35技术在城市森林研究中的应用

总结国内外3s技术在城市森林研究领域应用现状，分析其不足，即遥感学家与植物生态学家缺乏沟通、被动遥感优势尚未挖掘、生态系统服务制图滞后、生态系统管理中忽视信息系统建设，以及景观规划的精确性与客观性有待提高等，在此基础上提出相应改进建议，以期为我国城市森林的3S技术应用和城市森林建设工作提供借鉴。     

大豆油分含量SSR标记及QTL定位

大豆油分含量是数量遗传性状。为了选育高油品种,有效利用高油基因和转基因研究,并使其广泛应用于育种和生产实践,通过构建群体,利用分子标记手段对油分基因在基因图谱上的位置进行了标记,结果表明,标记Satt491和油分含量相关,定位于E连锁群上。     

平菇培养料发酵过程理化因素及微生物变化研究

通过对平菇(Pleurotus ostreatus)玉米芯培养料进行发酵处理,监测玉米芯发酵料的堆温和pH值变化,对不同发酵阶段进行微生物区系分析并测定了发酵过程中脱氢酶和碱性磷酸酶的变化。结果表明,在玉米芯培养料的发酵过程中,堆温先升高后降低,而pH值先降低后升高。微生物主要以细菌和放线菌为主,真菌数量很少。随着发酵的进行,细菌和放线菌数量,脱氢酶以及碱性磷酸酶的活性呈逐渐上升趋势。     

一种改进的树冠截留降雨试验方法

设计了一种基于计算承雨器四周各1m范围内树冠郁闭度，进而通过一次降雨试验可观测到不同郁闭度级林冠截留降雨量的方法，解决了以往林冠截留降雨量测试中林冠疏密和树冠间隙分布不均引起的测量结果误差较大的难题。     

陆地棉对黄萎病抗性的分子标记研究

 利用陆地棉标准系TM-1和常抗棉2个陆地棉品种杂交并自交,获得109个F₂单株及F_2:3家系为作图群体,以SSR、RAPD和SRAP 3种分子标记进行抗黄萎病性状的分子标记筛选。结果从1611对(条)引物中仅筛选到70对(条)多态性引物,获得75个多态性位点并进行标记间的连锁性分析。75个标记构建了一个包括15个连锁群,全长535 cM的陆地棉品种间分子标记遗传连锁图,标记间平均距离为11.15 cM,有27个标记不能进入任何连锁群。连锁群的标记数最少2个,最多6个;长度从1.0 cM到92.7 cM不等。对其F_2:3家系的成株期抗黄萎病性状即平均病情指数的分布进行分析,显示其呈正态分布,进一步说明陆地棉对黄萎病的抗性为数量遗传;单标记分析及复合区间作图,检测出与抗黄萎病性相关的3个QTL,分别位于第3、5、6连锁群上,贡献率分别为14.15%、3.45%和18.78%。另外,对该群体生长过程中黄萎病不同发病高峰期的病情也进行了分析。     

Evaluation and mapping of soil erosion susceptibility: an example from Kenya

Abstract. The erosion susceptibility of the Erosion Research Farm at Kabete Campus was mapped using a qualitative parametric method. A grid soil survey of the 4 ha farm was combined with a map of slope gradients, slope segments being delineated by breaks in slope. Rainfall erosivity and soil erodibility were also measured. Areas with the greatest erosion susceptibility according to this method were those occupying convex slope positions and slopes of more than 30%. Field observations and soil loss measurements generally supported the erosion susceptibility rating map produced by this method. The soil and erosion susceptibility maps were useful for planning erosion control measures and for selecting suitable sites for runoff plot experiments.     

