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We measured the stable carbon isotope ratios for muscle of the upland buzzards (Buteo hemilasius), plateau pika (Ochotoma curzoniae), root vole (Microtus oeconomus), plateau zokor (Myospalax fontanierii) and passerine bird species at the Haibei Alpine Meadow Ecosystem Research Station (HAMERS), and provided diet information of upland buzzards with the measurement of stable carbon isotopes in tissues of these consumers. The results showed that δ~(13)C values of small mammals and passerine bird species ranged from -25.57‰ to -25.78‰ (n = 12), and from -24.81‰ to -22.51% (n = 43), respectively, δ~(13)C values of the upland buzzards ranged from -22.60‰ to -23.10‰ when food was not available. The difference in δ~(13)C values (2.88‰±0.31‰) between upland buzzards and small mammals was much larger than the differences reported previously, 1‰-2‰, and showed significant difference, while 1.31‰±0.34‰ between upland buzzard and passerine bird species did not differ from the previously reported trophic fractionation difference of 1‰-2‰. Estimation of trophic position indicated that upland buzzards stand at trophic position 4.23, far from that of small mammals, i.e., upland buzzards scarcely captured small mammals as food at the duration of food shortage. According to isotope mass balance model, small mammals contributed 7.89% to 35.04% of carbon to the food source of the upland buzzards, while passerine bird species contributed 64.96% to 92.11%. Upland buzzards turned to passerine bird species as food during times of shortage of small mammals. δ~(13)C value, a useful indicator of diet, indicates that the upland buzzards feed mainly on passerine bird species rather than small mammals due to "you are what you eat" when small mammal preys are becoming scarce.

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青海省生态环境恶化的主要特征是 :草地退化 ,水土流失 ,土地沙化 ,冰川湿地退缩 ,自然灾害频繁 ,人畜饮水困难 ,农村能源短缺。当前生态环境治理面临着试验示范不够、缺少治理规划、种苗供应混乱、资金投入不够等问题 ,需要加强治理规划工作和技术支撑体系、建立生态环境治理责任制、紧密结合生产结构调整及草产业的发展等方面开展工作。需要依据草业科学的原理 ,在生态环境治理中重视生态工程设计的应用 ,对治理区按照草地农业系统四个生产层次统筹考虑优化生产结构 ,发挥各系统和层次间的耦合效应。生态环境治理面临的问题为草业科学原理的实践及发展提供了广阔的天地。

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虽然新的制造系统不断涌现 ,企业仍然对CIM给予很大广泛的认可。本文讨论了CIM设计中的一些关键问题。首先 ,根据业务过程重组来实施CIM至关重要 ,其次 ,必须采用CIM的功能体系结构规范和容纳各种功能系统 ,以便更好地执行业务流过程。同时 ,需要有相应的集成基础结构来支持整个企业的数据管理。

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可重构制造模式是一种指导管理和控制制造系统重构过程的制造哲理 ,它使制造系统有效地响应不断变化的环境。制造系统具有可重构能力是其生存和发展的基本手段 ,具有较高可重构性的公司在风云突变的环境中将远远超过其竞争对手。本文探讨了可重构制造模式的基本定义和内涵 ,并从组织、过程、产品、加工系统和信息平台等五个方面研究了制造系统的可重构性。

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供应链管理使企业在变化的市场环境中有效地与其它企业合作 ,取得集体竞争优势。本文首先讨论了后勤学与供应链管理的定义和之间的关系。本文认为供应链管理的核心是物流与信息流的控制。物流控制决策主要包括操作层次的库存补充和运输路径规划 ,以及战略层次的设施地点规划。信息流管理跨越部门与企业的界限将相关的应用集成起来。动态联盟协调各企业内部的生产经营活动 ,战略性地决定物流与信息流的构形。

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实验研究了pH对REE水/粒界面配分行为的影响: 氢氧化铁胶体对REE的作用在胶体形成开始以吸附为主, 然后是解吸, 最后是吸附/解吸趋向平衡; 轻稀土元素(LREE)和重稀土元素(HREE)的吸附率不同, 后者大于前者. 随pH增加, LREE和HREE在氢氧化铁胶体/水之间产生分异, 其配分系数比值(DLREE/DHREE)降低; DREE的分布模式呈现Y的异常(DY/DHo<1)并在低pH条件下呈现明显的四重效应. 实验结果证明自然界中存在REE四重效应. 除pH外, 地表水的化学类型以及离子强度也是控制REE四重效应以及微粒吸附态REE和溶解态REE之间产生分异的重要因素.

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This paper gives a brief review of R&D researches for light olefin synthesis directly and indirectly from synthesis gas in the Dalian Institute of Chemical Physics (DICP). The first pilot plant test was on methanol to olefin (MTO) reaction and was finished in 1993, which was based on ZSM-5-type catalyst and fixed bed reaction. In the meantime, a new indirect method designated as SDTO (syngas via dimethylether to olefin) was proposed. In this process, metal-acid bifunctional catalyst was applied for synthesis gas to dimethylether(DME) reaction, and modified SAPO-34 catalyst that was synthesized by a new low-cost method with optimal crystal size was used to convert DME to light olefin on a fluidized bed reactor. The pilot plant test on SDTO was performed and finished in 1995. Evaluation of the pilot plant data showed that 190-200 g of DME were yielded by single-pass for each standard cubic meter of synthesis gas. For the second reaction, 1.880 tons of DME or 2.615 tons of methanol produced 1 ton of light olefins, which constitutes of 0.533 ton of ethylene, 0.349 ton of propylene and 0.118 ton of butene. DICP also paid some attention on direct conversion of synthesis gas to light olefins. A semi-pilot plant test (catalyst 1.8 1) was finished in 1995 with a CO conversion > 70% and a C(2)(=)-C(4)(=) olefin selectivity 71-74% in 1000 h. (C) 2000 Published by Elsevier Science B.V. All rights reserved.