串番茄新品种红星302 的选育

红星302 是以抗病、耐低温弱光材料01-61 为母本，以01-23 为父本育成的串番茄一代杂种，无限生长类型，果实串收，果色亮红，果实椭圆形，酸甜适口，品质佳，VC 含量为364 mg · kg^-1，可滴定酸0.44%，可溶性糖4.25%，平均单果质量30.79 g，硬度为11.40×10⁵ Pa。单株结果数约为53个，产量4 900 kg ·（ 667 m²）^-1 左右，高抗蕨叶病毒病、青枯病，适宜河北地区冬季日光温室和早春保护地栽培。     

Genome-wide association study for spot blotch resistance in Afghan wheat germplasm

Spot blotch (SB), caused by Bipolaris sorokiniana, is a devastating disease of wheat globally, especially in South Asia and South America. Understanding the genetics of resistance to SB is important for developing breeding strategies to improve resistance. A panel of 301 genotypes from Afghanistan was phenotyped over two crop seasons using a mixture of virulent B. sorokiniana isolates and genotyped using DArTSeq to obtain genome-wide markers. Fifty genotypes (16.6%) showed disease scores less than the resistant control. Principal component analysis using the genotypic data clustered the genotypes into five different groups. Among models used for genome-wide association mapping, the multilocus mixed model, and fixed and random model circulating probability unification algorithms were most effective in identifying significant marker-trait associations (MTA). Twenty-five MTAs at p ≤ .001 were identified on chromosomes 1A, 1B, 1D, 2B, 2D, 3A, 3B, 4A, 5A, 5B, 6A, 7A, and 7D, indicating the quantitative nature of resistance to SB. Phenotypic variation explained by these markers ranged from 2.0% to 17.7%, and genomic regions on the chromosomes 1D, 2D, 3A, 3B, 4A, 5A, and 5B coincided with loci identified in previous studies. Three single nucleotide polymorphism (SNP) markers on chromosomes 1B (SNP 1113207) and 5A (SNPs 5411867 and 998276) were significant in both crop seasons as well as in the combined analysis across seasons. Marker 5411867 is close to Vrn-A1, shown to be associated with SB in previous studies. Furthermore, among known SB resistance genes, Sb2 on chromosome 5B was predicted to be significant in this panel.     

生态系统服务权衡最新研究进展

生态系统服务权衡研究对协调生态环境保护和社会经济发展至关重要。为推动生态系统服务管理和提升人类福祉,本文以Web of Science核心合集(WOS)和中国科学引文数据库(CSCD)为数据源,运用文献计量分析法,系统梳理和总结生态系统服务权衡研究的学科知识基础、科学领域结构和热点变化等发展现状以及最新研究进展。研究表明:1)不同研究层面上,生态系统服务间的权衡关系受外部风险和人类需求、参数选取和服务提供者及区域差异性和不均衡性的影响。2)研究方法主要有基于关系识别和具体表征的权衡分析、权衡模拟和预测的模型量化分析和生态系统服务权衡管理优化的多准则分析3类。3)生态系统服务权衡关键驱动因子为城市化、生态工程和气候变化。基于此,我们认为把握生态系统服务权衡不同研究层面的关联特征、创新和优化生态系统服务权衡研究方法、准确甄别生态系统服务权衡关键驱动因子以及充分整合多维生态系统服务权衡资源搭建数据共享平台是未来研究的重点。     

