ST贴壁细胞悬浮驯化及应用

为将ST贴壁细胞通过自主驯化,使其能在ST-S细胞无血清培养基中悬浮生长且能稳定传代,在摇瓶中实现高密度生长,并应用于猪伪狂犬病毒(PRV)悬浮培养,经ST-A低血清培养基适应培养,对一株贴壁的ST细胞进行了无血清的全悬浮驯化,并将PRV在悬浮细胞中连续盲传培养。结果显示:ST悬浮细胞能在无血清培养基中传代,培养48 h至第3代后,所能达到的最终细胞密度为3.00×10^(6 )cells/mL以上;PRV连续培养至第5代,毒价可达到109.0 TCID50/mL。结果表明,用专用培养基可使ST贴壁细胞实现悬浮驯化,并可应用于PRV悬浮培养。本研究为获得高密度ST悬浮细胞和提高PRV增殖效率奠定了技术基础。     

基于PIV技术的圆形循环水养殖池流场

为研究进水管的设置距离和角度对双管进水式圆形循环水养殖池水动力特性的影响,该研究通过模型试验的方法,利用粒子图像测速技术（Particle Image Velocimetry,PIV）测量了不同进水管设置方式下养殖池内的流场。试验设计了3组进水管距池壁距离（进水管与池壁的最近距离,即进水管设置距离d）,每组距离工况下设计了8组进水角度（出水方向与养殖池切线形成的锐角,即进水管设置角度α）。利用PIV技术测量了不同工况下距离池底1 cm水层的流场,从水动力特征量（平均流速vavg和速度均匀系数U）分析进水管设置方式对养殖池水动力特性的影响。试验结果表明进水管设置方式明显影响养殖池的水动力特性：d=0时,随着α的增加,平均流速整体呈现先增大后下降的规律,在α=45°时取得最大值,但流场均匀系数随角度的增加而逐渐增加;d=1/4 r（r为养殖池半径）时,随着α的增加,平均流速和流场均匀系数都先缓慢增加然后再下降,分别在α=40°和30°时取得最大值;d=1/2 r时,随着α的增加,平均流速和流场均匀系数整体都呈现逐渐下降的趋势。综合比较24个试验工况的平均流速vavg和速度均匀系数U,建议将进水管设置为d=1/4 r,α=30°～40°,以期使养殖池内水动力特征有利于固体颗粒物的运动汇集,提升养殖池的集排污能力。该文研究成果可以为工厂化循环水圆形养殖池进水管设置方式提供参考。     

铅镉胁迫下马齿苋的种子萌发和幼苗生理响应

以马齿苋为试验材料,通过水培法研究马齿苋在铅、镉单一胁迫下种子萌发及幼苗生理指标的影响。结果表明：低浓度的铅胁迫对马齿苋种子萌发影响不大,但高浓度则显著抑制其种子萌发,2 000 mg/L铅处理下失去萌发能力;镉胁迫下则表现为低浓度促进高浓度抑制。随着铅胁迫浓度的升高,马齿苋体内可溶性蛋白、可溶性糖、游离脯氨酸含量和超氧化物歧化酶、过氧化物酶、过氧化氢酶活性下降;而随着镉胁迫浓度的升高,渗透调节物质含量和抗氧化酶活性则呈先升高后降低的趋势。     

红鳞蒲桃苗木生长和生理生化特征对不同盐分和干旱胁迫的响应

以1年生红鳞蒲桃盆栽苗木为研究对象,设置不同盐胁迫浓度及干旱程度,研究盐旱交互作用对红鳞蒲桃苗木的高、地径生长和各项生理指标的影响。结果表明：干旱和盐胁迫都抑制了红鳞蒲桃的生长,盐胁迫的影响要大于干旱胁迫,高生长受到的限制大于地径生长,2 g/kg盐分浓度在水分充足条件下促进了地径生长。相对电导率和丙二醛含量均随着干旱和盐胁迫的增强而增大。不同盐分浓度下,干旱胁迫对相对电导率的影响趋势一致,不同盐分胁迫的影响差异不显著。高盐浓度下丙二醛含量的增加显著大于低盐浓度,表明盐胁迫对红鳞蒲桃的伤害更大;红鳞蒲桃的渗透调节物质在干旱和盐交互胁迫下有一定程度的提高。水分充足时,盐分浓度的变化没有对红鳞蒲桃的游离脯氨酸含量产生影响。随着胁迫的增加,渗透调节能力显著提高。低盐浓度下,抗氧化酶活性在水分充足时没有受到显著影响,高盐浓度下,随着干旱胁迫的加剧则显著提高。     

1986—2016年黄河三角洲土地利用/覆被变化及景观格局分析

基于Landsat影像获取1986年、1996年、2006年和2016年的土地利用/覆被变化数据,使用变化轨迹模型和景观格局指数研究黄河三角洲近30年土地利用/覆被结构变化、变化轨迹时空特征及景观格局。结果表明：1996—2016年黄河三角洲耕地、人工水体、建设用地面积呈增加趋势,未利用地、林地、草地和天然水体面积减少,其中未利用地面积减少2 072.75 km²,变化幅度最大。人工水体、建设用地及耕地的增加速度不断减缓;草地和天然水体于1986—1996年缓慢增加,1996年后持续减少;林地、未利用地在3个时段均呈快速减少趋势。“人为因素”驱动轨迹面积占研究区总面积的56.13%,主要类型变化为耕地与人工水体,分布在河流两侧和滩涂向陆一侧;“自然因素”驱动轨迹占比15.80%,主要类型为变化为海域、草地和天然水体,集中分布在北部和东部沿海地区;研究区28.07%的土地利用/覆被类型未发生变化。黄河三角洲“人为因素”驱动轨迹的景观破碎度、集聚程度和结构复杂程度均高于“自然因素”驱动轨迹,人类活动在研究区土地利用/覆被变化过程中起主导作用。该研究结果可为黄河三角洲土地资源开发、管理与保护提供参考。     

