基于“言象意”思想的上海方塔园诗意空间营造研究

探析"言象意"思想与园林意境营造之间的联系,总结出立意、取象与尽意的园林意境空间营造方法。以方塔园为例,分析其在立意、取象与尽意等方面的营造手法,证实基于"言象意"思想的营造手法在诗意空间营造中的可行性与实用性,从中得到对现代诗意空间营造的启示:自然与生态精神的追求,传统文化的提取,现代资源的应用与诗性思维的参与。     

龙脑型阴香可蒸生物量预测模型研究

龙脑型阴香（Cinnamomum burmannii chvar. borneol）矮林经营中，企业和农户需预估可蒸 生物量，以便根据加工能力合理安排采收面积。研究以 3~5 年生龙脑型阴香矮林为对象，按照企业收 购标准，统一以 120 cm 为截顶高度、下部枝条全部保留的方法开展采收测定，在同一试验林中，分 别在 3.5 a 生林龄生长期为 1 a 时和 5.5 a 生林龄生长期为 2 a 时测定树高、胸径、冠幅、分枝数和可蒸 生物量 5 个性状。以线性和非线性的方法拟合单株可蒸生物量模型，用 R2、RMSE、AIC、BIC 等指 标评价并筛选出最佳模型，筛选结果是 2 a 生长期最优线性和非线性模型分别 DB=0.625H+0.076HDD， DB=0.091HDD+0.000 017 8HDD2 ，1 a 生长期的分别是 DB=-1.646H-2.734D+4.134C+1.252HD，DB=-1.356 H+0.907H2。4 个模型在实际应用中估算的相对误差分别是 16.680%、14.107%、2.036% 和 20.543%。企业 可依模型估算可蒸生物量，合理安排采收面积。     

2001-2017年天山中段积雪时空变异研究

【目的】为干旱区提供冰雪资源的合理利用及灾害防治的科学理论不服务信息。【斱法】采取趋势分析法、相关性分析法,开展了2001-2017年积雪年内年际变化特征以及分布变化原因斱面的研究。【结果】①天山中段SCP(积雪覆盖率)年际变化呈"单峰"型曲线,6月到最小值,12月到次年1月达到最大值,从2月开始逐渐下降到最小值;从7月初开始SCP开始逐渐上升到最大值。②天山中段年际SCP呈减少趋势、春季的SCP变化呈略微减少趋势、夏季不秋季SCP变化均呈增加趋势、冬季SCP变化趋势跟全年年际SCP变化趋势基本相似,且均呈减少趋势,最高值为98.6%,最小值出现在2009年为83.2%。③天山中段54.08%区域的SCD(积雪日数)呈减少趋势,其中4.36%区域呈显著减少趋势;45.92%区域的SCD呈增加趋势,其中3.03%区域呈显著增加趋势。④天山中段积雪不LST(地表温度)年际相关性呈负相关性比较明显,负相关占总面积的55.89%,主要分布在高海拔的天山山脉,博格达尔;34.98%区域呈极显著负相关,主要分布在伊犁河谷、天山南北坡地区不阿克苏、库尔勒、博斯腾湖流域周边。【结论】天山中段积雪时空变化丌仅是LST变化的影响,还受人类活劢和海拔高度差异等因素的共同作用。     

Role of TLR4-TRPC6 in LPS-induced NF-κB P65 expression and nuclear translocation in airway epithelial 16HBE cells

AIM: To investigate the role of Toll-like receptor 4 (TLR4) and transient receptor potential channel 6 (TRPC6) signaling pathway in lipopolysaccharide (LPS)-induced nuclear factor-κB (NF-κB) P65 expression and nuclear translocation in airway epithelial cells (16HBE) for supplementing the mechanism for airway inflammation. METHODS: After stimulating the 16HBE cells with LPS at 1 mg/L for 0, 0.5, 2, 6, 12 and 24 h, the expression of NF-κB P65 at mRNA and protein levels in the 16HBE cells were determined by RT-PCR and Western blot respectively, and the nuclear translocation of NF-κB P65 was detected by immunocytochemical staining method. The effects of TLR4 inhibitor CLI-095 at 5 μmol/L and TRPC6 agonist Hyp9 at 10 μmol/L on LPS (1 mg/L)-induced NF-κB P65 expression and nuclear translocation in the 16HBE cells were determined by RT-PCR, Western blot and immunocytochemical staining. RESULTS: LPS increased the mRNA and protein expression of NF-κB P65 and nuclear translocation in the 16HBE cells(P<0.05). TLR4 inhibitor CLI-095 reduced the mRNA and protein expression of NF-κB P65 and nuclear translocation induced by LPS, while Hyp9 enhanced the mRNA and protein expression of NF-κB P65 and nuclear translocation induced by LPS in the 16HBE cells(P<0.05). CONCLUSION: LPS induces the expression and nuclear translocation of NF-κB P65 in the 16HBE cells via TLR4-TRPC6 signaling pathway.     