川麦42和川农16抗穗发芽QTL定位及聚合效应分析

【目的】小麦穗发芽严重影响小麦产量和品质,是全球小麦生产面临的重大问题之一。通过鉴定挖掘抗穗发芽QTL,聚合穗发芽抗性位点,选育抗穗发芽小麦品种,为四川小麦穗发芽抗性改良提供技术和材料支撑。【方法】以川麦42/川农16重组自交系（RIL,F₈）为材料,于2016—2018年分别在2个环境下对RIL群体进行籽粒发芽指数（GI,2016和2018）、籽粒发芽率（GR,2016和2018）和整穗发芽率（SGR,2017和2018）3个穗发芽指标测定。利用90K SNP芯片构建的遗传图谱检测全基因组穗发芽相关QTL,并分析抗性QTL聚合效应。【结果】双亲间GI、GR和SGR指标值差异显著,亲本川农16穗发芽抗性明显优于亲本川麦42。共检测到11个与穗发芽抗性有关的QTL,主要分布在2B、2D、3A、3D、4A、5A、5B和6B染色体上。5B染色体上检测到的单个环境表达的整穗发芽QTL解释的表型变异率最大,达到29%;在2D和3A染色体上检测到的整穗发芽主效QTL,以及5A染色体上检测到的与种子休眠相关的籽粒发芽主效QTL,在2个环境下均能表达,其抗穗发芽等位变异均来源于川农16。基因型分析发现,RIL群体中不同株系聚合抗性QTL的数量变幅为1—9个,表现为抗穗发芽的株系均携带4—9个与穗发芽相关的抗性QTL。重组自交系群体中6个株系GI、GR和SGR值均在15%以下,表现出高抗穗发芽特性;这6个优异株系聚合了多个与穗发芽相关的抗性QTL,且均聚合了川麦42在4A染色体上的微效QTL（QGi.saas-4A和QGr.saas-4A）,以及川农16在2D和5B染色体上的主效QTL（QSgr.saas-2D和QSgr.saas-5B）;编号为104和125的优异株系已通过审定,定名为川麦104和川麦64。其中,川麦104于2012年同时通过国家和四川省审定,其抗穗发芽能力强,产量、品质、抗病等优良性状突出,聚合了7个正向穗发芽QTL,包括2B、2D和5B染色体上来源于川农16的4个抗性QTL（QGi.saas-2B、QGr.saas-2B、QSgr.saas-2D和QSgr.saas-5B）,以及4A和6B染色体上来源于川麦42的3个QTL（QGi.saas-4A、QGr.saas-4A和QGr.saas-6B）;近年来,川麦104已成为西南麦区小麦育种的核心亲本,育成小麦品种（系）18个。【结论】共检测到11个抗穗发芽QTL,其中3个来源于川麦42,8个来源于川农16;RIL群体中的抗穗发芽株系均携带4—9个抗性QTL,优异株系川麦104和川麦64高抗穗发芽,均聚合了7个穗发芽抗性QTL。     

优化施肥下长江流域冬小麦产量及肥料增产效应

【目的】针对长江流域冬小麦不合理施肥带来的肥料利用率低的现状,探讨冬小麦产量分布特征及施用氮、磷和钾肥料的增产效应,为长江流域冬小麦肥料减施增效和优化养分管理措施提供依据。【方法】本文数据来源于国际植物营养研究所（IPNI）于2000—2018年在我国长江流域开展的田间试验,以及在中国知网（CNKI）数据库通过检索字段或字段组合（冬小麦、冬小麦+产量及冬小麦产量+肥料利用率等）得到的此期间关于长江流域冬小麦田间试验的论文,共1 732个田间试验。试验处理包括：优化施肥处理,农民习惯施肥,以及在优化施肥和农民习惯施肥基础上的不施氮肥、不施磷肥和不施钾肥处理,以探究长江流域各省（市）（四川、云南、贵州、重庆、湖北、安徽、江苏、浙江和上海）冬小麦在优化施肥下的可获得产量、产量反应、相对产量、农学效率和偏生产力特征。【结果】我国长江流域冬小麦优化施肥处理下的平均产量为6.6 t·hm^-2,其中安徽省平均产量水平最高,为7.3 t·hm^-2,重庆市最低,为3.6 t·hm^-2。施用氮、磷和钾肥的平均产量反应分别为2.3、0.9和0.6 t·hm^-2,但变异范围较大。氮、磷和钾肥平均相对产量分别为0.6、0.8和0.9,氮是小麦产量的主要限制因子。优化施肥处理的氮、磷和钾肥的平均农学效率分别为12.6、11.6和7.7 kg·kg^-1,平均偏生产力分别为34.0、78.9和73.4 kg·kg^-1。与农民习惯施肥措施相比,优化施肥处理平均增产0.5 t·hm^-2,增幅为8.8%;氮、磷、钾肥的农学效率分别提高了41.1%、121.1%和84.6%;偏生产力分别提高了42.4%、23.5%和25.4%。【结论】优化施肥有效提高了长江流域冬小麦的产量和养分利用率,但各省（市）间存在一定差异且省（市）内变异较大。四川、云南、湖北和江苏省的部分地区具有较低的产量反应,说明具有较高的土壤养分供应,应因地制宜地制定养分优化管理方案。分析长江流域优化养分管理措施下的小麦产量反应和肥料利用率等参数,可以确定氮为小麦产量的第一限制因子。     

