for ants, and enable effective seed dispersal. However, some nonmyrmecochorous seeds without elaiosomes are also dispersed by ant species, suggesting the additional mechanisms other than elaiosomes for seed dispersal by ants. The seeds of the achlorophyllous and myco‐heterotrophic herbaceous plant Monotropastrum humile are very small without elaiosomes; we investigated whether odor of the seeds could mediate seed dispersal by ants. We performed a bioassay using seeds of M. humile and the ant Nylanderia flavipes to demonstrate ant‐mediated seed dispersal. We also analyzed the volatile odors emitted from M. humile seeds and conducted bioassays using dummy seeds coated with seed volatiles. Although elaiosomes were absent from the M. humile seeds, the ants carried the seeds to their nests. They also carried the dummy seeds coated with the seed volatile mixture to the nest and left some dummy seeds inside the nest and discarded the rest of the dummy seeds outside the nest with a bias toward specific locations, which might be conducive to germination. We concluded that, in M. humile seeds, volatile odor mixtures were sufficient to induce seed‐carrying behavior by the ants even without elaiosomes.     

Differential dispersal of Chamaesyce maculata seeds by two ant species in Japan

Seed dispersal by ants (myrmecochory) is a widely distributed plant–animal interaction in many ecosystems, and it has been regarded as a generalized (multiple species) interaction in which specialization on specific ant partners is uncommon. In this paper, we demonstrate species-specific seed dispersal of spotted spurge (Chamaesyce maculata) by ants in Japan. C. maculata produces seeds from summer to autumn in Japan. The seeds produced in autumn are carried by two ant species, Tetramorium tsushimae and Pheidole noda. We performed laboratory experiments to investigate the fate of C. maculata seeds in the nests of T. tsushimae and P. noda. P. noda consumed the seeds in the nest and rarely carried seeds out of the nest, while T. tsushimae consumed only the seed coat, and subsequently carried the seeds out of the nest. Removal of the seed coat by T. tsushimae may increase seed survival by reducing their susceptibility to infection by fungi. We also observed ant responses to filter paper soaked with an aqueous extract of the seed coat. P. noda did not react to the filter paper, but T. tsushimae carried the filter paper into their nest. Analysis by high-pressure liquid chromatography revealed that the aqueous extract contained at least four sugars and one unknown substance. Myrmecochory has been regarded as a generalized interaction with specialization for specific ant partners uncommon. However, our study suggests there is a species-specific interaction in seed dispersal by ants in autumn-flowering individuals of C. maculata in Japan.     

DISPERSAL ECOLOGY OF CAREX PEDUNCULATA (CYPERACEAE), A NEW NORTH AMERICAN MYRMECOCHORE

Carex pedunculata is the first North American species of the Cyperaceae that is identified as a myrmecochore. Many morphological and phenological features of this species and its breeding system are interpreted as adaptive for seed dispersal by ants. In laboratory tests, workers of the ant species Aphaenogaster rudis carry the diaspores to the nest, eat the elaiosomes, carry larvae to the elaiosomes to feed, and deposit diaspores whose elaiosomes have been eaten with other nest debris. The achenes then germinate. Achenes will also germinate without any handling by ants. Workers will also transport diaspores with uneaten elaiosomes when the nest is disturbed. Greenhouse tests show that seedling growth is greatly inhibited if a diaspore remains near the parent plant and cohort seedlings. Field studies of natural populations identify rotting logs (the location of ant nests) as forest floor microsites for colonization of C. pedunculata and other myrmecochores. Ant nesting behavior may pattern much of the herb stratum. This species is self-compatible, and single seeds may start successful new populations. Three processes contribute to population growth: vegetative growth, germination of untransported diaspores, and germination of ant-transported diaspores.     

A stochastic model of seed dispersal pattern to assess seed predation by ants in annual dry grasslands

A combined field experiment and modelling approach has been used to provide evidence that ants may be responsible for an observed lower patchiness and higher plant diversity in the neighbourhood of ant nests, within Mediterranean dry grasslands belonging to the phytosociological class Tuberarietea guttatae. The hypothesis was that seeds occurring in clumps may have a higher probability to be harvested than seeds having a scattered distribution. In order to test this hypothesis, four analysis steps were performed. First, pattern of seed production and dispersal of four species was recorded; two of them were more abundant next to ant nests (Tuberaria guttata, Euphorbia exigua), whereas the other two were more abundant away from ant nests (Bromus scoparius and Plantago bellardi). Second, a stochastic model was developed to simulate the observed dispersal patterns of each studied species. Third, 10 seed spatial arrangements in accordance to the distribution patterns created by the model were offered to ants and the location of predated seeds was recorded. Finally, the observed pattern of seed predation was matched to models performed by different distributions of probability. Results showed that the probability of being predated decreased as distance among seeds increased. This preference of ants for high concentration of food items holds down the dominant species sufficiently to allow the subordinates to survive, thus increasing diversity near nests. The observed higher frequency of small-seeded, small-sized, or creeping therophytes close to the ant nests can be therefore seen as an example of indirect myrmecophily.     

