壳聚糖对大豆蛋白发酵液的絮凝研究

对用壳聚糖絮凝大豆蛋白发酵液进行研究,讨论pH值、絮凝剂浓度、温度和搅拌时间对絮凝效果的影响,结果是壳聚糖用量200 mg/L、pH值为4、搅拌12 min、温度30℃时效果最好.     

基于MaxEnt模型的毛红椿适生区预测

[目的]了解环境因子对毛红椿适生区分布的影响,为其资源保护、引种及其人工林的发展提供参考。[方法]基于MaxEnt模型能利用现存不完整、小样本、离散型分布数据构建物种适生区预测模型,用受试者工作曲线线下面积(AUC)检验预测模型的精度,面积越大精度越高等优点,本研究应用毛红椿在云南的分布数据及1个地型因子和6个气候因子,来构建其适生区分布模型。[结果]毛红椿适生区分布MaxEnt模型平均训练AUC和平均测试AUC分别为0.891、0.885,说明对毛红椿适生区的预测是可靠的;降水量变异系数和最干季度降水量是决定毛红椿适生区分布的主要因子,年均气温变化范围、最冷季度平均气温、最湿季度降水量、最冷季度降水量是次要因子。在当代和未来(2050S、2070S)气候变暖条件下(RCP2.6情景),云南省和全国适生区面积计算结果直观、定量的反应了全球变暖对毛红椿适生区变迁的影响。[结论]预测云南省及全国的毛红椿适生区随全球变暖而小幅萎缩。     

干燥介质相对湿度对胡萝卜片热风干燥特性的影响

为了探究相对湿度和阶段降湿对热风干燥过程的影响,该文在干燥温度60℃、风速3.0 m/s条件下,研究了相对湿度(20%、30%、40%、50%)及第一阶段相对湿度50%保持不同时间(10、30、60、90 min),第二阶段相对湿度20%下,胡萝卜片的干燥特性和温度变化规律;利用Weibull分布函数对干燥曲线进行拟合并分析干燥过程,结合尺度参数估算水分有效扩散系数;基于复水比、色泽、干燥时间和能耗对不同相对湿度条件下的干燥过程进行评价。研究结果表明:相对湿度保持恒定条件下,干燥速率先上升后下降,且相对湿度越低干燥速率越大。降低相对湿度有利于缩短干燥时间,热风相对湿度20%比50%条件下干燥时间缩短了27.6%;分段降湿干燥条件下,热风相对湿度50%保持30min后降低为20%,其干燥时间比相对湿度恒定为20%条件下缩短了18.5%,干燥过程出现2个升速阶段;Weibull分布函数可以很好地描述胡萝卜恒定湿度和阶段降湿干燥过程。尺度参数α范围在1.864~3.635 h之间,形状参数β值在1.296~1.713之间,水分有效扩散系数在1.17×10-9~2.92×10-9 m2/s之间。对绿红值、复水率、能耗和干燥时间进行综合评价显示,热风相对湿度50%保持30 min干燥条件下绿红值最高为41.4,能耗相比于恒定相对湿度20%条件下减少了6.0%,复水比较高为3.81,综合评分较高为0.91。该文揭示了干燥介质相对湿度对胡萝卜片干燥特性的影响规律,对于优化干燥介质湿度控制策略以提高干燥速率和品质,降低干燥能耗提供了科学依据和技术支持。     

新疆棉田牧草盲蝽的空间分布规律

为明确新疆棉田牧草盲蝽Lygus pratensis(Linnaeus)的空间分布型,于2012-2014年对新疆喀什地区棉田牧草盲蝽种群数量进行了系统调查,应用5种聚集度指数、Iwao m*-m回归方程和Taylor幂法则分析判定牧草盲蝽成虫、若虫及整个种群(成虫和若虫)在棉田的空间分布型,并利用种群聚集均数分析聚集原因。结果表明,牧草盲蝽成虫、若虫及整个种群的久野指数C_A0、负二项分布参数k0、丛生指数I0、聚块指数m*/~-1,表明三者在新疆棉田均呈聚集分布。且牧草盲蝽成虫和若虫的Blackith聚集均数λ2,说明二者在棉田的聚集是由环境因素引起的。Iwao m*-m回归分析结果表明,牧草盲蝽成虫、若虫和整个种群个体间相互吸引,分布的基本成分为个体群(α0、β1);Taylor幂法则分析结果表明,牧草盲蝽成虫、若虫和整个种群在棉田更趋向于聚集分布,聚集度依赖于密度。     

十字花科蔬菜害虫生物防治研究进展

十字花科蔬菜主要害虫有菜青虫、小菜蛾、甜菜夜蛾、猿叶虫等,其中有些害虫抗药性的迅速增加导致频繁暴发,因此生物防治对于防治十字花科蔬菜害虫是至关重要的。本文综述了国内外目前对十字花科蔬菜害虫天敌昆虫、病原微生物的调查研究进展,并探讨对植物提取物和昆虫生长调节刑等的利用现状。     

Genetic parameters for spawning and growth traits in the Pacific white shrimp (Penaeus (Litopenaeus) vannamei)

The aim of this study was to estimate genetic parameters for spawning traits and growth traits in a breeding line of Pacific white shrimp, Penaeus (Litopenaeus) vannamei, selected for growth and survival. Traits studied were number of eggs (NE) and number of nauplii (NN) and female body weight at insemination (FWI) and body weight at 130 days of age (BW130). Genetic parameters were estimated using a multivariate animal model. Heritability for NE and NN were estimated as 0.13 ± 0.04 and 0.03 ± 0.04 respectively. The contribution to NN total variation due to ‘factors associated with male’ effect was estimated as 0.47 ± 0.07. In the cases of FWI and BW130, heritability was estimated as 0.44 ± 0.08 and 0.19 ± 0.03 respectively. Genetic correlation between FWI and NE was estimated as 0.49 ± 0.15, between FWI and NN as 0.54 ± 0.39 and between NE and NN as 0.27 ± 0.41, whereas the genetic correlations of FWI, NE and NN with BW130 were 0.30 ± 0.13, ?0.21 ± 0.19 and ?0.25 ± 0.38 respectively. Although it is important to perform more studies on this issue, our results found no evidence of a genetic antagonistic effect between female reproductive traits and body weight at harvesting (130 days of age) in P. vannamei.     