甘肃、青海地区小麦条锈菌监测及群体遗传多样性分析

【目的】了解甘肃和青海小麦条锈菌（Puccinia striiformis f. sp. tritici）春季流行传播路线、群体遗传多样性和生殖模式,明确春季流行期两省小麦条锈菌的传播关系及菌源交流规律,进而为两省小麦条锈病的预测预报、确定越夏初始菌源来源和有效治理提供理论依据。【方法】选择条锈病常发生的地区作为调查和研究区域。甘肃省4个试验点：陇南市文县、陇东平凉市崆峒区、中部麦区定西市临洮县、临夏州临夏县;青海省2个试验点：西宁市城北区、海东市互助县。2017年秋季,在甘肃和青海省6个试验点内根据当地小麦播种适期依次种植82份变异观察圃材料。2018年4—8月,对试验点82份变异观察圃材料进行田间病害调查,并采集到551份小麦条锈菌标样,使用15对引物进行SSR分子标记分析。利用GenAlEx和POPPR v2.5.0软件对数据进行相关分析, 不显著的rbarD值表示连锁平衡,用于推断群体是否发生有性重组。【结果】82份变异观察圃材料在甘肃地区发病比青海地区严重。15对引物组合共扩增出81个位点,每对引物组合产生的多态性位点为2—12个。551份样本克隆矫正后,共鉴定出505个多位点基因型（MLG）,其中仅有32个MLG被克隆并进行了2—6次重新采样。甘肃和青海群体总的基因型多样性（G=0.917）较高,其中,甘肃平凉群体的最高,青海互助群体次之,甘肃临洮群体最低。小麦条锈菌的遗传变异主要在各群体内部个体之间。春季流行期,菌源在各群体之间交流频繁,青海东部（互助和西宁）群体与甘肃（平凉和临夏）群体之间的基因流高于青海（互助和西宁）群体与甘肃文县群体之间的基因流。最小时空网络图（MSN）和非参数主成分分析（DAPC）表明青海互助和西宁的群体与来自于甘肃平凉和临夏的群体之间菌源关系最密切,差异最小;与临洮群体遗传距离相对较远且临洮群体相对独立;文县群体则是一个完全独立的群体,与其他5个群体之间的差异最大。连锁不平衡分析表明,甘肃文县、临夏和青海西宁群体存在不显著的rbarD值表示连锁平衡,是有性生殖群体,其中文县群体（rbarD=0.0139,P=0.186）显示出明显的有性重组特征。【结论】小麦条锈病春季流行期,甘肃地区与青海东部地区的传播路线以甘肃平凉、临夏到青海的传播为主,甘肃文县到青海的传播为辅。甘肃文县、临夏和青海西宁3个群体存在有性生殖现象,对甘肃、青海地区条锈菌丰富的遗传多样性的形成具有一定作用。     

基于CNN的小麦籽粒完整性图像检测系统

为了快速、准确识别小麦籽粒的完整粒和破损粒,设计了基于卷积神经网络(CNN)的小麦籽粒完整性图像检测系统,并成功应用于实际检测中。采集完整粒和破损粒两类小麦籽粒图像,对图像进行分割、滤波等处理后,建立单粒小麦的图像数据库和形态特征数据库。采用LeNet-5、AlexNet、VGG-16和ResNet-34等4种典型卷积神经网络建立小麦籽粒完整性识别模型,并与SVM和BP神经网络所建模型进行对比。结果表明,SVM和BP神经网络所建模型的验证集识别准确率最高为92. 25%; 4种卷积神经网络模型明显优于两种传统模型,其中,识别性能最佳的AlexNet的测试集识别准确率为98. 02%,识别速率为0. 827 ms/粒。基于AlexNet模型设计了小麦籽粒完整性图像检测系统,检测结果显示,100粒小麦的检测时间为26. 3 s,其中,图像采集过程平均用时21. 2 s,图像处理与识别过程平均用时为5. 1 s,平均识别准确率为96. 67%。     

Straw mulching with fertilizer nitrogen: An approach for improving crop yield,soil nutrients and enzyme activities