Dropping rates of elaiosome-bearing seeds during transport by ants (Formica polyctena Foerst.): Implications for distance dispersal

In a deciduous forest, foraging ants collect elaiosome-bearing seeds and carry them to their nests. Some of the seeds reach the nest and are concentrated there. Others may be dropped by ants during transport. The dropped seeds enter the soil seed pool. However, they might be repeatedly removed by other ant individuals and carried again in the direction of the nest. Rates of seed dropping and repeated removals must be known to evaluate the effect of ant workers on dispersal distance of seeds. The rate of seed dropping is predicted to depend on size of seeds and of elaiosomes, both of which vary among plant species, and on the size of the ant workers. Mark-recapture experiments were used to evaluate dropping rates of seeds of five myrmecochorous and diplochorous plants (Chelidonium majus L., Asarum europaeum L., Viola matutina Klok., V. mirabilis L., V. hirta L.) during their transport by the ant Formica polyctena Foerst. In the series of species A. europaeum – V. hirta – V. mirabilis – Ch. majus – V. matutina, the dropping rate increased. Small workers dropped seeds of A. europaeum more often than did large ones, while seeds of V. hirta were dropped by ants of different size classes with the same frequency. Across species, dropping rates of seeds were negatively correlated with the rate at which ants removed them from the depot. The number of seeds which reach the nests is the other important parameter of seed dispersal. This parameter depends on dropping rates: seeds with lower dropping rates have higher chances of being deposited in nests. Diplochores usually produce many small seeds, which are characterised by low removal rates and high dropping rates during transport by ants. Obligate myrmecochores produce rather few large seeds, which have high removal rates and low dropping rates. To analyse the significance of seed dropping in the dispersal distance of seeds, a computer simulation based on two factors [(i) seed number produced by a plant; (ii) dropping rate of seeds] is proposed.     

Predaceous ants, beach replenishment, and nest placement by sea turtles

Ants known for attacking and killing hatchling birds and reptiles include the red imported fire ant (Solenopsis invicta Buren), tropical fire ant [Solenopsis geminata (Fabr.)], and little fire ant [Wasmannia auropunctata (Roger)]. We tested whether sea turtle nest placement influenced exposure to predaceous ants. In 2000 and 2001, we surveyed ants along a Florida beach where green turtles (Chelonia mydas L.), leatherbacks (Dermochelys coriacea Vandelli), and loggerheads (Caretta caretta L.) nest. Part of the beach was artificially replenished between our two surveys. As a result, mean beach width experienced by nesting turtles differed greatly between the two nesting seasons. We surveyed 1,548 sea turtle nests (2000: 909 nests; 2001: 639 nests) and found 22 ant species. S. invicta was by far the most common species (on 431 nests); S. geminata and W. auropunctata were uncommon (on 3 and 16 nests, respectively). In 2000, 62.5% of nests had ants present (35.9% with S. invicta), but in 2001, only 30.5% of the nests had ants present (16.4% with S. invicta). Turtle nests closer to dune vegetation had significantly greater exposure to ants. Differences in ant presence on turtle nests between years and among turtle species were closely related to differences in nest placement relative to dune vegetation. Beach replenishment significantly lowered exposure of nests to ants because on the wider beaches turtles nested farther from the dune vegetation. Selective pressures on nesting sea turtles are altered both by the presence of predaceous ants and the practice of beach replenishment.     

