Parasitoids and competitors influence colony-level responses in the red imported fire ant,<Emphasis Type="Italic"> Solenopsis invicta</Emphasis>

Social insect colonies respond to challenges set by a variable environment by reallocating work among colony members. In many social insects, such colony-level task allocation strategies are achieved through individual decisions that produce a self-organized adapting group. We investigated colony responses to parasitoids and native ant competitors in the red imported fire ant (Solenopsis invicta). Parasitoid flies affected fire ants by decreasing the proportion of workers engaged in foraging. Competitors also altered colony-level behaviours by reducing the proportion of foraging ants and by increasing the proportion of roaming majors, whose role is colony defence. Interestingly, the presence of both parasitism and competition almost always had similar effects on task allocation in comparison to each of the biotic factors on its own. Thus, our study uniquely demonstrates that the interactive effect of both parasitism and competition is not necessarily additive, implying that these biotic factors alter colony behaviour in distinct ways. More generally, our work demonstrates the importance of studying the dynamics of species interactions in a broader context.     

In-nest environment modulates nestmate recognition in the ant<Emphasis Type="Italic"> Camponotus fellah</Emphasis>

Multiple behavioral and chemical studies indicate that ant nestmate recognition cues are low-volatile substances, in particular hydrocarbons (HCs) located on the cuticular surface. We tested the hypothesis that in the ant Camponotus fellah, nest environment, in particular nest volatile odors, can modulate nestmate-recognition-mediated aggression. Workers were individually confined within their own nest in small cages having either a single mesh (SM = limited physical contact permitted) or a double mesh (DM = exposed to nest volatiles only) screen. Individual workers completely isolated outside their nest (CI) served as control. When reintroduced into a group of 50 nestmates, the CI workers were attacked as alien ants after only 2 weeks of separation, whereas the SM workers were treated as nestmates even after 2 months of separation. Aggression towards DM ants depended on the period of isolation. Only DM workers isolated for over 2 months were aggressed by their nestmates, which did not significantly differ from the CI nestmates. Cuticular HC analyses revealed that the profile of the non-isolated ants (NI) was clearly distinct from that of CI, SM and DM ants. Profile differences matched the aggressive response in the case of CI ants but were uncorrelated in the case of SM or DM ants. This suggests that keeping the ants within the nest environment affected nestmate recognition in additional ways than merely altering their HC profile. Nest environment thus appears to affect label–template mismatch by modulating aggressive behavior, as well as the direction at which cuticular HCs diverged during the separation period.     

Application of the ‘Climafor’ Approach to Estimate Baseline Carbon Emissions of a Forest Conservation Project in the Selva Lacandona,Chiapas, Mexico

We present a methodology for testing and applying a regional baseline for carbon (C) emissions from land-use change, using a spatial modelling approach (hereafter called the Climafor approach). The methodology is based on an analysis of causal factors of previous land-use change (Castillo et al. 2005). Carbon risk matrices constructed from the spatial correlation analysis between observed deforestation and driving factors (Castillo et al. 2005), are used to estimate future carbonemissions within acceptable limits for a forest conservation project. The performance of two risk matrices were tested by estimating carbon emissions between 1975 and 1996 from randomly selected sample plots of sizes varying from 1,600 to 10,000 ha and comparing the results of the observed emissions from these sample plots with the model estimations. Expected emissions from continued land-use change was estimated for the community applying the risk matrices to the current land cover. The methodology provides an objective means of constructing baseline scenarios including confidence intervals, using the sum of variances of the various data sources, such as measured carbon densities, classification errors, errors in the risk matrices, and differences between the model prediction and observed emissions of sample plots due to sample size. The procedures applied in this study also give an indication of the impact of the variance in the various data sources on the size of the confidence intervals, which allows project developers to decide what data sources are essential to improve his baseline. The modelling approach to estimate the deforestation pattern is based on readily available cartographic and census data, whereas data on carbon densities are required to assess the potential for forest conservation projects to offset carbon emissions.     

Light-dependent magnetoreception in birds: interaction of at least two different receptors

Passerine migrants require light from the blue-green part of the spectrum for magnetic compass orientation; under yellow light, they are disoriented. European robins tested under a combination of yellow light and blue or green light showed a change in behavior, no longer preferring their seasonally appropriate migratory direction: in spring as well as in autumn, they preferred southerly headings under blue-and-yellow and northerly headings under green-and-yellow light. This clearly shows that yellow light is not neutral and suggests the involvement of at least two types of receptors in obtaining magnetic compass information, with the specific interaction of these receptors being rather complex.     

