浅析我国南方冬闲田种植一年生黑麦草的应用研究

针对我国南方地区冬闲田数量多、利用率低的现象,充分利用冬闲田种草养畜,不仅可以解决牲畜季节性青绿粗饲料缺乏问题,还能促进农民增收和农业可持续发展。一年生黑麦草由于适生范围广,鲜草产量高,营养丰富且柔嫩多汁,适口性好,家畜家禽喜欢采食,深受农户青睐,成为一种极具发展前途的越年生优质牧草,近年来在畜牧业生产中得到广泛应用。本文从一年生黑麦草生物性状、营养特性、冬闲田的丰产栽培技术、青贮技术以及在各类畜禽的饲喂研究角度进行综述,并指出今后的研究重点和方向。旨在为一年生黑麦草在畜牧业中的进一步推广应用提供参考。     

我国奶牛生产性能测定工作现状及发展趋势

本文介绍了我国开展奶牛生产性能测定工作的相关情况和取得的成效,分析了当前存在的主要问题,并对下一步发展提出了建议。     

两种光照下低海拔引种云锦杜鹃的光合作用日变化

以移栽的野生云锦杜鹃Rhododendron fortunei为材料,使用LI-6400便携式光合作用仪,分析10%光照和全光照下低海拔区域引种云锦杜鹃的光合日变化,结果显示10%光照下生长的云锦杜鹃蒸腾速率低于全光照下生长的云锦杜鹃,而水分利用效率高于全光照下云锦杜鹃的60.17%。两种光照下的云锦杜鹃净光合速率和蒸腾速率日变化呈现"单峰"型。全光照下净光合速率下降是非气孔限制引起的,而10%光照下则为气孔限制引起。研究说明种植在低海拔环境的云锦杜鹃喜光的特性并不因为温度高而改变,但夏季遮荫措施还是有必要的。     

江西引种无性系茶树良种的灰色关联度评价

[目的]为探究江西省引种省外无性系茶树良种的适应性与特征特性,从中筛选出适宜推广种植的茶树良种.[方法]以25份省外引进无性系茶树良种为材料,测定其农艺性状、化学成分含量、抗逆性和制茶品质等15项性状指标,采用因子分析性状指标的贡献度与相关性,最终利用灰色关联度法对引种品种进行综合分析和评价.[结果]15项性状指标的变异系数范围为5.08％～57.20％,其中13项在10％以上,表明所引进的无性系茶树良种在江西省的适应性差异性较大,其中生长势、EGC、耐旱性、耐旱性最大,发芽密度、一芽二叶百芽质量、一芽一叶期、总游离氨基酸、EC、ECG、EGCG次之,水浸出物和绿茶品质得分最小;因子分析提取的5个主因子能够解释引种品种适应性的79.19％的信息,各性状对主因子均有相应的贡献,性状指标中生长势、发芽密度、耐寒性和耐旱性之间相关性较大,水浸出物、茶多酚、EGCG、EGC和一芽二叶百芽质量之间相关性较大,EGC、EC、咖啡碱和一芽一叶期之间相关性较大;灰色关联度综合评价显示有11个品种的加权关联度在0.7以上,综合评价最好,依次为浙农117、福鼎大白茶、浙农113、鄂茶1号、迎霜、湘波绿2号、浙农902、白毫早、名山白毫、玉笋和春雨1号,这些品种的制茶品质优良,生长势较强、产量较大,物候期早,化学成分含量优异和抗逆性较强;11份品种评价为中等;3份评价较差.[结论]灰色关联度法可应用于茶树引种品种的适应性评价,综合评价最好的11份茶树良种可以在实际生产中进一步推广种植,也可以作为茶树品种选育时的遗传亲本材料,评价中等和较差的应谨慎引种.     

茄子株高性状鉴定与遗传分析

以长茄高代自交系125 和126 构建的茄子6 个不同世代的遗传群体〔P₁、P₂、F₁、F₂、 B₁（125×F₁）、B₂（126×F₁）〕 为试材，利用主基因+ 多基因混合数量性状遗传模型对茄子的株高性状进行多世代遗传联合分析。结果表明：供试亲本株高 性状差异显著，分离世代株高性状数值均呈单峰的偏正态分布，属于数量性状遗传。多世代遗传联合分析结果显示茄子株高 性状的最适遗传模型为C-0 模型，不存在主基因遗传效应，表现为多基因控制的加性- 显性- 上位性遗传模式。采用二阶 遗传参数进一步分析株高的多基因遗传效应，结果显示，茄子分离世代F₂、B₂ 的多基因遗传率分别为49.24%、22.77%，茄 子株高以多基因遗传为主。     

Construction and Partial Biological Characteristics Analysis of Listeriolysin S llsB Gene Deletion Strain

In order to analyze the effect of listeriolysin S (LLS) llsB gene deletion on the biological characteristics of Listeria monocytogenes (LM),this study used homologous recombination to construct the llsB gene deletion strain LM90-ΔllsB,and the biological characteristics of growth characteristics,median lethal dose (LD₅₀) and organ-borne bacteria were studied in healthy Kunming male mice at 8 weeks old and weighing 40 g±5 g.The llsB gene deletion strain was successfully constructed,and the deletion strain had good genetic stability through continuous passage to 20 generations in vitro.Based on its growth curve examination,we found that the growth rate of the mutant strain was slightly higher than that of the parent strain.The results of mice infection test showed that the LD₅₀ of the parent strain and the deletion strain were 10^6.17 and 10^6.50 CFU,respectively.Compared with the parent strain,the amount of bacteria load of the deletion strain in the liver and spleen of the mice was extremely significantly decreased (P<0.01),the results showed that the infection ability of the mutant strain on mice was obviously weakened.No Listeria monocytogenes was detected in the brain.The results suggested that llsB gene might have direct or indirect regulatory effect on some biological characteristics of LM90,and it would provide a theoretical basis for further understanding of the pathogenic mechanism of LLS,prevention and control of listeriosis.     

