去雄对睡莲花瓣开放角度及生理生化特征的影响

为揭示睡莲(基部被子植物)的开花特性,探究雄蕊在睡莲花瓣节律性开放过程中的作用.本研究以蓝鸟睡莲(Nymphaea 'Blue Bird')为实验材料,在去雄(摘除雄蕊)后记录花瓣开放角度和萎蔫时间,并于去雄后第6、24、48及72小时测定花瓣的生理生化指标变化.结果 显示,去雄后睡莲花瓣的开放角度小于对照组,在第48小时与对照组开放角度差异最大,达到49.31°,而去雄后花瓣萎蔫的时间与对照组相同,均出现在第72小时;去雄引起了花瓣多项生理生化指标发生变化,其中,含水量在第24小时与72小时显著低于对照组,比对照组分别低0.7％与0.9％;可溶性糖含量变化显著,在第24小时和48小时比对照组分别高出0.48与0.68 mg/g;脯氨酸(Pro)含量在第72小时显著高于对照组;过氧化物酶(POD)活性从第24小时起比对照组显著升高;而丙二醛(MDA)含量则与对照组无明显差异.以上结果说明,去雄导致了睡莲花瓣开放角度及生理状态发生改变,该发现进一步地揭示了睡莲的开花特性,首次证明了雄蕊对于花瓣节律性开放具有调节作用,为花瓣开放闭合及切花保鲜等领域的研究提供了新的思路.     

响应面优化早花忍冬组培苗增殖培养条件

本试验以早花忍冬组培苗的茎段为试验材料,采用Box-Behnken响应面设计法优化早花忍冬茎段继代培养的条件,为早花忍冬组培离体快繁体系建立提供了参考依据.通过单因素试验法确定激素的添加范围,通过响应面优化得到最佳的增殖培养基.结果表明:激素种类对早花忍冬组培苗茎段继代培养的影响顺序依次为:6-BA＞IAA＞IBA,并且在6-BA浓度为1.9 mg/L、IBA浓度为0.76 mg/L、IAA浓度为0.27 mg/L时,茎段继代培养的增殖系数为7.66,与方程预测值相接近.     

太原市五种园林地被植物抗旱性评价及抗旱指标筛选

以5种地被植物为试材,采用盆栽控水模拟干旱胁迫(连续干旱0、5、10、15、20 d),分别测定5种地被植物的叶片相对含水量(RWC)、电导率(REC)、丙二醛(MDA)、可溶性蛋白质含量(SPC),并利用隶属函数分析、相关性分析、主成分分析、聚类分析、逐步回归分析对其抗旱性进行综合评价及抗旱指标筛选,以期为太原市园林地被植物的合理养护和筛选应用提供参考依据.结果表明:干旱条件下,不同生理指标所反映供试植物的抗旱性不同,且部分指标之间呈显著相关.主成分分析将12个单项指标归纳成3个综合因子,分别为伤害程度因子、叶绿素因子、水分状况和光化学效率因子,代表了抗旱性97.422％的数据信息,"金冠"玉簪和德国鸢尾分别在3个主因子上抗旱性最强.通过聚类分析,将5种地被植物分为3类,其中"金冠"玉簪、德国鸢尾和八宝景天归为抗旱型类群.逐步回归分析表明,RWC、离体叶片失水速率(RWL)、SPC和PSⅡ最大光化学效率(Fv/Fm)可作为评价参试地被植物抗旱性的重要指标.     

天津春稻和麦茬稻品质特性比较

以天津市培育的优质小站稻品种津川1号和隆优619为供试材料,分析了春稻和麦茬稻品质特性的差异。结果表明,津川1号作麦茬稻的整精米率明显低于作春稻,而垩白粒率显著高于春稻;津川1号麦茬稻的蛋白质含量明显偏高,食味值显著低于春稻;隆优619作春稻和麦茬稻无论在外观、加工、食味还是营养品质方面均无显著差异,是较理想的麦茬连作品种。     

岩溶流域典型农业区水体氢氧同位素的空间异质性及形成机制

分别于平水期和枯水期采集了花溪河流域典型农业区地表水和地下水样品。利用氢氧同位素示踪技术,结合土地利用类型对研究区不同水体的补给来源、季节变化及主要影响过程进行了分析,并对不同水体氢氧同位素值进行了空间插值分析,同时对其形成机制进行了分析,阐明了不同土地利用类型影响下的主要水文过程。结果表明:(1)研究区不同水体的主要补给来源为当地大气降水,月亮湖水库受蒸发作用影响明显,地表水和地下水的δD和δ~(18)O整体上呈现平水期高于枯水期的特征。(2)地下水的δD和δ~(18)O在枯水期与平水期均呈现明显的空间分异性特征,西部水田/水库集中区富集,东部旱地集中区贫化,土地利用对研究区环境水文过程影响明显。该研究结果有助于了解不同土地利用方式下地表水对地下水的影响,为流域管理提供科学依据。     

基于NB-IoT架构的分布式配电自动化系统

文章主要介绍了基于NB-IoT物联网模块的智能分布式配电自动化系统的系统构建原理概述,其中对智能分布式配电自动化系统与NB-IoT物联网模块的系统应用和分布式软件边缘计算进行了详细阐述和说明。     

