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Large scale landscape transformation and contingent habitat loss are among the greatest threats to ecological integrity and ecosystem health. One of the mitigation approaches used to deal with these pressures is to leave interconnected corridors and nodes as remnant ecological networks (ENs) within the transformed landscape. The South African forestry industry has already allocated 500,000 ha, one-third of the plantation holdings, consisting predominantly of natural grassland, as ENs among and within timber plantations. These ENs are intended to maintain structural, compositional and functional biodiversity. However, little scientific research is available on the effectiveness of these huge ENs for biodiversity conservation and maintenance of natural ecosystem function, although initial findings are encouraging. While the local adverse effect of alien plantation trees on functional biodiversity is not in dispute, it is at the scale of the whole landscape where there is much interest in determining how effective these ENs are in maintaining the untransformed portion of the transformed landscape in a close-to-natural state. As these ENs are extensive, species beta diversity is a consideration in addition to alpha diversity. Initial findings reveal diminished ecological integrity in narrow corridors due in part to the adverse edge effect from the alien trees into the margin of the EN. Quality of the ENs is of great importance for maintaining functional diversity, with human disturbance reducing their effectiveness. First findings, and their application to the Framework for Ecosystem Service Provision, suggest that these ENs are significant for biodiversity conservation and for provision of ecosystem services. Nevertheless, still much more research is required on a greater range of taxa, and their interactions, to improve the design of these ENs for ecological and evolutionary processes.

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The desert locust (Schistocerca gregaria) has been feared agricultural pest since early civilization, with plagues documented in ancient texts. Population genetic studies of the desert locust are needed to determine genetic variation and movement pattern for efficient control of the pest. In this study, we complemented the limited available microsatellite collection for the desert locust with 34 new polymorphic and multiplexed microsatellite loci. To this aim, we screened an expressed sequence tags library and constructed a partial genomic library enriched for dinucleotide repeats to develop high-throughput and high-quality genotyping assays. We then paid particular attention to quality control and carefully validated 26 of these novel microsatellites and six previously described loci for the absence of null alleles in Western African field populations. This large panel of high-quality microsatellite markers provides new opportunity to infer dispersal rates between populations of the desert locust and help prioritize early monitoring and control. Furthermore, high potential for cross-taxa utility of markers was observed within Schistocerca genus, which includes other locust pest species, with reliable amplification achieved for at least ten of loci per species. Microsatellite markers developed from transcriptome resources were largely devoid of null alleles and were conserved across species compared with those derived from traditional genomic libraries. Accordingly, the number of highly reliable microsatellite markers was greatly improved compared with that of previous studies on Orthopteran species, and this strategy might be broadly applied in other insect species prone to null alleles. (Résumé d'auteur

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SUMMARYThe importance of metabolic rate and/or spiracle modulation for saving respiratory water is contentious. One major explanation for gas exchange pattern variation in terrestrial insects is to effect a respiratory water loss (RWL) saving. To test this, we measured the rates of CO 2 and H 2 O release (V CO2 and V H2O , respectively) in a previously unstudied, mesic cockroach, Aptera fusca, and compared gas exchange and water loss parameters among the major gas exchange patterns (continuous, cyclic, discontinuous gas exchange) at a range of temperatures. Mean V CO2 , V H2O and V H2O per unit V CO2 did not differ among the gas exchange patterns at all temperatures (P>0.09). There was no significant association between temperature and gas exchange pattern type (P=0.63). Percentage of RWL (relative to total water loss) was typically low (9.79±1.84%) and did not differ significantly among gas exchange patterns at 15°C (P=0.26). The method of estimation had a large impact on the percentage of RWL, and of the three techniques investigated (traditional, regression and hyperoxic switch), the traditional method generally performed best. In many respects, A. fusca has typical gas exchange for what might be expected from other insects studied to date (e.g. V CO2 , V H2O , RWL and cuticular water loss). However, we found for A. fusca that V H2O expressed as a function of metabolic rate was significantly higher than the expected consensus relationship for insects, suggesting it is under considerable pressure to save water. Despite this, we found no consistent evidence supporting the conclusion that transitions in pattern type yield reductions in RWL in this mesic cockroach. Supplementary material available online at