Fate of legume and fertilizer nitrogen-15 in a long-term cropping systems experiment

Includes bibliographical references (pages 914-915).Relying more on biological N2 fixation has been suggested as a way to meet one of the major challenges of agricultural sustainability. A 15N study was conducted to compare the fate of applied legume and fertilizer N in a long-term cropping systems experiment. Nitrogen-15-1abeled red clover (Trifolium pratense L.) and (NH4)2SO4 ere applied microplots within the low-input and conventional cropping systems of the Farming Systems Trial at the Rodale Institute Research Center in Pennsylvania. The 15SN was applied to soil and traced into corn (Zea mays L.) in 1987 and 1988. Residual 15SN was also traced into second-year spring barley (Hordeum vulgare L.). Legume and fertilizer 15SN remaining in soil was measured and loss of N was calculated by difference. More fertilizer than legume N was recovered by crops (40 vs. 17% of input), more legume than fertilizer N was retained in soil (47 vs. 17% of input), and similar amounts of N from both sources were lost from the cropping systems (39% of input) over the 2-yr period. More fertilizer than legume N was lost during the year of application (38 vs. 18% of input), but more legume than fertilizer N was lost the year after application (17 vs. 4% of input). Residual fertilizer and legume 15SN was distributed similarly among soil fractions. Soil microbial biomass was larger in the legume-based system. A larger, but not necessarily more active, soil microbial biomass was probably responsible for the greater soil N supplying capacity in the legume-based compared with fertilizer-based system

Small-animal SPECT and SPECT/CT: application in cardiovascular research

Preclinical cardiovascular research using noninvasive radionuclide and hybrid imaging systems has been extensively developed in recent years. Single photon emission computed tomography (SPECT) is based on the molecular tracer principle and is an established tool in noninvasive imaging. SPECT uses gamma cameras and collimators to form projection data that are used to estimate (dynamic) 3-D tracer distributions in vivo. Recent developments in multipinhole collimation and advanced image reconstruction have led to sub-millimetre and sub-half-millimetre resolution SPECT in rats and mice, respectively. In this article we review applications of microSPECT in cardiovascular research in which information about the function and pathology of the myocardium, vessels and neurons is obtained. We give examples on how diagnostic tracers, new therapeutic interventions, pre- and postcardiovascular event prognosis, and functional and pathophysiological heart conditions can be explored by microSPECT, using small-animal models of cardiovascular disease

A prototype instrument for single pinhole small animal adaptive SPECT imaging

The authors have designed and constructed a small-animal adaptive SPECT imaging system as a prototype for quantifying the potential benefit of adaptive SPECT imaging over the traditional fixed geometry approach. The optical design of the system is based on filling the detector with the region of interest for each viewing angle, maximizing the sensitivity, and optimizing the resolution in the projection images. Additional feedback rules for determining the optimal geometry of the system can be easily added to the existing control software. Preliminary data have been taken of a phantom with a small, hot, offset lesion in a flat background in both adaptive and fixed geometry modes. Comparison of the predicted system behavior with the actual system behavior is presented, along with recommendations for system improvements

Conservation Management of Tasmanian Devils in the Context of an Emerging, Extinction-threatening Disease: Devil Facial Tumor Disease

An emerging infectious facial cancer threatens Tasmanian devils with extinction. The disease is likely to occur across the range of the devil within 5 years. This urgent time frame requires management options that can be implemented immediately: the establishment of insurance populations, in captivity, wild-living on islands, and aiming for eradication in areas that can be isolated. The long-term options of the spontaneous or assisted evolution of resistance or development of a field-deliverable vaccine are unlikely to be available in time. The disease's characteristic allograft transmission through intimate contact simplifies isolation of insurance populations and breaking transmission in suppression trials. Better knowledge of contact matrices in wild devils will help focus timing and demographic targets of removals. A metapopulation approach is needed that integrates captive and wild-living island and peninsula (disease suppression) populations to minimize the loss of genetic diversity over 50 years until either extinction and reintroduction can occur, resistance evolves or a field-deliverable vaccine is developed. Given the importance of the insurance populations and the low genetic diversity of devils, a conservative target for retention of 95% genetic diversity is recommended. Encouraging preliminary results of the first disease-suppression trial on a large peninsula show fewer late stage tumors and no apparent population decline. Limiting geographic spread or suppressing the disease on a broadscale are both unlikely to be feasible. Since the synergy of devil decline and impending fox establishment could have devastating consequences for Tasmanian wildlife, it is crucial to manage the dynamics of new and old predator species together