Lake Erie water quality has improved dramatically since the degraded conditions of the 1960s. Additional gains could be made,
but at the expense of further investment and reductions in fishery productivity. In facing such cross-jurisdictional issues,
natural resource managers in Canada and the United States must grapple with conflicting objectives and important uncertainties,
while considering the priorities of the public that live in the basin. The techniques and tools of decision analysis have
been used successfully to deal with such decision problems in a range of environmental settings, but infrequently in the Great
Lakes. The objective of this paper is to illustrate how such techniques might be brought to bear on an important, real decision
currently facing Lake Erie resource managers and stakeholders: the choice of new phosphorus loading targets for the lake.
The heart of our approach is a systematic elicitation of stakeholder preferences and an investigation of the degree to which
different phosphorus-loading policies might satisfy ecosystem objectives. Results show that there are potential benefits to
changing the historical policy of reducing phosphorus loads in Lake Erie. 相似文献
Humic substances play empirically several essential functions in biogeochemical cycles such as storage of carbon, pollutants, nutrients and water, yet the underlying mechanisms remain poorly known because their precise molecular structure is largely unknown so far. Here, we extracted humic substances from biomass waste of bell pepper, fennel, artichoke, coffee ground, coffee husks, and nursery residues. We analyzed humic extracts by ultra-high resolution Orbitrap Fusion Lumos Tribrid 1 M mass spectrometry, using both positive photoionization and negative electrospray ionization modes, and by 13C cross polarization/magic angle spinning nuclear magnetic resonance spectroscopy. We identified 5000–7000 unique organic compounds in humic substances by integrating photoionization with electrospray ionization. The chemical distribution of all components was depicted by nuclear magnetic resonance. Humic substances from green composts are composed by a wide variety of hydrophilic and hydrophobic moieties, thus providing the required biosurfactant properties for effective soil washing capacities, with carboxyl-rich alicyclic molecules, fatty acids, and phenolic acids as major constituents. Overall, our findings provide a major insight in the molecular structure of humic substances, thus opening research on mechanisms ruling the origin, fate and behavior of humic substances.
A study on variable charge soils (volcanic Italian and podzolic Scottish soils) was performed to investigate the influence of soil
properties on the chemical composition of soil solution. Zinc speciation, bioavailability and toxicity in the soil solution were examined.
The soils were spiked with increasing amounts of Zn (0, 100, 200, 400 and 1000 mg/kg) and the soil solutions were extracted using
rhizon soil moisture samplers. The pH, total organic carbon (TOC), base cations, anions, total Zn and free Zn2+ in soil solution were
analysed. A rapid bioassay with the luminescent bacterium Escherichia coli HB101 pUCD607 was performed to assess Zn toxicity.
The influence of soil type and Zn treatments on the chemical composition of soil solution and on Zn toxicity was considered and
discussed. Di erent trends of total and free Zn concentrations, base cations desorption and luminescence of E. coli HB101 pUCD607
were observed. The soil solution extracted from the volcanic soils had very low total and free Zn concentrations and showed specific
Zn2+/Ca2+ exchange. The soil solution from the podzolic soil had much higher total and free Zn concentrations and showed no evidence
of specific Zn2+/Ca2+ exchange. In comparison with the subalkaline volcanic soils, the acidic podzol showed enhanced levels of toxic
free Zn2+ and consequently stronger effects on E. coli viability. 相似文献
The conventional (hot pressing or HP) and the novel (spark plasma sintering or SPS) consolidation techniques were compared when processing Ti–Al2O3–TiC powders obtained by self-propagating high-temperature synthesis (SHS). It was found that the two different methods are able to produce similar materials, in some cases (Vickers hardness and wear rate) slightly better for SPSed samples. However, SPS does not need sintering temperatures as high as HP to obtain fully dense products. Most significantly, processing times were strongly reduced when adopting the SPS technique instead of HP, i.e. 4–7 min and about 5 h, respectively. Finally, when the total energies required during each SPS or HP experiment were compared, it was found that the use of the SPS technology allowed for an energy saving in the order of 90–95%. This fact makes SPS significantly advantageous from environmental and economical points of view compared to HP. 相似文献