Incident daylight as orientation cue for hole-boring ants: prostomata in Macaranga ant-plants (original) (raw)
Related papers
Insectes Sociaux, 1998
In the tropical peat swamp forests of South-East Asia, the ant-plant Macaranga puncticulata is specifically associated with Camponotus (Colobopsis) sp. 1 (Formicidae: Formicinae), a member of the C. saundersi-group. This ant shows a variety of adaptations to its plant-bound mode of life. The queens are capable of locating young M. puncticulata plants inside the forest and of chewing entrance holes into the domatia by themselves. C. (Colobopsis) sp. 1 nests were found exclusively inside the domatia of M. puncticulata. The diet consisted predominantly of host plant resources (food bodies and extrafloral nectar), but insect prey were taken too. In contrast to all the other obligate ant associates of Macaranga, C. (Colobopsis) sp. 1 never cultivated any scale insects. Nevertheless, tending Homoptera ("trophobiosis") is indeed included in the behavioral repertoire, but the ants showed this capacity only in experiments in which the host plants had been completely deprived of extrafloral nectaries. Large C. (Colobopsis) sp.1 colonies are polydomous and can extend over up to 20 M. puncticulata trees. There is strong intraspecific competition for host plants during several stages of the colony development. We observed conspicuous pushing fights between queens that tried to found colonies on the same young plant. C. (Colobopsis) sp.1 workers were capable of removing water from flooded domatium chambers. They quickly gathered around fresh injuries to M. puncticulata. Herbivorous insects were fiercely attacked and either driven away from the plant or captured as prey. Moreover, workers often pruned vines that came into contact with their host trees. We could show that colonization by C. (Colobopsis) sp.1 is beneficial for M. puncticulata, since the ants effectively reduced herbivory and plant competition.
Host plant protection by arboreal ants: looking for a pattern in locally induced responses
Evolutionary Ecology Research, 2008
Background: Among arboreal ants, both territorially dominant species and plant-ants (e.g. species associated with myrmecophytes or plants housing them in hollow structures) protect their host trees against defoliators. Yet, locally induced responses, or the recruitment of nest-mates when a worker discovers a wound on its host-tree, were only noted in plant-ants. We wondered whether this might be due to the examination of the phenomenon being restricted to only six plant-ant species belonging to four genera. Based on the ant genus Azteca, a Neotropical group of arboreal species, we compared five species. The territorially dominant, carton-nester A. chartifex, three plant-ant species [A. alfari and A. ovaticeps associated with myrmecophitic Cecropia (Cecropiaceae), and A. bequaerti associated with Tococa guianensis (Melastomataceae)], and A. schimperi thought to be a temporary social parasite of true Cecropia ants. Methods: We artificially inflicted wounds to the foliage of the host tree of the different ant species. We then compared the number of workers on wounded versus control leaves. Results: We noted a locally induced response in the three plant-ant species as well as in the territorially dominant species, but very slightly so in A. schimperi.
Parenchyma: a neglected plant tissue in the Cecropia/ant mutualism
Symbiosis, 2011
The Cecropia/Azteca association is a well studied and perhaps the best known mutualistic system in the Neotropics. In this study we assessed the ultrastructure of the parenchymal tissue of the septum inside the internodes of two Cecropia species, Cecropia obtusifolia (a myrmecophytic species) and C. angustifolia (a non-myrmecophytic species), through the use of scanning electron microscopy. We found a series of large oval cavities in the parenchyma of C. obtusifolia, which were absent in the parenchyma of C. angustifolia, and which seemed to be spatially associated with vascular bundles. We also found two layers of fibers in C. obtusifolia, one on each side of the septum. Finally, the parenchymal cells of C. angustifolia were filled with several tiny oval bodies, which appeared to be plastids (perhaps serving as storage) and which were completely absent in C. obtusifolia. The structural differences between these two Cecropia species, as well as other evidence from the behavior of the ants, suggests that the parenchyma of myrmecophytic Cecropia species provides an additional source of nutrition for the Azteca queens during colonization of Cecropia saplings. Other possible uses of parenchymal tissue by the ant colony are also discussed.
