Can management intensity be more important than environmental factors? A case study along an extreme elevation gradient from central Italian cereal fields

This paper aims to assess the importance of environmental and management factors determining the weed species composition along a strong elevation gradient. A total of 76 cereal fields (39 low input and 37 intensively managed) were sampled along an elevation gradient in central Italy. Explanatory variables were recorded for each field to elucidate the role of large-scale spatial trends, of site-specific abiotic environmental conditions and of field management characters. Redundancy analysis was used to assess the relative importance of each environmental variable in explaining the variation in species composition. Our results indicate that variation in weed species composition is strongly determined by altitude, mean annual precipitation, mean annual temperature and also by soil characteristics. However, the level of intensification proved to be the most influential variable. There was a significant difference in species richness and composition between low-input and intensively managed fields. Intensification leads to considerable species loss at both lower and higher elevations. Low-input fields had 296 species in total, while intensively managed fields had only 196

CD28-B7 Costimulatory Blockade by CTLA4Ig Delays the Development of Retrovirus-Induced Murine AIDS

Mouse AIDS (MAIDS) induced in C57BL/6 mice by infection with a replication-defective retrovirus (Du5H) combines extensive lymphoproliferation and profound immunodeficiency. Although B cells are the main target of viral infection, recent research has focused on CD4(+) T cells, the activation of which is a key event in MAIDS induction and progression. A preliminary observation of increased expression of B7 molecules on B cells in MAIDS prompted us to address the possible involvement of the CD28/B7 costimulatory pathway in MAIDS. Mice infected with the MAIDS-inducing viral preparation were treated with murine fusion protein CTLA4Ig (3 × 50 μg/week given intraperitoneally), a competitive inhibitor of physiological CD28-B7 interactions. In CTLA4Ig-treated animals, the onset of the disease was delayed, lymphoproliferation progressed at a much slower rate than in untreated mice, and the loss of in vitro responsiveness to mitogens was reduced. Relative expression of Du5H did not differ between treated and untreated animals. These results suggest that the CD28/B7 costimulatory pathway contributes to MAIDS development