Seasonally different modes of seed dispersal in the prostrate annual, <Emphasis Type="Italic">Chamaesyce maculata</Emphasis> (L.) Small (Euphorbiaceae), with multiple overlapping generations

The modes of seed dispersal in the prostrate annual, Chamaesyce maculata, with multiple overlapping generations were investigated. We found that C. maculata has two modes of seed dispersal; autochory in the summer and myrmecochory in the autumn. Seasonally different modes of seed dispersal have not been known in other plant species. The large proportion of seeds produced in the summer was positioned further than the expanse of the parent plants by automatic mechanical seed dispersal. Therefore, autochory would be effective for avoiding competition between parent and offspring plants. No autochory occurred in the seeds produced in the autumn. The seeds of C. maculata without an elaiosome were dispersed by seed-collecting ants in the autumn. Although 18 ant species in total visited the plants of C. maculata at the 50 sites investigated, only two ant species, Tetramorium tsushimae and Pheidole noda frequently carried the seeds of C. maculata. The low frequency of seeds carried out of the nest by P. noda suggests that the workers of P. noda carry the seeds as food into their nest. So, P. noda might be a less effective seed disperser for C. maculata, corresponding to the effectiveness of seed dispersal by harvester ants. However, T. tsushimae ants frequently carried the seeds into and out of their nest, suggesting that T. tsushimae do not regard the seeds of C. maculata as a food resource. Thus, T. tsushimae may be an effective seed disperser for C. maculata.     

Ant-seed interactions: combined effects of ant and plant species on seed removal patterns

Seed dispersal by ants (i.e. myrmecochory) is usually considered as a mutualism: ants feed on nutritive bodies, called elaiosomes, before rejecting and dispersing seeds in their nest surroundings. While mechanisms of plant dispersal in the field are well documented, the behaviour of the ant partner was rarely investigated in details. Here, we compared in laboratory conditions the foraging behaviour of two ant species, the omnivorous Lasius niger and the insectivorous Myrmica rubra to which seeds of two European myrmecochorous plants (Chelidonium majus and Viola odorata) were given. Ant colonies were simultaneously presented three types of items: entire seeds with elaiosome (SE), seeds without elaiosome (S) and detached elaiosomes (E). The presence of elaiosomes on seeds did not attract workers from a distance since ants first contact equally each type of items. Although ants are mass-recruiting species, we never observed any recruitment nor trail-laying behaviour towards seeds. For ants having contacted seed items, their antennation, manipulation and seed retrieval behaviour strongly varied depending on the species of each partner. Antennation behaviour, followed by a loss of contact, was the most frequent ant-seed interaction and can be considered as a “hesitation” clue. For both plant species, insectivorous Myrmica ants removed items in larger number and at higher speed than Lasius. This fits with the hypothesis of a convergence between odours of elaiosomes and insect preys. For both ant species, the small Chelidonium seeds were retrieved in higher proportion than Viola ones, confirming the hypothesis that ants prefer the higher elaiosome/diaspore-ratio. Thus, in these crossed experiments, the ant-plant pair Myrmica/Chelidonium was the most effective as ants removed quickly almost all items after a few antennations. The presence of an elaiosome body increased the seed removal by ants excepting for Myrmica which retrieved all Chelidonium seeds, even those deprived of their elaiosome. After 24 h, all the retrieved seeds were rejected out of the nest to the refuse piles. In at least half of these rejected items, the elaiosome was discarded by ants. Species-specific patterns and behavioural differences in the dynamics of myrmecochory are discussed at the light of ant ecology. Received 10 September 2007; revised 5 February 2008; accepted 5 March 2008.     

Are subordinate ants the best seed dispersers? Linking dominance hierarchies and seed dispersal ability in myrmecochory interactions

True myrmecochory involves the dispersal of elaiosome-bearing seeds by ants. Between the guild of ants that are attracted to these seeds, only a few of them will act as effective dispersers, that is, transporting the seeds to suitable sites (the nests) for germination and plant establishment. Ant communities are known to be highly hierarchical, and subordinate ants quickly deliver resources to their nest rather than consuming it on-site, thereby avoiding encounters with more dominant species. As a result of a series of studies that were carried out during summer in semi-arid Northwest Argentina, we have found that the most important seed disperser of the myrmecochorous plant Jatropha excisa Griseb. (Euphorbiaceae), the ant Pogonomyrmex cunicularius pencosensis Forel, was the most subordinate species during interspecific interactions. The daily timing of release of the J. excisa seeds through ballistic dispersal increased their probability of being removed by the highly thermophilic P. cunicularius pencosensis. Foraging during the warmest hours of the day allowed P. cunicularius pencosensis ants to avoid the risk of interference competition with dominant species, which also behaved as elaiosome predators. As a conclusion, subordinance behaviour appears to be integral to successful myrmecochory, and also the timing of seed release plays a key role in shaping the dynamics of myrmecochorous interactions. Therefore, ant-dispersed plants should not only favour their discovery by subordinate ants, but also should present their seeds at those times of the day when the behaviourally dominant ants are less active.     

