No abstract

How do termite inquilines manage to cohabit termitaria along with the termite builder species? With this in mind, we analysed one of the several strategies that inquilines could use to circumvent conflicts with their hosts, namely, the use of distinct diets. We inspected overlapping patterns for the diets of several cohabiting Neotropical termite species, as inferred from carbon and nitrogen isotopic signatures for termite individuals. Cohabitant communities from distinct termitaria presented overlapping diet spaces, indicating that they exploited similar diets at the regional scale. When such communities were split into their components, full diet segregation could be observed between builders and inquilines, at regional (environment-wide) and local (termitarium) scales. Additionally, diet segregation among inquilines themselves was also observed in the vast majority of inspected termitaria. Inquiline species distribution among termitaria was not random. Environmental-wide diet similarity, coupled with local diet segregation and deterministic inquiline distribution, could denounce interactions for feeding resources. However, inquilines and builders not sharing the same termitarium, and thus not subject to potential conflicts, still exhibited distinct diets. Moreover, the areas of the builder’s diet space and that of its inquilines did not correlate negatively. Accordingly, the diet areas of builders which hosted inquilines were in average as large as the areas of builders hosting no inquilines. Such results indicate the possibility that dietary partitioning by these cohabiting termites was not majorly driven by current interactive constraints. Rather, it seems to be a result of traits previously fixed in the evolutionary past of cohabitants.

No abstract

Inter-specific symbiotic links are often reinforced by morphological, physiological, or behavioural trait modification undergone by the associated species. In some cases, such as in physogastric termitophile staphylinids, such modifications do facilitate the social interaction. Here we inspect chemical traits of the physogastric staphylinid Corotoca melantho (Insecta: Coleoptera) and its termite host Constrictotermes cyphergaster (Insecta: Blattodea: Isoptera), aiming to verify whether staphylinids resemble their host. First, we compared CHC profiles of hosts and guests within and among termitaria, to gather evidence on the origin of such profiles in guests. Then, we examined nitrogen and carbon isotopic signatures of these cohabitants to inspect whether chemical disguise is achieved by predation of host workers by staphylinids. Beetles presented CHC more similar to the CHC of their cohabiting termites than to (i) their conspecifics and (ii) termites from another nest, thereby favouring the hypothesis on CHC acquisition by guests. Isotopic signatures revealed that such similarities could not be majorly determined by share nutrition between these cohabitants. In general, our results evidenced that chemical disguise in termitophiles may function as a strategy for social integration in morphological mimics.

Structural and functional traits of organisms are known to be related to the size of individuals and to the size of their colonies when they belong to one. Among such traits, propensity to inquilinism in termites is known to relate positively to colony size. Larger termitaria hold larger diversity of facultative inquilines than smaller nests, whereas obligate inquilines seem unable to settle in nests smaller than a threshold volume. Respective underlying mechanisms, however, remain hypothetical. Here we test one of such hypotheses, namely, that nest defence correlates negatively to nest volume in Constrictotermes cyphergaster termites (Termitidae: Nasutitermitinae). As a surrogate to defence, we used ‘patrolling rate’, i.e., the number of termite individuals attending per unit time an experimentally damaged spot on the outer wall of their termitaria. We found that patrolling rate decayed allometrically with increasing nest size. Conspicuously higher patrolling rates occurred in smaller nests, while conspicuously lower rates occurred in larger nests presenting volumes in the vicinity of the threshold value for the establishment of inquilinism. This could be proven adaptive for the host and guest. At younger nest age, host colonies are smaller and presumably more vulnerable and unstable. Enhanced defence rates may, hence, prevent eventual risks to hosts from inquilinism at the same time that it prevents inquilines to settle in a still unstable nest. Conversely, when colonies grow and maturate enough to stand threats, they would invest in priorities other than active defence, opening an opportunity for inquilines to settle in nests which are more suitable or less risky. Under this two-fold process, cohabitation between host and inquiline could readily stabilize.

No abstract

1. Resource density can regulate the area that animals use. At low resource density, there is a conflict in terms of balance between costs of foraging and benefits acquired. The foraging of the higher termite Nasutitermes aff. coxipoensis consists of searching throughout trails and a building galleries phase.2. In this study, a manipulative field experiment was used to test the hypothesis that colonies of N. aff. coxipoensis forage towards a more profitable balance between the establishment of trails and gallery construction at low resource density.3. The experiment was conducted in north-eastern Brazil. Seven experimental plots were established with a continuous increase in resource density (sugarcane baits). Entire colonies of N. aff. coxipoensis were transplanted from their original sites to the experimental plot, totalling 35 nests. The number, branches and total length of trails and galleries were quantified.4. The results show that N. aff. coxipoensis optimises its foraging output, intensifying the establishment of trails at the cost of gallery construction when resource density is low. The number of trails, the number of trail branches and the total length of trails decreased with increasing resource density. Interestingly, at low resource density, the search effort was concentrated on forming longer and a greater number of trails, a small proportion of which were converted into galleries. The opposite relationship was observed at high resource density. 5. These results suggest an optimisation of search efforts during foraging depending on resource density, a mechanism that may help researchers to understand the use of space by higher termite species.

Resource can regulate animal foraging range, which in turn determines the chances of species co-occurrence. Here, we addressed the question of whether resource determines the co-occurrence of soil-forager termite species (i.e. those foraging in subterranean tunnels). Eight quadrats (4 × 4 m) were marked in seven sites of Brazilian Atlantic rainforests, giving a total area sampled of 896 m 2 . Inside each quadrat, we measured the co-occurrence of soil forager species and the resource suitability (N:C ratio of the soil and litter biomass). The number of records of more than one soil-forager termite species at a single foraging spot, relative to the total number of foraging spots detected in each forest, was taken as a surrogate for spatial co-occurrence. We tested whether termite co-occurrence was mediated by random or nonrandom processes. Data were subjected to linear regression to test how the termite species co-occurrence responds to resources. We compared this method with a null model analysis. Soil-forager termites comprised 885 records, 20 species and 14 genera. From those records, 29% indicated species co-occurrence. Co-occurrence was not random: occurred more frequently when resource suitability was very high or very low. This result suggests an optimised use of space by termite communities.