利凉处理对大棚环境、秋番茄生长与结果及其茎基腐病的影响

为验证利凉的应用效果,采用大田试验方法,研究利凉处理下大棚环境、秋番茄生长、结果和茎基腐病的状况。结果表明：在晴天和阴天条件下,利凉处理棚膜均起到降低大棚内的地温、气温和光照强度的作用,同时可提高大棚内的空气相对湿度,为秋番茄生长提供良好的环境条件。与对照大棚相比,利凉处理大棚提高了秋番茄植株的生长速率,可使秋番茄第一花序坐果率提高18.51%,第一层果实产量提高82.66%,同时可降低大棚秋番茄茎基腐病的发病率达15.28%。综上,利凉可以在大棚秋番茄生产上应用。     

兜兰花粉活力及柱头可授性探究

本研究以‘绿肉饼’兜兰为试验材料,用扫描电子显微镜对其花粉块进行研究分析。结果显示,花粉块可分为两半,表面光滑呈现紧密网状结构。为获得‘绿肉饼’人工授粉最佳时间,采用TTC (氯化三苯基四氮唑)染色和联苯胺-过氧化氢法进行花粉活力及柱头可授性的研究。TTC染色法结果表明,‘绿肉饼’的花粉活力呈现从弱到强再到弱的趋势,其中开花15~20 d的花粉活力最大,授粉率较高;联苯胺-过氧化氢法结果表明,‘绿肉饼’的柱头可授性随开花时间先弱后强再变弱,其中开花10~20 d的柱头可授性最高。     

欧美国家针叶树容器苗生产与启示

针叶树是芬兰、瑞典、挪威、美国、加拿大等欧美国家主要的商品林树种。容器苗是针叶树重要的育苗类型。与裸根苗比较，容器苗具有育苗周期更短、造林季节可延长、苗木适应性更广、苗木质量更一致的优点。因此，容器育苗成为精准林业发展的必然趋势。为了借鉴欧美容器育苗的技术方法，提高我国容器苗的质量，为我国针叶树容器苗发展提供参考，文中主要从4个方面综述了欧美国家检测与提高苗木质量的方法，即列举了针叶树常用的苗木质量检测指标，总结了育苗容器与育苗基质的改良进展，介绍了养分、水分、光照与温度等培养条件的优化手段，简要概述了容器苗病虫害防控的进展，提出了我国相关树种容器苗生产的启示与借鉴。     

芦笋种植对冷凉沙化区土壤改良的效果研究

为探索芦笋种植对冷凉沙化区土壤的改良效果,在山西省朔州市右玉县,以未种植芦笋裸沙地为对照（CK）,设置种植芦笋1、2、3和4年共4个处理,通过田间试验测定不同种植年限芦笋田土壤理化特性和芦笋生长发育情况。结果表明,与CK相比,随种植年限增加,土壤黏粒和粉砂粒含量递增,砂粒含量递减,土壤容重递减,土壤田间持水量递增;土壤pH和可溶性盐浓度（EC）递减;土壤有机质、全氮、有效磷和速效钾含量逐年递增。种植芦笋3年的土壤粒级、土壤容重、田间持水量、pH、EC值、土壤肥力发生显著变化;连续种植芦笋4年的土壤黏粒含量较CK增加到29.8%,粉砂粒含量增加到12.6%,砂粒含量降低到57.6%,田间土壤持水量显著提高,土壤容重显著降低,土壤由砂质壤土向砂质黏土转变;土壤pH降低0.75,EC值降低0.08mS/cm;土壤有机质含量增加28.89%,全氮、有效磷和速效钾含量分别增加95.12%、94.92%和45.40%;芦笋产量达6 037.5kg/hm ²。综合分析,连续种植芦笋4年可改善沙化土壤的物理结构,提高土壤养分,降低盐碱程度。芦笋是冷凉沙化区土壤改良的先锋作物之一,可实现生态效益与经济效益并举。     

F-box domain is involved in regulating the proliferation of MCF-7 cells by FBXO39 protein

AIM: To investigate the effect of F-box domain on the regulation of MCF-7 cell proliferation by FBXO39 protein. METHODS: The effect of F-box domain on the localization of FBXO39 protein in the MCF-7 cells was investigated. MCF-7 cell cDNA library was used as the template resource. The full-length cDNA sequence of FBXO39 was amplified by PCR method and subcloned into eukaryotic expression vector pEGFP-C2. The pEGFP-FBXO39ΔF (F-box domain deletion mutation) plasmid was successfully constructed with the template resource of pEGFP-FBXO39 plasmid. The recombinant plasmids were transfected into the MCF-7 cells, and then the expression of FBXO39 and FBXO39ΔF were determined by Western blot. The cellular localization of FBXO39 and FBXO39ΔF were observed by confocal microscopy. The localization of endogenous FBXO39 in the MCF-7 cells was detected by immunofluorescence staining. In addition, MTT and EdU assays were used to measure the cell proliferation, flow cytometry was used to measure the cell cycle distribution, and immunohistochemical staining was used to observe the expression of FBXO39 in the breast cancer and para-carcinoma tissues. RESULTS: The eukaryotic expression vector pEGFP-FBXO39 and pEGFP-FBXO39ΔF were constructed successfully. F-box domain had no effect on the cell localization of FBXO39. FBXO39 promoted MCF-7 cell proliferation but FBXO39ΔF did not. FBXO39 was highly expressed in the breast cancer tissues. CONCLUSION: F-box domain had no effect on the cellular localization of FBXO39 protein. However, it plays an important role in the biological function of FBXO39. FBXO39 may be related to breast cancer tumorigenesis.     