Preferential removal of non-injured seeds by an omnivorous ant,Tetramorium tsushimae Emery,in the seed dispersal of Chamaesyce maculata (L.) small

To elucidate roles of an omnivorous ant, Tetramorium tsushimae Emery, against pre-dispersal seed consumers in the seed dispersal of Chamaesyce maculata (L.) Small, the effects of the seed injury by a stinkbug, Nysius plebeius Distat, on the seed removal by the ant and the germination rate were examined in laboratory experiments. The ants of T. tsushimae removed more frequently non-injured seeds than injured seeds. Therefore, low removal frequency of injured seeds by T. tsushimae ants might facilitate the increase in removal frequency of non-injured seeds, consequently leading to efficient seed dispersal of C. maculata. The germination rate of injured seeds that N. plebeius nymphs sucked was conspicuously lower than the non-injured seeds. The germination rate of seeds that T. tsushimae ants carried out of their nest was similar to that of the non-injured seeds. Thus, seed removal by T. tsushimae ants has hardly effects on the germination of these seeds. Therefore, the preferential removal of non-injured seeds by T. tsushimae ants might contribute to the dispersal success of C. maculata seeds. These results might show a novel interaction between myrmecochorous plants and ants in which the assessment of seed quality by ants contributes to the reproductive success of plants.     

Unexpected relationships and valuable mistakes: non‐myrmecochorous Prosopis dispersed by messy leafcutting ants in harvesting their seeds

Abstract Ants generally disperse seeds while feeding on fruits or structures attached to the seed. Seed dispersal as a by‐product of seed predation (dyszoochory) was recognized in specialized harvester ants, but not in ants predating seeds opportunistically. Leafcutting ants are the main herbivores in much of the Neotropics, and they have been reported to remove fruits and seeds, but their role as seed predators and dispersers has not been acknowledged. Prosopis flexuosa D.C. (Fabaceae, Mimosoideae) is the most abundant tree species in the central Monte Desert, Argentina, and it is likely to depend on secondary animal dispersal. Mammalian frugivores are usually considered its main dispersers, but the opportunity for dispersal may be small since the removal of fruits and seeds by seed predators is very intense. The objective of this study was to identify which ant species interact with P. flexuosa fruits and to evaluate their relative importance as seed predators and dispersers. In a field experiment, whole and segmented pods were offered and several ant species exploiting the fruits were identified. Additionally, all pod segments remaining around nests of the three ant species able to remove them (the leafcutters Acromyrmex lobicornis Emery and Acromyrmex striatus Roger, and Pheidole bergi Mayr) were examined during and after the P. flexuosa primary dispersal season. Up to 753 pod segments and 90 sound seeds were found accumulated in a circle of 1 m radius over nests of A. lobicornis, and even more in an examined trail. Acromyrmex striatus left a smaller proportion of sound seeds and P. bergi left a smaller number of pod segments. All tendencies were similar during shorter known periods of accumulation. Leafcutting ants are acting as important seed predators, and ‘by mistake’ may be dispersing a key non‐myrmecochorous tree. This is an unexplored path in the seed dispersal cycle of P. flexuosa that challenges the tendency to predict interactions based on classifications made with other goals.     

Impact of seed abundance on seed processing and dispersal by the red ant Myrmica rubra

1. Myrmecochory sensu stricto is an ant–plant mutualism in which non‐granivorous ants disperse plant diaspores after feeding on their nutrient‐rich seed appendage, the elaiosome. Phenological traits associated with the diaspore can influence the behaviour of ants and thus their ultimate efficiency as seed dispersers. 2. This study investigated how a contrasting availability of seeds (20 vs. 200 seeds) from the diplochorous Chelidonium majus (Papaveraceae, Linnaeus) plant species influences the behaviour of Myrmica rubra (Formicidae, Linnaeus) ants, from the retrieval of seeds until their dispersal outside the ant nest. 3. Regardless of seed abundance, the ants collected the first diaspores at similar rates. Then, seed retrieval sped up over time for large seed sources until satiation took place with only one‐third of the tested colonies wholly depleting abundant seed sources. 4. No active recruitment by trail‐laying ants was triggered, even to an abundant seed source 5. In both conditions of seed abundance, the majority of the diaspores retrieved inside the nest were discarded with the elaiosome removed and were dispersed at similar distances from the nest. 6. The paper concludes with a discussion of how the quantity of seeds released by a plant with a dual mode of dispersal can potentially influence the behaviour of ant dispersers and hence the dispersal efficiency derived from myrmecochory.