Polymorphism of <Emphasis Type="Italic">Got2</Emphasis> DNA sequences sheds light on <Emphasis Type="Italic">Aegilops tauschii</Emphasis> Coss. intraspecies divergence and origin of <Emphasis Type="Italic">Triticum aestivum</Emphasis> L.

DNA sequences of nuclear gene Got2 was studied in 60 accessions of Aegilops tauschii, 29 of subsp. tauschii and 31 of subsp. strangulata. It was found that Got2 allozyme polymorphism in Ae. tauschii is due to a single, unique, mutation which led to replacement of glutamic acid by isoleucine in residue 256 of the enzyme molecule, encoded by Got2. As revealed by Got2 DNA sequences variation, initially in its history Ae. tauschii was presented by subsp. strangulata, and among phylogenetic lineages of subsp. strangulata, the lineage “t-9¹s” (TauL3) is the most ancient, a relict one. Subspecies tauschii is relatively “young”. Initially it was presented by the lineage marked by combination of allozyme alleles Got2 ¹⁰⁵ and Acph1 ¹⁰⁰. In the past it inhabited the Continental area from Caucasia to Pakistan, but later on it was forced out by newly originated, now—a major lineage of subsp. tauschii, marked by Got2 ¹⁰⁰. This lineage extended the Continental area of the species up to Kirgizstan, but actually failed to penetrate into pre-Caspian area, occupied by subsp. strangulata. These results essentially differ from those obtained previously, using chloroplast DNA (cpDNA) sequences polymorphism. As revealed by cpDNA, the major, “usual”, subsp. strangulata (TauL2) is “younger” than subsp. tauschii, which resided on phylogenetic tree between relict lineage “t-9¹s”of subsp. strangulata—and major subsp. strangulata. But both cpDNA and Got2 DNA sequences indicate that the level of genetic variation in subsp. tauschii is much lower than in subsp. strangulata. According to Got2 DNA sequences variation, it was Ae. tauschii subsp. strangulata lineage “k-109″ which donated genome D to Triticum aestivum L. This lineage includes accessions: k-109 from South-Eastern Precaspian Azerbaijan; KU-2105, KU-2159 from Western Precaspian Iran; KU-2080 from Eastern Precaspian Iran.     

高山杜鹃成都平原越夏生长研究

为加强对高山杜鹃的引种栽培,筛选出适合成都平原栽植的高山杜鹃品种,对引进的11个品种高山杜鹃的整株生长指标（冠幅、株高、地径、分蘖能力）、枝条生长指标（分枝数、最长分枝长度、单枝粗度、最长枝叶片数）、叶片生长指标（叶长、叶宽、叶片厚度）、夏稍长度以及热害指数进行评估。结果表明,引进的11个品种高山杜鹃均能在一定程度上适应成都平原越夏生长,其中‘王妃’的综合表现最好,尤其是其冠幅、株高、地径、最长分枝长度、单枝粗度、叶长、叶宽,在引种2个月后的增幅分别达到了131.43%、155.07%、53.79%、103.65%、26.66%、21.51%、27.34%;‘喜悦’的热害指数最低,几乎不受害。此外,‘粉蜜’、‘红溢’也表现不俗。因此,引进高山杜鹃品种‘王妃’、‘粉蜜’、‘红溢’、‘喜悦’适应成都平原的越夏生长,可进一步推广栽植。     

液相芯片技术同时检测六种猪繁殖障碍病毒的方法研究

在GenBank中收集猪细小病毒(PPV)结构蛋白VP2基因、猪圆环病毒2型(PCV2)的ORF2序列、猪伪狂犬病毒(PRV)的gB基因、猪繁殖与呼吸综合征病毒(PRRSV)的NSP2基因、猪瘟病毒(CSFV)的E2基因和乙型脑炎病毒(JEV)的M基因,利用Primer5.0等分子生物学软件对收集的序列分析比较,筛选出上述基因的特异保守序列并设计引物和探针,将设计好的探针与相应的微球偶联,优化条件,建立检测方法。结果表明:建立的检测PPV、PCV2、PRV、PRRSV、CSFV、JEV6种病毒核酸的多重液相芯片技术具有较好的特异性、敏感性和稳定性,对PPV、PCV2、PRV、PRRSV、CSFV、JEV6种病毒核酸的最低检出量分别为8.50×10~2copies/μL、2.87×10~2copies/μL、2.07×10~2copies/μL、2.61×10~2copies/μL、2.34×10~2copies/μL、2.05×10~2copies/μL,与相应病毒PCR/RT-PCR检测方法相比,敏感性提高了100~1000倍;对临床388份样品同步进行荧光PCR与液相芯片检测,结果99.87%相符。本方法为液相芯片技术在动物多病毒快速高通量检测、鉴别诊断等应用方面奠定了基础。