玉米雄性不育突变体mi-ms-3的遗传分析及分子鉴定

Maize is one of the best crops in the utilization of heterosis. Male sterile lines are important germplasms for the hybrids production. A male sterile mutant named mi-ms-3 was obtained by screening in a mutator insertion library. The number of male anthers in tassel decreased and not exserted. There were few anthers with only two pollen sacs in the mutant tassels, and some of the anthers were degenerated to membranous and formed filaments at their ends. Although pollens in the anthers could be stained by I₂-KI, pollen shedding was abnormal and the number of pollen grains decreased. The number of silks in the ear of the mutant increased, and there was a sterile grain on both sides of the maturated kernel. Fertility of F₁ plants, which were obtained by hybridization between mi-ms-3 and maize inbred Mo17, was normal. Genetic analysis of F₂ population showed that the mutant phenotype was controlled by a recessive gene. The candidate gene was preliminarily mapped on the long arm of chromosome 3 by BSA and it was located between a SSR marker and an Indel marker with a distance of 1.5 cM. There are 21 candidate genes in this region. It was finally found that the insertion mutation of Mu transposon occurred at 30 bp upstream of the coding region of zm00001d042618 (zmm16) by transponson tagging and sequencing analysis. The results showed that mi-ms-3 was a new allele of sts1, which caused by a single base mutation in the coding region. RT-PCR analysis indicated that the expression of zmm16 in the mutant was decreased. The identification of the new allelic mutant of sts1 in this study would provide new materials for the study of flower development and hybrid seed production.     

Scale dependence of tree abundance and richness in a tropical rain forest,Malaysia

Abundance and richness are the two fundamental components of speciesdiversity. They represent two distinct types of variables of which the formerisadditive when aggregated across scales while the latter is nonadditive. Thisstudy investigated the changes in the spatial patterns of abundance andrichnessof tree species across multiple scales in a tropical rain forest of Malaysiaandtheir variations in different regions of the study area. The results showedthatfrom fine to coarse scales abundance had a gradual and systematic change inpattern, whereas the change in richness was much less predictable and ahotspot in richness at one scale may become acoldspot at another. The study also demonstrated that differentmeasures of diversity variation (e.g., variance and coefficient of variation)can result in different or even contradictory results which further complicatedthe interpretation of diversity patterns. Because of scale effect the commonlyused measure of species diversity in terms of unit area (e.g.,species/m²) is misleading and of little use in comparing speciesdiversitybetween different ecosystems. Extra care must be taken if management andconservation of species diversity have to be based on information gathered at asingle scale.This revised version was published online in May 2005 with corrections to the Cover Date.     

Analysis of FMO genes and off flavour in pork

Off flavours in pork sometimes produce tastes such as sourness, fishy, metallic or other non‐typical flavours and are often caused by low pH. Loss of function mutations in flavin containing mono‐oxygenase 3 (FMO3) are known to be associated with a fishy off flavour in both chicken eggs and cow's milk and a similar autosomal recessive disorder is present in humans resulting in a fishy odour. FMO3 is a member of a gene family that is clustered on human chromosome 1. Comparative mapping suggested that FMO3 and the remaining FMO genes (ex. FMO1 and FMO5) might map to the orthologous region on pig chromosome 9 (SSC9) where a quantitative trait locus (QTL) for off flavour was previously identified. Primers were designed to amplify FMO1, FMO3 and FMO5 gene fragments and several SNPs were discovered and genotyping tests developed. The genotypes from the Iowa State University Berkshire × Yorkshire resource population were used to linkage map FMO1 and FMO3 to SSC9 and FMO5 to pig chromosome 4 (SSC4). QTL and associations analyses were performed using the map containing FMO1 and FMO3. Results demonstrated that FMO3 and FMO1 mapped less than 1 cM away from the peak for the off flavour QTL previously detected on SSC9 and provide indications of an association between the FMO3 polymorphism and off flavour in pork.     

畜禽数量性状基因座位的精细定位

数量性状基因座位(QTL)的精细定位是实施QTL克隆及标记辅助选择(MAS)的重要基础。然而就目前畜禽QTL定位的结果来看,除了通过候选基因法识别的少数基因外,大多数QTL定位的精度仍无法满足实际应用的要求。为进一步提高QTL定位的精度,缩小QTL定位的置信区间,人们相继提出并发展了一系列新的QTL定位方法。本文在分析畜禽QTL定位的基本方法及影响畜禽QTL定位精度的主要因素基础上,对提高QTL定位精确性的策略和方法进行了相应的探讨。