对PFU法中MacArthur-Wilson平衡模型的修改

考虑到环境压迫的因素,对PFU法中的MacArthur-Wilson平衡模型作了修改,推导出一个更为适用的新模型。小野外生态试验和室内毒理试验中提出4个功能参数(S_(eq),G,H,T_(90％))用于环境的生物监测。使用Monte Garlo序贯随机模拟算法和Marquardt算法估计模型参数并完成计算机程序的编制,最后还使用拟合差异度法检验实验模型。

安全ARP的Clark-Wilson模型化

ARP协议漏洞严重威胁着TCP／IP的安全，一些基于对称或非对称密钥机制的安全ARP协议被相继提出。本文介绍了ARP协议攻击的原理和几个最出名的基于对称或非对称密钥机制的安全ARP协议，引入Clark-wilson商业模型对ARP的完整性状态进行了分析，把改进协议Clark-Wilson模型化，在模型化的过程中找到了它们不能通过Clark-Wilson商业模型验证规则的关键点，并根据Clark-Wilson商业模型提出的经典场景，给出了相应的攻击场景。

基于Biba和Clark-Wilson策略的混合强制完整性模型

商业应用需要实施完整性策略保护.Biba模型提供了一种简洁的多级完整性控制方案,但是需要引入可信主体来保证实施的可用性.而Clark-Wilson模型通过可监控的状态转换提供了一种完备的完整性保护,但其复杂性影响了该模型的完整实现.提出的模型以Biba严格完整性策略为基础,同时根据可信主体在其生命周期所属的状态实施Biba低水标策略.对可信主体在其生命周期发生的状态转换及相应的低水标参数调整,采用Clark-Wilson模型来进行监控.在有效解决了Biba策略的可用性问题和Clark-Wilson模型监控量过大给系统带来的配置和运行负担问题的同时,继承它们的优点.证明了该策略融合方案是可行的、安全的.

Flexural fatigue behavior of injection-molded composites based on poly(phenylene ether ketone)

Flexural fatigue tests were conducted on injection-molded short fiber composites, carbon fiber/poly(phenylene ether ketone) (PEK-C) and glass fiber/PEK-C (with addition of polyphenylene sulfide for improving adhesion between matrix and fibers), using four-point bending at stress ratio of 0.1. The fatigue behavior of these materials was presented. By comparing the S-N curves and analyzing the fracture surfaces of the two materials, the similarity and difference of the failure mechanisms in the two materials were discussed. It is shown that the flexural fatigue failure of the studied materials is governed by their respective tensile properties. The matrix yielding is main failure mechanism at high stress, while at lower stress the fatigue properties appear fiber and interface dominated. (C) 1997 John Wiley & Sons, Inc.

Morphological, thermal, and mechanical properties of polypropylene/polycarbonate blend

This work deals with the effect of compatibilizer on the morphological, thermal, rheological, and mechanical properties of polypropylene/polycarbonate (PP/ PC) blends. The blends, containing between 0 to 30 vol % of polycarbonate and a compatibilizer, were prepared by means of a twin-screw extruder. The compatibilizer was produced by grafting glycidyl methacrylate (GMA) onto polypropylene in the molten state. Blend morphologies were controlled by adding PP-g-GMA as compatibilizer during melt processing, thus changing dispersion and interfacial adhesion of the polycarbonate phase. With PP-g-GMA, volume fractions increased from 2.5 to 20, and much finer dispersions of discrete polycarbonate phase with average domain sizes decreased from 35 to 3 mu m were obtained. The WAXD spectra showed that the crystal structure of neat PP was different from that in blends. The DSC results suggested that the degree of crystallization of PP in blends decreased as PC content and compatibilizer increased. The mechanical properties significantly changed after addition of PP-g-GMA. (C) 1997 John Wiley & Sons, Inc.

Ocean urea fertilization for carbon credits poses high ecological risks

The proposed plan for enrichment of the Sulu Sea, Philippines, a region of rich marine biodiversity, with thousands of tonnes of urea in order to stimulate algal blooms and sequester carbon is flawed for multiple reasons. Urea is preferentially used as a nitrogen source by some cyanobacteria and dinoflagellates, many of which are neutrally or positively buoyant. Biological pumps to the deep sea are classically leaky, and the inefficient burial of new biomass makes the estimation of a net loss of carbon from the atmosphere questionable at best. The potential for growth of toxic dinoflagellates is also high, as many grow well on urea and some even increase their toxicity when grown on urea. Many toxic dinoflagellates form cysts which can settle to the sediment and germinate in subsequent years, forming new blooms even without further fertilization. If large-scale blooms do occur, it is likely that they will contribute to hypoxia in the bottom waters upon decomposition. Lastly, urea production requires fossil fuel usage, further limiting the potential for net carbon sequestration. The environmental and economic impacts are potentially great and need to be rigorously assessed. (C) 2008 Elsevier Ltd. All rights reserved.

Geographic variation in the leaf essential oils of Juniperus sabina L. and J-sablina var. arenaria (E.H. Wilson) Farjon

The composition of the leaf oils from seven populations of J. sabina L., one population of Juniperus sabina var. arenaria (E. H. Wilson) Farjon were examined for their geographic variation. In addition, the leaf oils of J. chinensis L. and J. davurica Pall. were compared to J. sabina. Juniperus sabina var. arenarla, the sand loving juniper, oil was found to be very similar to that of J. davurica, Mongolia, and J. sabina, on sand dunes in Mongolia. This suggests that J. sabina var. arenaria might be conspecific with J. davurica. Farjon's move (2001) of J. sabina var. arenaria out of J. chinensis is supported. Considerable differentiation was found in populations of J. sabina from the Iberian peninsula. Cedrol, citronellol, safrole, trans-sabinyl acetate, terpinen-4-ol and beta-thujone were found to be polymorphic in several populations.