Evolution, 2004
We investigate the evolution of host association in a cryptic complex of mutualistic Crematogaster (Decacrema) ants that inhabits and defends Macaranga trees in Southeast Asia. Previous phylogenetic studies based on limited samplings of Decacrema present conflicting reconstructions of the evolutionary history of the association, inferring both cospeciation and the predominance of host shifts. We use cytochrome oxidase I (COI) to reconstruct phylogenetic relationships in a comprehensive sampling of the Decacrema inhabitants of Macaranga. Using a published Macaranga phylogeny, we test whether the ants and plants have cospeciated. The COI phylogeny reveals 10 wellsupported lineages and an absence of cospeciation. Host shifts, however, have been constrained by stem traits that are themselves correlated with Macaranga phylogeny. Earlier lineages of Decacrema exclusively inhabit waxy stems, a basal state in the Pachystemon clade within Macaranga, whereas younger species of Pachystemon, characterized by nonwaxy stems, are inhabited only by younger lineages of Decacrema. Despite the absence of cospeciation, the correlated succession of stem texture in both phylogenies suggests that Decacrema and Pachystemon have diversified in association, or codiversified. Subsequent to the colonization of the Pachystemon clade, Decacrema expanded onto a second clade within Macaranga, inducing the development of myrmecophytism in the Pruinosae group. Confinement to the aseasonal wet climate zone of western Malesia suggests myrmecophytic Macaranga are no older than the wet forest community in Southeast Asia, estimated to be about 20 million years old (early Miocene). Our calculation of COI divergence rates from several published arthropod studies that relied on tenable calibrations indicates a generally conserved rate of approximately 1.5% per million years. Applying this rate to a rate-smoothed Bayesian chronogram of the ants, the Decacrema from Macaranga are inferred to be at least 12 million years old (mid-Miocene). However, using the extremes of rate variation in COI produces an age as recent as 6 million years. Our inferred timeline based on 1.5% per million years concurs with independent biogeographical events in the region reconstructed from palynological data, thus suggesting that the evolutionary histories of Decacrema and their Pachystemon hosts have been contemporaneous since the mid-Miocene. The evolution of myrmecophytism enabled Macaranga to radiate into enemyfree space, while the ants' diversification has been shaped by stem traits, host specialization, and geographic factors. We discuss the possibility that the ancient and exclusive association between Decacrema and Macaranga was facilitated by an impoverished diversity of myrmecophytes and phytoecious (obligately plant inhabiting) ants in the region.
Hundreds of tropical plant species house ant colonies in specialized chambers called domatia. When, in 1873, Richard Spruce likened plant-ants to fleas and asserted that domatia are ant-created galls, he incited a debate that lasted almost a century. Although we now know that domatia are not galls and that most ant-plant interactions are mutualisms and not parasitisms, we revisit Spruce’s suggestion that ants can gall in light of our observations of the plant-ant Myrmelachista schumanni, which creates clearings in the Amazonian rain forest called “supay-chakras,” or “devil’s gardens.” We observed swollen scars on the trunks of nonmyrmecophytic canopy trees surrounding supay-chakras, and within these swellings, we found networks of cavities inhabited by M. schumanni. Here, we summarize the evidence supporting the hypothesis that M. schumanni ants make these galls, and we hypothesize that the adaptive benefit of galling is to increase the amount of nesting space available to M. schumanni colonies.
Supplemental Experimental Procedures Ant-Plant Interactions: Detailed Description
2016
We used as a reference system the interactions between ants and plants (Figure S1). Ants are a dominant part of animal biodiversity in almost all terrestrial environments, and it is therefore not surpris-ing that ant-plant interactions are geographically widespread and common in many ecological communities [S1]. Ants have been shown to be important in plant defense against herbivores, are rele-vant seed dispersers in deserts and forests, and promote selective gardening of plants (reviewed in [S1, S2]). In general, through their sheer diversity, ants have evolved a wide range of mutualistic inter-actions with plants and have evolved vary broadly in their degree of interaction intimacy [S2]. Some ant-plant mutualisms are symbiotic, such as those between myrmecophytes and their protective ants [S3]. In such cases, interacting individuals show long-term physical contact with partners during their lifespan, and the ant-plant interac-tion involves specialized structures within plant hosts...
