Melanin-based colorations signal strategies to cope with poor and rich environments

One hypothesis for the maintenance of genetic variation states that alternative genotypes are adapted to different environmental conditions (i.e., genotype-by-environment interaction G×E) that vary in space and time. Although G×E has been demonstrated for morphological traits, little evidence has been given whether these G×E are associated with traits used as signal in mate choice. In three wild bird species, we investigated whether the degree of melanin-based coloration, a heritable trait, covaries with nestling growth rate in rich and poor environments. Variation in the degree of reddish-brown phaeomelanism is pronounced in the barn owl (Tyto alba) and tawny owl (Strix aluco), and variation in black eumelanism in the barn owl and Alpine swift (Apus melba). Melanin-based coloration has been shown to be a criterion in mate choice in the barn owl. We cross-fostered hatchlings to test whether nestlings sired by parents displaying melanin-based colorations to different extent exhibit alternative growth trajectories when raised by foster parents in poor (experimentally enlarged broods) and rich (experimentally reduced broods) environments. With respect to phaeomelanism, barn owl and tawny owl offspring sired by redder parents grew more rapidly in body mass only in experimentally reduced broods. With respect to eumelanism, Alpine swift offspring of darker fathers grew their wings more rapidly only in experimentally enlarged broods, a difference that was not detected in reduced broods. These interactions between parental melanism and offspring growth rate indicate that individuals display substantial plasticity in response to the rearing environment which is associated with the degree of melanism: at least with respect to nestling growth, phaeomelanic and eumelanic individuals are best adapted to rich and poor environments, respectively. It now remains to be investigated why eumelanism and phaeomelanism have a different signaling function and what the lifelong consequences of these melanism-dependent allocation strategies are. This is important to fully appraise the role played by environmental heterogeneity in maintaining variation in the degree of melanin-based coloration.     

关于城乡生态经济一体化规划原则的思考

依据城乡生态环境中存在的一系列问题，提出应将生态经济观念引入社会经济发展中去，用生态学观点指导社会经济活动，对自然资源进行合理的开发利用；充分利用环境容量，发展环保产业，开发绿色产品。同时，由于城乡是一个完整的体系，只有进行城乡生态经济一体化规划，才能保证生态的良性循环。规划要考虑到：①打破行政区划，疏通物流渠道。②建设绿地中的城市，确保城市中的绿地。③有秩序分步骤发展生态经济。④为全球环境保护作     

退耕还林工程对黄土高原土地利用/覆被变化的影响——以陕西省安塞县为例

退耕还林工程(Sloping land conversion program, SLCP)可快速改变土地利用/覆被格局。论文以黄土高原典型沟壑区--陕西省安塞县为例,利用MSS/TM/ETM+卫星遥感影像,获取研究区6个时期土地利用/覆被的时空信息,通过统计模型,定量分析了研究区SLCP对土地利用/覆被格局的影响。草地、耕地及林地为研究区三大主要土地利用/覆被类型,研究区土地利用/覆被变化整体处于不平衡态势;整个研究时段内,耕地先增后减,整体减少38.4%;林地先减后增,整体增加4.36%;灌木林地和草地减少,而未成林造林地快速增加;SLCP显著加强了耕地的递减趋势,并大幅增加了未成林造林地面积,至2010年未成林造林地面积显著大于天然林地的面积。这些变化可能具有降低土壤侵蚀与产流量、改善土壤结构、增加土壤碳吸收等效应;SLCP能提高农民收入,且大部分农民支持SLCP;但其负面效应亦不可忽视。研究将有助于对SLCP效应的全面理解,并可为该区生态恢复工程的规划与决策及生态环境保护提供参考。     

本溪市空气质量控制方案实施评估

利用攻坚计划行动方案所涉及的污染源排放清单和扩散模型计算了环境中的污染物浓度，并将污染物浓度／人口分布和剂量一反应函数联系起来，根据方案实施前后污染物排放量的变化，分析对人体健康影响的变化，将损害的减少程度进行货币化计算，继而将影响成本和削减方案成本进行比较，评估方案的效益。     

遗传和模拟退火算法在水质模型参数确定中的应用简介

水质模型参数的确定是构建水质模型的基础。相对于传统优化方法,现代优化算法的优势日趋明显。本文在基于现代优化算法的水质模型参数确定研究背景下,介绍了具有代表性的遗传算法和模拟退火算法,并对该两种算法的应用现状进行综述,旨在推进该领域的进一步探索。     

都江堰市红色村干沟泥石流活动特征及危险性评估

"5·12"四川汶川大地震导致灾区地质灾害危险性大大增强,严重影响了周边居民的生命财产安全。都江堰市虹口乡红色干沟泥石流灾害隐患点是其中之一。根据泥石流的成因、类型、规模,以及泥石流的活动特征,对泥石流活动进行了危险性评估,指出泥石流防治工程方案应采用以排为主,适当拦挡的原则,建拦挡坝用以消能、调节泥石流流量;建防护堤用以限制泥石流漫流,对居民区进行有效防护。     

基于遗传算法的前馈神经网络火灾探测

分析了前馈神经网络火灾探测的基本原理;针对ＢＰ算法的缺陷,提出用遗传算法（ＧＡ）和ＢＰ相结合的一种方法,即：ＢＰ－ＧＡ算法;并把ＢＰ－ＧＡ算法用于火灾探测的模拟,结果表明：前馈神经网络是处理火灾信号的良好方法,ＢＰ－ＧＡ算法提高了网络的收剑性。     

1991年世界地震灾情及地震活动特征

为适应“国际减灾十年活动”的需要,系统整理了1991年世界地震灾情及重要地震。统计结果表明:全世界1991年全年因地震死亡人数为2084人,中国只有一人;受伤人数约6500人,中国将近700人;倒塌房屋约62万间。全年直接经济损失粗略估算,国外2.7～3.2亿美元,国内约3.3亿人民币。对1991年度地震活动特点进行了简要分析。     

下扬子地区分区走时表及计算机查表实用程序的编制

一般地震走时表是由一定间隔震中距查算各震相走时。本文所介绍的根据P与S波走时差值由计算机实时快速编制和查算区域地震走时表的方法和程序,适用于震源在壳内任意深度,可含低速层的水平均匀分层模型。此外,本文还给出了下扬子三个分区、三种深度的走时表,以供没有计算机的台站或地震现场作精细定位之用。     

Usefulness of linkage disequilibrium of KM-19 and XV-2c DNA probes for genetic counselling in a high-risk cf family

A French couple with an individual risk of carrying the cystic fibrosis (CF) mutation of 1/2 sought genetic counselling. From the DNA haplotypes generated by XV-2c and KM-19 RFLPs, it could be deduced that only one subject was a carrier, lowering the risk of having a CF baby from 1/16 to 1/200. The strong linkage disequilibrium between these RFLPs and the CF allele observed in France reduced the risk to 1/1600.