软枣猕猴桃叶片愈伤组织诱导技术的研究

[目的]由于软枣猕猴桃在初代培养中外植体诱导率极低且快繁效果差,因此进行其组织培养技术体系的研究,以期解决其人工种植的难题.[方法]本研究以软枣猕猴桃展叶为外植体,通过采用不同消毒试剂及消毒处理时间,筛选出最佳的灭菌程序;将不同培养基与不同浓度的KT、2,4-D组合,筛选出最佳的初代培养基配方.[结果]选用展叶为外植体,75％CH3CH2OH处理30 s后以10％NaClO处理20 min,0.1％HgCl2处理15 min后无菌水冲洗3～4次,接至pH=5.8的MS+1 mg·L-1 KT+0.5 mg·L-12,4-D+3％白糖+0.55％琼脂培养基上,置于光照2500 lx、8 h·d-1,26℃下培养8 d后有少部分愈伤组织出现,60 d后平均单芽愈伤组织达0.8 g以上,平均单个愈伤组织长度0.7～1.4 cm,属中块愈伤组织.[结论]以本实验得出的愈伤组织培养方法进行培养,可有效提高诱导率,达到快繁的目的.     

Screening and Verification of Low Nitrogen Tolerant and Nitrogen Sensitive Cotton Germplasm

[Objective] The aim of this study is to evaluate nitrogen efficient cotton germplasms and improve nitrogen use efficiency. [Method] Eighty cotton germplasms were selected and evaluated in the hydroponic experiment under low (0.25 mmol·L^－1) and high (5 mmol·L^－1) nitrogen concentration. Different traits for screening were identified and nitrogen use efficiency types were classified. Field experiments were also performed for comparison and confirmation of the identified germplasms. [Result] The results showed that there were significant differences in the total plant dry matter, shoot nitrogen accumulation and nitrogen absorption efficiency in cotton germplasms at the two nitrogen levels. Based on coefficient of variation, principal component analysis and correlation, six traits including total plant dry matter, shoot dry matter, root dry matter, total nitrogen accumulation, shoot nitrogen accumulation and nitrogen absorption efficiency were used as screening indicators. According to the Heatmap clustering analysis and the nitrogen efficiency comprehensive index, two germplasms (Lu05R59 and CCRI 69) were identified as low nitrogen tolerant and nitrogen efficient, and two germplasms (Coker 201 and Xinluzhong 30) as low nitrogen sensitive and nitrogen inefficient. The results of field experiment were consistent with the results of the hydroponic culture at the seedling stage. [Conclusion] It was finally determined that Lu05R59 and CCRI 69 were the low nitrogen tolerant and nitrogen efficient germplasms, and Coker 201 and Xinluzhong 30 were low nitrogen sensitive and nitrogen inefficient germplasms. The results of these studies provide the possibility for screening and rapid identification of nitrogen use efficiency in cotton at the seedling stage, and provide the ideal materials and theoretical basis for further study of cotton nitrogen efficient.     

外源NO及反向调控PEG胁迫下苜蓿萌发种子抗氧化酶及其同工酶动态的研究

以紫花苜蓿为材料,用一氧化氮供体硝普钠(SNP)及一氧化氮清除剂c-PTIO对苜蓿种子进行浸种处理,采用分光光度法和同工酶电泳技术来研究外源NO及反向调控对PEG胁迫下紫花苜蓿抗氧化酶活性及其同工酶的影响,并探讨NO调控苜蓿种子耐旱性的生理机制。结果表明:PEG胁迫下外施0.1 mmol·L^-1 SNP,第6天时较PEG处理POD活性降低了32.72%;第4天时SOD、CAT活性较PEG处理升高了10.48%、23.60%,有效缓解了PEG对紫花苜蓿萌发中种子的氧化损伤,提高其抗氧化能力。PEG胁迫下添加 c-PTIO抑制了苜蓿萌发期的抗氧化系统活性。从同工酶的谱带数量和强弱来看,POD同工酶各区带活力均随PEG胁迫时间的延长而增加,在第2天酶带只有1条,而第4天酶带呈现9条;SOD和CAT同工酶表达量变化不显著,但酶带强弱有一定变化,S3酶带随处理时间的延长表达量逐渐减弱;CAT同工酶谱带则一直保持2条带,无明显强弱变化。因此,外源NO在PEG胁迫下紫花苜蓿萌发中抗氧化酶快速响应并在维护氧自由基代谢平衡中起重要保护作用。     

Differential regulation on C5 expression in goose versus mammals by glucose/palmitate provides a potential protection for goose fatty liver

Goose fatty liver is a specific type of nonalcoholic fatty liver that is protected from harmful effects associated with severe steatosis. Our previous findings suggest that suppression of the complement C5 may be relevant, but the mechanism is unclear. Therefore, in this study, we first verified the expression pattern of complement genes (including C5) during goose fatty liver formation and then determined the liver fat content and fatty acid composition by high-performance liquid chromatography (HPLC), followed by selecting the differential metabolites to treat HepG2, goose and mouse primary hepatocytes, aiming to explore the mechanism of C5 and inflammation suppression in goose fatty liver. The data confirmed the suppression of complement genes (including C5) in goose fatty livers. Moreover, fat content was significantly higher in fatty liver versus normal ones, with oleic acid and palmitic acid dominantly accounting for the difference. In line with this, high concentration of palmitate led to down regulation of C5 expression in goose primary hepatocytes whereas upregulation in mouse primary hepatocytes and HepG2 cells. In conclusion, regulation on C5 expression by fatty liver related factors including high level of palmitic acid may contribute to the protection of goose liver from severe hepatic steatosis.