青冈栎林分空间结构对林下更新的影响

林分空间结构会显著影响其林下幼树更新。为明确其影响林下幼树更新的关键因子,以湖南省青羊湖国有林场青冈栎林天然次生林为研究对象,测量幼树株数密度、树高、地径和冠幅,计算混交度、大小比数、开敞度指数以及聚集指数代表林分空间结构,评价林下幼树更新情况,并用灰色关联度分析方法探究两者间的相关关系。结果表明,青羊湖国有林场13块青冈栎林样地林下更新幼树有6种,分属于4科5属,分别是青冈栎、苦槠、多脉青冈、南酸枣、黄檀、马尾松,青冈栎在更新幼树中占明显优势,是优势树种,幼树重要值为63.09%。青冈栎林各林分空间结构指数与林下更新指数均大于0.5,关联度较高,综合所有林分空间结构指数对林下更新指数关联度的均值来看,对林下更新的影响由大到小为大小比数>开敞度>聚集指数>混交度,大小比数对青冈栎林下更新影响最为显著。在促进青冈栎天然次生林林下更新时,应以调整林木大小分化程度为主,综合考虑林木空间分布格局的调整方案。     

Genome‐wide association analysis of salmon lice (Lepeophtheirus salmonis) resistance in a North American Atlantic salmon population

Our objective was to detect single nucleotide polymorphisms (SNPs) associated with resistance to the salmon louse in the Saint John River aquacultural population of North American Atlantic salmon using estimated breeding values (EBVs) and 6K genotypes from the parent‐generation and lice count phenotypes from the challenged, but ungenotyped, offspring‐generation. In 2011 and 2012, we challenged recent smolts with approximately 100 copepodids each. Fish were euthanized once the lice reached the chalimus stages and lice count, sex, tank and salt water weight were recorded. We used a multiple trait model to estimate breeding values for the parent‐generation using their own fresh water weights and the salt water weights and lice counts of the offspring‐generation. Salmon lice count heritability for untransformed and transformed data was 0.17 and 0.29 respectively. Two different genome‐wide association study methods were compared: (i) forward multiple linear regression and (ii) a mixed linear model using principal components to correct for population stratification as implemented in the egscore function of GenABEL. The two methods detected different SNPs located on different chromosomes. The multiple regression method incorporated 70 SNPs found on chromosomes 2, 7, 9, 12, 14, 15, 21, 22, 1p/23, 24. Many SNPs entered into the forward multiple regression are likely to be false positives from not correcting for the observed population stratification and cryptic relatedness. In contrast, the mixed linear model identified only two SNPs, one on chromosome 1p/23 (6.9%) and one on chromosome 1q (6.1%) consistent with louse‐resistance being a quantitative trait.     

优秀传统家训文化涵育大学生社会主义核心价值观探讨

家训文化是中华民族优秀的传统文化,其与社会、个人以及社会主义核心价值观的主流意识形态有着紧密的关联。高校在培育社会主义核心价值观的工作中,要做到细致、落实、落小,离不开优秀传统家训文化的熏陶。讨论了优秀传统家训契合社会主义核心价值观的价值诉求以及优秀传统家训文化在当前时代的价值,提出了优秀传统家训文化在高校培育社会主义核心价值观中的具体路径。     

贵州马铃薯田杂草群落调查

贵州是我国马铃薯主产区之一,然而尚未有当地马铃薯Solanum tuberosum田杂草发生情况的研究报道。我们在贵州省修文县、开阳县、息烽县、习水县、水城县等5个典型马铃薯种植区展开田间调查。在所调查的19块马铃薯田间共发现64种杂草,其中重要值位列前10的杂草依次为:粗毛牛膝菊Galinsogaquadriradiata、卷茎蓼Fallopia convolvulus、繁缕Stellaria media、尼泊尔蓼Polygonum nepalense、马唐Digitaria sanguinalis、酸模叶蓼Polygonum lapathifolium、藜Chenopodium album、野艾蒿Artemisia lavandulaefolia、凹头苋Amaranthus lividus、鸭跖草Commelina communis。平均每块样田中杂草种类数为12.05种,Shannon多样性指数平均值为9.88,Pielou均匀度指数平均值为0.87;样地两两之间的Jaccard差异性指数平均值为0.76,Bray-Curtis差异性指数的平均值为0.72。通过主成分分析对所调查的19块马铃薯田杂草群落进行分析,结果表明所调查的19块田可分为4个类群,类群1优势种为粗毛牛膝菊、卷茎蓼、马唐,类群2以马兰为单优势种,类群3以繁缕、看麦娘、猪殃殃、酸模叶蓼为优势种,类群4以粗毛牛膝菊、卷茎蓼、马唐、尼泊尔蓼为优势种。结论:贵州马铃薯田杂草群落的α和β多样性均较高,不同马铃薯种植地区杂草群落结构差异较大,一些具有贵州地区特色的杂草例如粗毛牛膝菊、尼泊尔蓼等在当地马铃薯田危害严重。     

