Beyond parks as monoliths: Spatially differentiating park-people relationships in the Tadoba Andhari Tiger Reserve in India

Parks represent spatially and socially heterogeneous conservation units, yet are often assessed and managed using spatially homogeneous approaches. This paper represents an effort to focus on the larger social-ecological landscapes within which protected areas are embedded, to understand why conservation succeeds and fails in different parts of the landscape. In a wildlife sanctuary in the central plains of India (Tadoba Andhari Tiger Reserve), we address: (i) how people living within and immediately outside a park differentially impact its resources and (ii) how the park differentially impacts communities living within. Using forest plots, satellite imagery and interviews, we evaluate park conservation by assessing plant diversity, land cover change, forest fragmentation, and attitudes of local communities towards conservation. We find that interior villages have a negative impact on regeneration, but there is a decline in tree species diversity, and increased forest cover change and fragmentation at the park periphery. Interior villages suffer greatly from crop and livestock depredations by wildlife and consider park rules to be unfairly devised. Yet, they affirm the importance of the park for conservation, and are willing to work with park authorities for stricter protection. Park authorities largely focus on resettlement of interior villages, when they should also pay attention to protecting the peripheral areas of the park from severe degradation by surrounding villages. In summary, we find that different parts of the park landscape face different conservation challenges. Taking into account spatial variations in the factors influencing conservation can greatly benefit the management of protected areas.     

Promotion of tissue inflammation by the immune receptor Tim-3 expressed on innate immune cells

CD4+ T helper 1 (TH1) cells are important mediators of inflammation and are regulated by numerous pathways, including the negative immune receptor Tim-3. We found that Tim-3 is constitutively expressed on cells of the innate immune system in both mice and humans, and that it can synergize with Toll-like receptors. Moreover, an antibody agonist of Tim-3 acted as an adjuvant during induced immune responses, and Tim-3 ligation induced distinct signaling events in T cells and dendritic cells; the latter finding could explain the apparent divergent functions of Tim-3 in these cell types. Thus, by virtue of differential expression on innate versus adaptive immune cells, Tim-3 can either promote or terminate TH1 immunity and may be able to influence a range of inflammatory conditions.