OPTIMIZING THE PERFORMANCE OF IRRIGATED AGRICULTURE IN EASTERN ENGLAND UNDER DIFFERENT WATER PRICING AND REGULATION STRATEGIES

Irrigation water shortage is becoming an increasingly serious problem in agricultural production. Growing pressure on water resources is leading to increasing restrictions on abstraction for irrigation and consideration of the use of economic instruments, such as increased abstraction charges and/or tradable licences, to restrict demand and encourage wiser use of water. We evaluate irrigation using selected economic, social, and environmental indicators of performance, including the value of water used for irrigation. A linear programming model is developed and used to simulate possible responses by irrigators and the impact on irrigation performance of intervention measures, namely abstraction quota restrictions and volumetric pricing that might be used to ration water and/or increase water use efficiency. Through the use of parametric programming a scenario analysis is performed to a case study in eastern England with regard to perturbations of irrigation water under alternative policy instruments.     

Triarylmethanol Host Compounds. Synthesis, Crystalline Complex Formation and X-Ray Crystal Structures of Three Inclusion Species

A variety of triarylmethanol compounds including benzo condensed and laterally substituted derivatives 1–10 have been prepared and shown to act as crystallinehosts for the inclusion of organic solvents involving protic polar, aprotic dipolar and apolar molecules. The inclusion ability is ratherhigh for aprotic dipolar solvents while protic polarcompounds are only rarely enclathrated. Host 9 is an exception, being also efficient with alcohols and amines. Compound3 displays no inclusion formation under theexperimental conditions. X-ray crystal structures of the inclusion compound 1acetone (2:1) and of two amineinclusion compounds of host 9 [9 n-propylamine(1:1), 9di-n-propylamine (1:1)] are reported showing the formation of H-bondedhost-guest associates as the common feature of supramolecular association.Supplementary data relating to this article have beendeposited with the British Library, No. SUP 82226 (10 pages).at Boston Spa, Wetherby, West Yorkshire, U.K., as Supplementary Publication.