Oviposition strategies of conifer seed chalcids in relation to host phenology

Insects are considered the most important predators of seed cones, the female reproductive structures of conifers, prior to seed dispersal. Slightly more than 100 genera of insects are known to parasitize conifer seed cones. The most diverse (i.e., number of species) of these genera is Megastigmus (Hymenoptera: Torymidae), which comprises many important seed pests of native and exotic conifers. Seed chalcids, Megastigmus spp., lay eggs inside the developing ovules of host conifers and, until recently, oviposition was believed to occur only in fertilized ovules. Ovule development begins just after pollination, but stops if cells are not fertilized. The morphological stage of cone development at the time of oviposition by seed chalcids has been established for many species; however, knowledge of ovule development at that time has been documented for only one species, M. spermotrophus. Megastigmus spermotrophus oviposits in Douglas-fir ovules after pollination but before fertilization. Unlike the unfertilized ovules, those containing a M. spermotrophus larva continue to develop, whether fertilized or not, stressing the need to broaden our understanding of the insect–plant interactions for this entire genus. To achieve this task, we reviewed the scientific literature and assembled information pertaining to the timing of oviposition and to the pollination and fertilization periods of their respective host(s). More specifically, we were searching for circumstantial evidence that other species of Megastigmus associated with conifers could behave (i.e., oviposit before ovule fertilization) and impact on female gametophyte (i.e., prevent abortion) like M. spermotrophus. The evidence from our compilation suggests that seed chalcids infesting Pinaceae may also oviposit before ovule fertilization, just like M. spermotrophus, whereas those infesting Cupressaceae seemingly oviposit after ovule fertilization. Based on this evidence, we hypothesize that all species of Megastigmus associated with Pinaceae can oviposit in unfertilized ovules, whereas those exploiting Cupressaceae cannot, and thus oviposit only in already fully developed fertilized seeds. Furthermore, we predict that the presence of a larva in unfertilized ovules of all Pinaceae will influence the development of the female gametophyte by preventing its abortion. This influence on the Pinaceae can be interpreted as an ability to parasitize any of the potential seeds present in a seed cone, and as such represents a much more efficient oviposition strategy than searching and locating only fertilized seeds. Concomitantly, this ability has likely led to an overestimation of the impact of the species of seed chalcid infesting Pinaceae on seed production.     

Miocene to recent history of the western Altiplano in northern Chile revealed by lacustrine sediments of the Lauca basin (18°15′–18°40′ S/69°30′–69°05′W)

The intramontane Lauca Basin at the western margin of the northern Chilean Altiplano lies to the west of and is topographically isolated from the well-known Plio-Pleistocene lake system of fluvio-lacustrine origin that covers the Bolivian Altiplano from Lake Titicaca to the north for more than 800?km to the Salar de Uyuni in the south. The Lauca Basin is filled by a sequence of some 120?m of mainly upper Miocene to Pliocene clastic and volcaniclastic sediments of lacustrine and alluvial origin. Volcanic rocks, partly pyroclastic, provide useful marker horizons. In the first period (6–4?Ma) of its evolution, the 'Lago Lauca' was a shallow ephemeral lake. Evaporites indicate temporarily closed conditions. After 4?Ma the lake changed to a perennial water body surrounded by alluvial plains. In the late Pleistocene and Holocene (2–0?Ma) there was only marginal deposition of alluvial and glacial sediments. The basin formed as a half-graben or by pull-apart between 10 and 15?Ma (tectonic displacement of the basal ignimbrite sequence during the 'Quechua Phase') and 6.2?Ma (maximum K/Ar ages of biotites of tuff horizons in the deepest part of the basin). Apart from this early basin formation, there has been surprisingly little displacement during the past 6?Ma close to the Western Cordillera of the Altiplano. Also, climate indicators (pollen, evaporites, sedimentary facies) suggest that an arid climate has existed for the past 6?Ma on the Altiplano. Together, these pieces of evidence indicate the absence of large scale block-faulting, tilt and major uplift during the past 5–6?Ma in this area.