茶红素分离及稳定性研究

采用茶汤有机试剂萃取分离,并分别经过反相C_(18)柱层析纯化,制备出乙酸乙酯层、正丁醇层和酸性正丁醇层三部分茶红素。根据紫外可见光波扫描计算出色价,并研究了茶红素在不同条件下的稳定性。结果表明,30%、50%和70%甲醇梯度洗脱,纯化后3类茶红素液相检测发现无咖啡碱和茶黄素,仅有少量儿茶素杂质。纯化后色素色价分别为乙酸乙酯层128.04,正丁醇层91.04,酸性正丁醇层76.16。遮光处理,p H=3酸性条件,45℃以下贮藏,有利于茶红素的稳定性。     

湿地红线的确定与管理

湿地红线是国家湿地保护法律法规的另一种体现形式，是湿地管理的手段和工具，也是进行湿地评价的尺度和标准。湿地红线的制定已到了关键时期，条件已经成熟，利用目前最新的湿地调查成果，从生态系统安全、社会文化和经济三个方面进行理论指导，科学地确定湿地的数值与空间红线；同时，为了让生态红线真正发挥作用，还需要制定相配套的法律法规，建立相应的考核机制、出台相关经济政策等作为保障。     

棉花芽黄材料主要光合特性和农艺性状的研究

以v1、v2、v3、v4、v5v6、v8、v9、v10、v11、v13、v14、v15、v16v17、v18、v19、vg和彭泽芽黄等17份芽黄突变体材料及中棉所58突变体中58vsp为研究对象,测定了各材料不同时期不同叶位的SPAD值、叶绿素荧光参数最大光化学效率值(Fv/Fm)和光系统Ⅱ量子产量(φPSⅡ),同时对各芽黄突变体材料的主要农艺性状和纤维品质性状进行了调查和研究。结果表明,芽黄材料作为一种叶色突变体,其叶片相对叶绿素含量在不同时期、不同叶位的差异较大,各芽黄材料均以倒5叶或倒4叶的SPAD值最高,刚展平的倒2叶的SPAD值最小,其中中58vsp的倒2叶SPAD值最低;随着植株的发育,所有芽黄材料在7月5日、15日其倒4、倒5叶的SPAD值达到最大。与光合作用密切相关的最大光化学效率值(Fv/Fm)和PSⅡ量子产量(φPSⅡ)在各芽黄突变体材料之间差异也较大,其中v2最高,v3、v19最低。另外还发现各芽黄突变体材料的主要农艺性状和纤维品质性状存在较大的差异。本文对于不同芽黄突变体材料特性的初步研究,将为更好地将芽黄突变体用于棉花遗传育种和分子生物学研究打下了理论基础。     

微波杀青对茶在制品物理特性影响的初探

以一芽一叶的福鼎大白茶鲜叶为原料,设定6个微波杀青的时间梯度(0、30、60、90、120、150 s),按时间点取样,测定在制品的含水率、容重、色差Lab值、长度、宽度等,研究微波杀青时间对茶在制品物理特性的影响。结果表明,随着微波杀青的进行,在制品的含水率在前90 s匀速缓慢下降,而后急速下降,容重在微波30 s后显著下降;茶在制品的平均相对长度差、相对宽度差和面积差呈现先降后升的趋势,在微波60~90 s时相对最小;在制品色差L值、|a|值、b值随着微波杀青的进行,呈先升后降的趋势,微波前90 s均较鲜叶有显著提升,而后显著下降。相关性分析表明,微波杀青时间和含水率均对L值、|a|值、b值、相对长度差等呈显著影响,总体上看以微波杀青60~90 s最有利于获得较优的外形属性。     

Appraisal and standardization of curvilinear velocity (VCL) cut‐off values for CASA analysis of Japanese quail (Coturnix japonica) sperm

One of the basic steps in objective analysis of sperm motility is the subdivision of a motile sperm population into slow, medium and rapid categories based on their velocity. However, for CASA analysis of quail sperm, the velocity values for categorization of slow, medium and rapid sperm have not yet been standardized. To identify the cut‐off values of “velocity curvilinear” (VCL) for quail sperm categorization, we captured and analysed 22,300 tracks of quail sperm using SCA^®‐CASA. The median and mean VCL values were 85 and 97 μm/s. To define the VCL cut‐off values, we used two methods. In the first, we identified the upper (rapid sperm) and lower (slow sperm) cut‐off values using: (i) median VCL ± 25% or ± 50% or ± 75% of median VCL value; (ii) first and third quartile values of VCL data (i.e. 25% cut‐off setting); and (iii) 33% and 66% of VCL data. Among these settings, sperm categories and their corresponding motility characteristics recorded using the “25%” setting (i.e. slow ≤36 ≤ medium ≤154 ≤ rapid) were found the most realistic and coherent with male ranking by fertility. In the second method, we calculated heteroscedasticity in the total VCL data using PCA and the two‐step clustering method. With this approach, the mean of the high and low clusters was 165 and 51 μm/s, respectively. Together, the mean from two methods suggested that, for SCA^®‐CASA categorization of quail sperm, sperm should be classed as “rapid” at VCL ≥160 μm/s and “slow” at VCL ≤45 μm/s.