Field experiments were conducted to study soil properties, soil enzymes activities, water use efficiency (WUE) and crop productivity after six years of soya bean straw mulching in the semi‐arid conditions of China. The experiment included four treatments: CK (Control), N (240 kg N ha^‐1), H (soya bean straw mulching at half rate 700 kg ha^‐1 with 240 kg N ha^‐1) and F (soya bean straw mulching at full rate 1,400 kg ha^‐1 with 240 kg N ha^‐1). Soil organic carbon (SOC), soil labile organic carbon (LOC), soil available N (AN), available P (AP) and enzyme activities were analysed after wheat harvesting in 2016 and 2017. Results show that straw amounts had positive effects on the soil fertility indices being higher for treatment F. The SOC, LOC, AN, AP and enzyme activities (i.e. saccharase, urease and alkaline phosphatase) were in the order of F > H > N > CK. High wheat grain yield and WUE were observed for F treatment. A total of six years mulching along with 240 kg ha^‐1 nitrogen fertilizer application is sufficient for wheat yield stability and improving soil properties except urease activities in the semi‐arid condition of China. However, the straw mulching amount should be further studied with minimum nitrogen fertilizer for an environment‐friendly and effective approach for improving the soil biological properties with adequate crop production on a sustainable basis in the semi‐arid region of China.     

Effect of pidotimod on renal function and inflammatory response in rat IgA nephropathy model

AIM:To explore the effect of pidotimod on the renal function in IgA nephropathy (IgAN) rat model, and to further study whether this effect is related to the inhibition of inflammatory response. METHODS:The SD rats (n=36) were randomly divided into control group, IgAN model group, IgAN with prednisone treatment group and IgAN with pidotimod treatment group, with 9 rats in each group. The IgAN model was induced by consecutive oral administration of bovine gamma globulin (BGG) for 8 weeks followed by injection of BGG through tail vein for 3 d. After the IgAN model was established, the drug was continuously used for 4 weeks. At the end of the treatment, the urine protein, serum creatinine and blood urea nitrogen were examined by an automated analyzer. IgA deposition in the renal tissues was observed by immunofluorescence staining. The mRNA expression levels of renal fibrosis markers transforming growth factor-β1 (TGF-β1) and fibronectin 1 in the renal tissues were detected by RT-qPCR. The mRNA and protein levels of pro-inflammatory cytokines interleukin-1β (IL-1β) and IL-6 in the renal tissues were determined by RT-qPCR and Western blot, respectively. RESULTS:No significant difference of the body weight was observed in different groups. Compared with control group, the content of urine protein, serum creatinine and blood urea nitrogen were significantly increased (P<0.01), whereas those were reversed by pidotimod treatment. The results of immunofluorescence staining showed that pidotimod inhibited IgA deposition in the IgAN rats. Pitomod treatment inhibited the mRNA expression levels of renal fibrosis markers TGF-β1 and fibronectin 1, and the mRNA and protein levels of pro-inflammatory cytokines IL-1β and IL-6 in the renal tissues of IgAN rats. CONCLUSION:Pidotimod alleviates IgAN progression in rats by inhibition of inflammatory response.     

Regulatory effect of astragaloside IV on SDF-1α/CXCR4 in EPCs

AIM: To investigate the effects of astragaloside IV (AS-IV) on chemokine receptor 4 (CXCR4) and stromal cell-derived factor 1α (SDF-1α) in endothelial progenitor cells (EPCs) and its mechanism. METHODS: Rat bone marrow-derived EPCs were cultured in vitro. The proliferation, adhesion, migration, apoptosis and tube formation capacity of EPCs treated with AS-IV and AMD3100, a specific blocker of CXCR4, were observed. The effects of AS-IV on the expression of SDF-1α/CXCR4 at mRNA and protein levels and the protein level of p-CXCR4 in the EPCs were determined. RESULTS: AS-IV significantly enhanced the proliferation, adhesion, migration and tube formation abilities of EPCs, reduced the apoptosis of EPCs, and up-regulated the mRNA and protein expression of SDF-1α and CXCR4 and the p-CXCR4 protein level in the EPCs. On the other hand, AMD3100 blocked the up-regulating effect of AS-IV on the mRNA and protein expression of CXCR4 and the p-CXCR4 protein level in the EPCs, but did not affect the effect of AS-IV on the expression of SDF-1α. CONCLUSION: AS-IV might enhance the biological function of EPCs by regulating the expression of SDF-1α/CXCR in EPCs.