Fig pollinators (Agaonidae, Chalcioidea) lay their eggs in fig inflorescences (Ficus, Moraceae). Reproductive success for both partners is thus largely dependent on the dispersal of these tiny wasps. Some are known to cover substantial distances (> 10 km) using wind above the canopy. However, fig ecology is extremely varied, and hence one might also expect a diversity of pollinator dispersal strategies. We studied fig pollinator dispersal in Sarawak (2001 and 2004) and Peninsular Malaysia (2003). The results indicate substantial differences in dispersal ecology between the pollinators of monoecious and dioecious figs. Monoecious-fig pollinators were common, and species composition and rank abundances were similar between years despite short sampling periods. Substantial temporal and spatial variation in their production is thus smoothed out by long-distance dispersal. Some species whose hosts do not occur at our Sarawak site and are rare throughout Borneo were caught, suggesting exceptionally long-distance dispersal in these species. Conversely, few dioecious-fig pollinators were caught and species overlap between years was low. Dispersal range in many dioecious-fig pollinators may be more restricted. At a finer scale, among genera pollinating monoecious figs we found marked differences in flight behaviour (height and time-of-dispersal). We relate these findings to the ecology of their hosts, and discuss the implications for fig–fig-pollinator coevolution.

The various mutualistic and antagonistic symbioses between fig trees (Ficus: Moraceae) and chalcid wasps comprise a community in microcosm. Phylogenetic estimates of figs and fig wasps show general topological correspondence, making the microcosm a model system for cophylogeny. Incongruence between phylogenies from associated organisms can be reconciled through a combination of evolutionary events. Cophylogeny mapping reconciles phylogenies by embedding an associate tree into a host tree, finding the optimal combinations of events capable of explaining incongruence and evaluating the level of codivergence. This review addresses the results of cophylogeny analysis concerning Ficus and discusses the plausibility of different evolutionary events. Five different associations encompassing fig-pollinator, fig-parasite and pollinator-parasitoid interactions are reconciled. The method improves on previous comparisons by employing ‘jungles’ to provide an exhaustive and quantitative analysis of cophylogeny. A jungle is a mechanism for inferring host switches and obtaining all potentially optimal solutions to the reconciliation problem. The results support the consensus that figs codiverge significantly with pollinators but not non-pollinators. However, pollinators still appear to have switched between hosts in contradiction to the traditional model of faithful codivergence. This emphasises the growing realisation that evolutionary transitions in the microcosm are more flexible than previously thought and host specificity is necessary but not sufficient for codivergence. The importance of sampling strategy is emphasised by the influence of taxon set on the fig-pollinator and fig-parasite jungles. Spurious significant results for fig-parasite and fig-parasitoid jungles indicate that the choice of congruence measure influences significance; the total number of events required to reconcile two trees (‘total cost’) is not a good measure of congruence when switches cannot be realistically weighted.