1969-2018年黄河实测径流与天然径流的变化

[目的] 分析黄河实测径流与天然径流的变化规律，为探究人类活动对径流的影响提供依据。[方法] 基于1969—2018年黄河干流8个水文站的天然径流和实测径流数据，使用Mann-Kendall趋势检验与突变检验法，对比分析近50 a黄河干流实测径流和天然径流的变化规律。并结合近15 a各分区耗水数据探讨人类活动对于径流的影响。[结果] ①1969—2018年黄河上中下游实测径流整体呈降低趋势，兰州、花园口、利津3个代表站多年平均降低速率分别为5.10×10⁷，3.55×10⁸，4.13×10⁸ m³/a。②近50 a天然径流和实测径流趋势突变主要集中在1986和1990两个年份，结合前人研究和重要水事分析，1986年突变可能与1984年以来一系列水土保持措施实施以及1986年龙羊峡水库修建有关；而造成1990年径流突变的原因可能是80—90年代黄河流域用水量激增和流域下垫面改变。③天然径流与实测径流的差值从上游至下游水文站断面逐渐增大，这主要与近15 a平均耗水量也沿程增大相一致；另外多年平均实测径流在利津站仅占天然径流的42%。耗水量最大的两个分区为花园口以下和兰州—头道拐段，分别达到了1.06×10¹⁰和1.04×10¹⁰ m³。[结论] 人类活动中的各项耗水（尤其是农田灌溉）是造成兰州站以下地区天然径流与实测径流差值大的主要原因，因此，应进一步推进黄河流域节水农业的发展，合理分配各项耗水量。     

Effects of fish meal replaced by fermented soybean meal on growth performance,intestinal histology and microbiota of largemouth bass (Micropterus salmoides)

This study was conducted to investigate the effects of replacing fish meal (FM) with fermented soybean meal (FSM) and soybean meal (SM) on growth performance, intestinal histology and microbiota of largemouth bass (Micropterus salmoides). The basal diet contained 350 g/kg FM (CON), and then, FM was replaced with SM and FSM at the ratios of 30% and 60% (SM‐30, SM‐60, FSM‐30 and FSM‐60), respectively. The largemouth bass (4.43 ± 0.13 g) were fed for 8 weeks. The results showed that weight gain of fish fed with FSM‐60 and SM‐60 diets was significantly lower, and feed conversion ratio of SM‐30, SM‐60 and FSM‐60 groups was significantly higher than the CON group (p < .05). The intestinal villus height of SM‐60 group and the villus width of SM‐60 and FSM‐60 group were significantly lower than the CON group (p < .05). The 30% FM replacement by SM and FSM significantly increased the abundance of Cetobacterium and Mycoplasma, respectively (p < .05). In conclusion, FSM could replace 30% FM in diet without negative impacts on the growth performance of largemouth bass, while the SM should be controlled below 30%.     

Characterization and expression of SLO1 potassium channels during spermatogenesis in Eriocheir sinensis

SLO1 potassium channels are pivotal to many aspects of spermatogenic cell. Experiments were conducted to assess physiology and function of SLO1 potassium channels in different developmental stages of spermatogenic cell in Eriocheir sinensis. First, the expression of SLO1 protein was examined via Western blot, RT‐PCR, immunohistochemistry and immunofluorescence assays. The results showed that the expression of the SLO1 protein was not uniform in the spermatogenic cells of E. sinensis. Second, whole‐cell patch clamp technique was used to record the potassium current of spermatogenic cells and to analyse the electrophysiological characteristics of the potassium channels with the aid of inhibitors. It is proved that the potassium current in E. sinensis germ cells is associated with intracellular Ca²⁺, and the calcium‐activated potassium channel mediated by SLO1 protein is mainly large‐conductance Ca²⁺‐activated K⁺ channels (BK_Ca). Based on these researches, the cDNA of SLO1 from testis was cloned and sequenced. The SLO1 protein contained domains bound to calcium ions, and the spatial structure formed by its tetramers constituted potassium channels. Phylogenetic analysis revealed that SLO1 was much closer to Scylla paramamosain than other examined species. Finally, iberiotoxin (IbTX) and CdCl₂ were used to inhibit the acrosome reaction (AR) induced by A23187 and to explore the role of SLO1 potassium channels in the AR of E. sinensis. The experimental results showed that SLO1 potassium channels were expressed in E. sinensis spermatogenic cells and played an important role in the AR of crab sperm (SP).