Nitrogen transformation mediated by nitrate-dependent iron oxidation in anoxic freshwater

Journal of Soils and Sediments - Fe(III) transformation to Fe(II) via the nitrate-dependent iron oxidation process, occurring in anoxic sediments, has an important role in the nitrogen cycle. In...     

生长后期干旱复水对饲草大麦产量、品质及叶绿素含量的影响

为研究水分胁迫对饲草大麦生长、产量、籽粒关键品质和相关生理指标的影响,于2017～2018年采用盆栽称重控水法对甘饲麦1号进行以干旱胁迫持续时间(T)为主因素(10、20、30 d)和旱后复水量为副因素(W1、W2和W3)的裂区试验,测定其株高、穗长、生育期、单株产量及构成因子、关键品质指标以及叶绿素含量的变化。结果显示:干旱胁迫时间显著影响了各项测定指标,各项测定指标均表现出随着干旱胁迫时间的延长其显著降低,指标测定值均表现出T1T2T3。较T1,T2和T3处理的株高显著降低了10.87和16.26 cm,生育期显著提前了5.12和14.00 d;穗粒数、千粒重和单株产量分别显著降低了37.77%和67.06%、15.68%和30.62%、28.72%和69.09%;籽粒蛋白质含量显著提高了4.33%和10.16%,籽粒淀粉含量显著降低了5.65%和22.78%,籽粒饱满度显著降低了12.83%和18.95%。在同一胁迫期内,除了籽粒蛋白质含量以外,其余各项测定指标值均随着复水量的减少而不同程度的降低,指标测定值均表现为W1W2W3,且在T2和T3胁迫期下较对照W1,W3降低尤为明显。通过测定饲草大麦叶片叶绿素含量发现:在T1和T2持续胁迫时间下,复水后W1和W2处理存在显著的补偿效应,而W3以及T3持续胁迫时间的所有复水处理均未产生显著的补偿效应。说明甘饲麦1号干旱复水补偿效应的利用应注意干旱胁迫持续时间不超过20 d(土壤最大持水量的60%～65%),旱后复水量不低于田间土壤最大持水量的55%～60%为宜。     

添加槐花粉对白三叶青贮发酵品质的影响

采用单因子随机设计，研究添加不同比例的槐(Sophora japonica)花粉对白三叶 (Trifolium repens)青贮发酵品质的影响，以期为槐花应用于青贮饲料生产提供科学依据。分别设置白三叶单独青贮(C)、95%白三叶 + 5%槐花粉青贮(T1)、90%白三叶 + 10%槐花粉青贮(T2)、85%白三叶 + 15%槐花粉青贮(T3)、80%白三叶 + 20%槐花粉青贮(T4)共5个处理。结果表明，白三叶单独青贮品质较差，添加槐花粉提高了青贮原料的干物质、水溶性碳水化合物含量和发酵系数，降低了缓冲能值，使得青贮后的感官评分、乳酸、乳酸 ? 乙酸、干物质、水溶性碳水化合物、粗蛋白质含量显著提高(P ≤ 0.05)，pH、氨氮 ? 总氮、乙酸、丁酸含量显著降低(P ≤ 0.05)。综合考虑，80%白三叶 + 20%槐花粉青贮能获得良好的青贮品质。     

27-Hydroxycholesterol modulates lung cancer cell proliferation by activation of LXR signaling pathway

AIM:To investigate the effect of cholesterol metabolite 27-hydroxycholesterol (27-OHC) on the proliferation of lung cancer cells. METHODS:Human lung cancer A549 cells were treated with 27-OHC at different concentrations (0, 0.3125, 0.625, 1.25, 2.5, 5 and 10 μmol/L) for 24~48 h. The cell viability, cell cycle, cell prolife-ration, the intracellular cholesterol levels and cholesterol metabolism-related molecule expression were subsequently assessed by CCK-8 assay, flow cytometry, EdU staining, tissue total cholesterol detection kit, real-time PCR and Western blot. RESULTS:27-OHC decreased the viability of the A549 cells in a dose-and time-dependent manner (P<0.01) and inhibited the cell proliferation (P<0.05). The expression of typical liver X receptor (LXR) downstream target proteins including ATP-binding cassette transporter A1 (ABCA1), low-density lipoprotein receptor (LDLR), and 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CR) were modulated, which promoted the efflux of intracellular cholesterol, and reduced cholesterol influx and de novo synthesis, resulting in decreased intracellular cholesterol levels and cell viability. Furthermore, the inhibitory effect of 27-OHC on A549 cell viability was significantly attenuated after the LXR pathway was partially blocked by 5 μmol/L GSK2033 treatment (P<0.05). CONCLUSION:27-OHC inhibits A549 cell prolife-ration via activation of LXR signaling pathway.