Food security concerns and the scarcity of new productive land have put productivity enhancement of degraded lands back on the political agenda. In such a context, salt-affected lands are a valuable resource that cannot be neglected nor easily abandoned even with their lower crop yields, especially in areas where significant investments have already been made in irrigation and drainage infrastructure. A review of previous studies shows a very limited number of highly variable estimates of the costs of salt-induced land degradation combined with methodological and contextual differences. Simple extrapolation suggests that the global annual cost of salt-induced land degradation in irrigated areas could be US$ 27.3 billion because of lost crop production. We present selected case studies that highlight the potential for economic and environmental benefits of taking action to remediate salt-affected lands. The findings indicate that it can be cost-effective to invest in sustainable land management in countries confronting salt-induced land degradation. Such investments in effective remediation of salt-affected lands should form part of a broader strategy for food security and be defined in national action plans. This broader strategy is required to ensure the identification and effective removal of barriers to the adoption of sustainable land management, such as perverse subsidies. Whereas reversing salt-induced land degradation would require several years, interim salinity management strategies could provide a pathway for effective remediation and further showcase the importance of reversing land degradation and the rewards of investing in sustainable land management

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Particle size dictates where aerosolized pathogens deposit in the respiratory tract, thereafter the pathogens potential to cause disease is influenced by tissue tropism, clearance kinetics and the host immunological response. This interplay brings pathogens into contact with a range of tissues spanning the respiratory tract and associated anatomical structures. In animal models, differential deposition within the respiratory tract influences infection kinetics for numerous select agents. Greater numbers of pathogens are required to infect the upper (URT) compared with the lower respiratory tract (LRT), and in comparison the URT infections are protracted with reduced mortality. Pathogenesis in the URT is characterized by infection of the URT lymphoid tissues, cervical lymphadenopathy and septicemia, closely resembling reported human infections of the URT. The olfactory, gastrointestinal, and ophthalmic systems are also infected in a pathogen-dependent manner. The relevant literature is reviewed with respect to particle size and infection of the URT in animal models and humans.

The role of the legume in the nitrogen (N) cycle was examined in grazed pastures receiving no N fertilizer of both temperate and tropical regions by simulating the fluxes of N through different processes of the cycle. The amounts of legumefixed N required to balance the cycle without invoking a drain on soil organic N reserves (i.e. no net N mineralization) was estimated to vary from 38 to 53% of the above-ground herbage N or from 20 to 31% on a dry matter (DM) basis for tropical pasture systems with a range of pasture utilization of lO-409/o. At higher pasture utilization levels of 50-70%, more typical of intensively grazed temperate pastures, the N input requirement in the absence of fertilizer N would be 57-67% of the aboveground herbage N or 35-45% DM. An examination of the role of each contributory process of recycling {viz. excreta returns, internal cycling or remobilization from senescing tissues, litter decomposition) suggests that variations in the amounts of internally cycled N would have the greatest impact on the requirement for biologically fixed N at low levels of pasture utilization (10-40<^''o), while at high pasture utilization levels of 70%, variations in the recovery of excreta-N would have a major effect on the requirement for fixed-N to balance the cycle.The amounts of biologically fixed N required to sustain a range of herbage DM yields of 3-22 t DM ha ' yr^ ' would range from 15 to Coirespondence: Richard J. Thomas, Centro iniernacional de Agricultura Tropical, Apartado Aireo 6713, Caii. Colombia, 158 kg N ha ' yr ' for tropical pastures. For intensively managed temperate pastures producing 6-15 t DM ha" ' yr " ' with a N content of 3-5''Io, a range of fixation of 120-352 kg N ha"' yr"' is required. These simulations indicate how legume contents of 20-45% of herbage DM could contribute to productive and sustainable (in terms of N) pasture systems of both temperate and tropical regions.