烟草田间起垄机作业适应性研究

对开沟式和盒式的1WG-6.3型自走式小型起垄机进行田间试验,并对其作业效益、作业效率及作业效果等指标进行测量及性能分析对比。结果表明:盒式起垄机每公顷平均油耗较低,作业效率较高,稳定性好,起垄效果较好,能满足烤烟种植起垄效果的农艺要求;开沟式起垄机能满足烤烟种植垄底宽、垄高的农艺要求,但不能满足烤烟种植垄基宽的农艺要求,且每公顷平均油耗较高,作业效率较低,稳定性较差,垄形一般。因此,盒式起垄机更能适应烟草田间起垄作业。     

HSP90 gene expression induced by aspirin is associated with damage remission in a chicken myocardial cell culture exposed to heat stress

1. To understand the potential protection of heat shock protein 90 (HSP90) induced by aspirin against heat stress damage in chicken myocardial cells, enzyme activities related to stress damage, cytopathological changes, the expression and distribution of HSP90, and HSP90 mRNA levels in the myocardial cells exposed to heat stress (42°C) for different durations with or without aspirin administration (1 mg/ml, 2 h prior) in vitro were investigated.

2. Significant increase of enzyme levels in the supernatant of heat-stressed myocardial cells and cellular lesions characterised by acute degeneration, karyopyknosis and karyorrhexis were observed, compared to non-treated cells. However, the lesions of cells treated with aspirin were milder, characterised by earlier recovery of enzyme levels to the control levels and no obvious heat stress-related cellular necrosis.

3. Stronger positive signals in the cytoplasm and longer retention of HSP90 signal in nuclei were observed in aspirin-treated myocardial cells than those of only heat-stressed cells. HSP90 level in the aspirin-treated myocardial cells was 11.1-fold higher than that in non-treated cells, and remained at a high level at the early stage of heat stress, whereas it was just 4.1-fold higher in only heat-stressed cells and returned rapidly to a low level.

4. Overexpression of HSP90 mRNA in aspirin-treated cells was observed throughout the experiment, whereas HSP90 mRNA decreased significantly only in heat-stressed cells.

5. The early higher HSP90 expression induced by aspirin during heat stress was accompanied by decreased heat stress damage, suggesting that aspirin might play an important role in preventing myocardial cells from heat stress damage in vitro.

     

亚美马褂木不同生根类型硬枝扦插苗生长研究

以珍珠岩基质中亚美马褂木硬枝扦插苗为研究对象,研究了扦插苗生根类型、不定根数、不定根长、苗高、基径、鲜样质量和根芽距等生长指标,为选择高生长和高生根率无性系提供参考。结果表明:亚美马褂木扦插苗不定根形成有3种生根类型即皮部生根类型、中间生根类型和愈伤生根类型,其中愈伤生根类型扦插苗成活数量多,中间生根类型扦插苗生长最好,愈伤生根类型扦插苗生长较好。扦插苗鲜样质量与不定根数、不定根长、苗高和基径等相关系数达极显著正相关,苗高与不定根数和基径、不定根数与基径等相关系数达极显著正相关,不定根数与生根类型相关系数达极显著负相关。     

Stepwise in-straw dilution and direct transfer using open pulled straws (OPS) in the mouse: a potential model for field manipulation of vitrified embryos

In the present study, mouse blastocysts were employed to investigate the feasibility and efficiency of stepwise in-straw dilution and direct transfer using the open pulled straw (OPS) method. In experiment I, the effects of various vitrification solutions (VS) on embryo survival were examined. After thawing, the expanded blastocyst rates (97.59 and 95.05%) and hatching rates (80.48 and 78.95%) achieved in the EDFS30 [15% ethylene glycol (EG), 15% dimethyl sulfoxide (DMSO), Ficoll, and sucrose] and EFS40 [40% EG, Ficoll, and sucrose] groups were no different from those (96.15% and 83.33%) of the control group. However, the rates in the EFS30 [30% EG, Ficoll, and sucrose] (87.80 and 55.43%) and EDFS40 [20% EG, 20% DMSO, Ficoll, and sucrose] (95.69 and 70.97%) groups were significantly lower than those (96.15 and 83.33%) of the control group (P<0.05). In the experiment II, the effects of the volume of VS in the OPS on the survival of embryos after in-straw thawing were investigated. When the length of the VS in the column was less than 1 cm, the in vitro viability of embryos thawed by stepwise in-straw dilution was no different among the experimental and control groups. The embryos could be successfully thawed by immersing the OPS in 0.5 M sucrose for 3 min and then 0.25 M sucrose for 2 min. In experiment III, the effect of immersion time of the OPS in diluent (PBS) on the viability of vitrified embryos was investigated. After in-straw thawing, OPSs were immersed immediately in 1 ml PBS for 0 to 30 min. When the immersion time of the OPSs in PBS was less than 12 min, in vitro development of the in-straw thawed embryos was no different from that of the controls. In experiment IV, in-straw thawed blastocysts were directly transferred to pseudopregnant mice to examine their in vivo developmental viability. The pregnancy (91.67%) and birth rates (42.42%) of embryos in-straw thawed and directly transferred were no different from those of the unvitrified controls (90.90 and 40%) and embryos thawed by the conventional method (84.61 and 46.94%). These results demonstrate that mouse embryos vitrified with OPS could be successfully thawed by stepwise in-straw dilution and transferred directly to a recipient and that this method might be a model for field manipulation of vitrified embryos in farm animals.