Ant-fed plants: comparison between three geophytic myrmecophytes
Biological Journal of the Linnean Society, 2004
In their association with myrmecophytes (i.e. plants that shelter a limited number of ant species in hollow structures), ants sometimes provide only poor biotic protection for their host plants, but may supply them with nutrients (myrmecotrophy). We studied three geophytic myrmecophytes growing in the understorey of Guianian rain forests. Allomerus ants build spongy-looking galleries rich in detritus and insect debris over the stems of their host plants [ Cordia nodosa Lamark (Boraginaceae) and Hirtella physophora Martius & Zuccharini (Chrysobalanaceae)], while Pheidole minutula Mayr colonies deposit their waste in the leaf pouches of their host plant [ Maieta guianensis Aublet (Melastomataceae)]. This waste is more nitrogen-rich than that found in the Allomerus galleries, themselves containing more nitrogen than the plant leaves. Using stable isotope analysis we noted a significant difference in d 15 N between ant-occupied and unoccupied plants only for Maieta , for which 80% of the host plant nitrogen is derived from Pheidole waste. Experiments on all three plants using a 15 N-supplemented solution of NH 4 Cl confirmed these results, with an increase in this isotope noted between control and experimental plants only for Maieta. The internal surfaces of Maieta leaf pouches bear protuberances whose likely role is to absorb nutrients from the Pheidole waste. The alternative hypothesis, that these protuberances play a role in provisioning ants, was rejected after comparing their structure with those of extrafloral nectaries and food bodies in a histological study.
Sociobiology
This report elucidates the process of settlement by Coccus scale insects into Crematogaster plant-ant nests formed inside the hollow stems of a myrmecophytic species, Macaranga bancana, in a tropical rain forest. We collected wafting scale insect nymphs from the canopy using sticky traps and characterized the DNA sequence of the trapped nymphs. In addition, we experimentally introduced first-instar nymphs of both symbiotic and nonsymbiotic scale insects to M. bancana seedlings with newly formed plant-ant colonies. Nymphs of symbiotic species were generally carried by ants into their nests within a few minutes of introduction. Most nymphs of nonsymbiotic species were thrown to the ground by ants. Our results suggest that in Crematogaster–Macaranga myrmecophytism, symbiotic coccids disperse by wind onto host plant seedlings at the nymphal stage, and plant-ants actively carry the nymphs landing on seedlings into their nests in discrimination from nonsymbiotic scale insects.
Finding its place in a competitive ant community: leaf fidelity of Camponotus sericeus
Insectes Sociaux, 2003
Many species of ground nesting ants regularly visit extrafloral nectaries (EFNs) of the savannah tree Pseudocedrela kotschyi. The distribution of ants on the plants is mosaic-like, i. e. stable and predictable with different ant species dominating neighbouring trees. In order to examine whether foraging behaviour may influence the structure of these ant communities, we investigated individual foraging behaviour of Camponotus sericeus, the ant species with highest incidence on P. kotschyi trees in the study area. Foragers of C. sericeus continuously visited EFNs on the leafs of P. kotschyi during their diurnal activity period. Individually marked foragers showed a pronounced fidelity for individual plants and particular leaves. Ant individuals returned to the same plants over a three week period at least. They persistently focused foraging on the same leaves (about three per ant). Null model analysis of ant distribution revealed that ants partitioned their host plant. Co-occurrence on the same leaves was significantly lower than could be expected by chance for most trees studied. Foraging was not oriented towards the plants growing closest to the nest but more distantly growing plants were considerably used. Choice of plants could therefore be influenced by plant quality or by presence of other, competing ant species. The study is the first to show leaf fidelity caused by EFNs and micro-site fidelity within the context of species rich ant communities. It considers the resulting systematic, partitioned use of individual plants as important factor supporting the formation of a mosaic-like ant distribution on plants.