红富士苹果芽变系DNA甲基化研究

以35份富士苹果(Malus×domestica Borkh.‘Fuji’)芽变材料为试材,利用甲基化敏感扩增多态性(Methylation Sensitive Amplified Polymorphism,MSAP)分析和UPGMA聚类方法,对其基因组甲基化修饰水平、变异模式以及表观遗传变异关系进行研究。结果表明:(1)不同富士系得到不同的MSAP扩增,总DNA甲基化水平27.90%～36.16%,平均32.87%,双链全甲基化为主要甲基化方式;(2)富士芽变材料绝大多数位点保持了原有甲基化模式;(3)绝大多数芽变(68.57%)检测到全部的甲基化变异模式(12种),去甲基化频率极显著高于甲基化频率(P 0.01),且CG去甲基化极显著高于CHG;(4)36份种质遗传相似系数平均值0.89(0.79～0.92),在聚类图上,富士原种分布在芽变系集中区外,新近发生的芽变系更倾向于聚在一起,着色系片红型和条红型芽变呈分散排布状态。总的来看,富士芽变的甲基化变异模式丰富,超甲基化和去甲基化相伴发生,但以去甲基化为主;‘富士’着色芽变与其最原始品种富士,以及芽变之间发生了较大表观遗传变异;片红和条红型芽变聚类未表现明显偏好性。本研究将为进一步开展富士着色系芽变机理研究提供指导,可以CG去甲基化为切入点展开深入研究。     

基于温度植被干旱指数的曲靖市干旱监测研究

本研究利用MODIS归一化植被指数(NDVI)和地表温度(Ts)产品数据,构建Ts-NDVI特征空间,计算温度植被干旱指数(TVDI),分析评价云南曲靖市2010—2012年的干旱时空分布状况。结果表明,2010年曲靖市遭遇了非常严重的干旱灾害,受灾面积高达研究区总面积的80%以上,基于TVDI指数的旱情动态监测方法适合云南省曲靖干旱监测。本研究建立的温度植被干旱指数模型提高了干旱监测的实用性,在曲靖市干旱监测上具有很好的适应性,可以广泛应用到该地区干旱监测研究中,为曲靖的农业防灾减灾能力和可持续发展提供科学保障。     

高压雾化设备在现代农业中的应用

高压雾化设备指利用高压雾化主机将经过精密过滤处理的水,输送到造雾专用高压管网,最后到达造雾专用喷头喷出成雾的系统。高压雾化设备在现代农业中主要应用在设施农业降温、加湿、植保以及景观等方面。其中,设施温室降温时依据地域的气候条件、系统投资、后期维护费用、运行费用、降温效果以及对温室湿度的影响等各种因素,来综合考虑高压雾化与其他降温方式联合使用降温,以期达到最佳效果。根据工程项目使用高压雾化设备的经验总结了相关建议,以期为实际生产提供参考。     

Regulatory role of l-proline in fetal pig growth and intestinal epithelial cell proliferation

l-proline (Pro) is a precursor of ornithine, which is converted into polyamines via ornithine decarboxylase (ODC). Polyamines plays a key role in the proliferation of intestinal epithelial cells. The study investigated the effect of Pro on polyamine metabolism and cell proliferation on porcine enterocytes in vivo and in vitro. Twenty-four Huanjiang mini-pigs were randomly assigned into 1 of 3 groups and fed a basal diet that contained 0.77% alanine (Ala, iso-nitrogenous control), 1% Pro or 1% Pro + 0.0167% α-difluoromethylornithine (DFMO) from d 15 to 70 of gestation. The fetal body weight and number of fetuses per litter were determined, and the small and large intestines were obtained on d 70 ± 1.78 of gestation. The in vitro study was performed in intestinal porcine epithelial (IPEC-J2) cells cultured in Dulbecco''s modified Eagle medium-high glucose (DMEM-H) containing 0 μmol/L Pro, 400 μmol/L Pro, or 400 μmol/L Pro + 10 mmol/L DFMO for 4 d. The results showed that maternal dietary supplementation with 1% Pro increased fetal weight; the protein and DNA concentrations of the fetal small intestine; and mRNA levels for potassium voltage-gated channel, shaker-related subfamily, member 1 (Kv1.1) in the fetal small and large intestines (P < 0.05). Supplementing Pro to either gilts or IPEC-J2 cells increased ODC protein abundances and polyamine concentrations in the fetal intestines and IPEC-J2 cells (P < 0.05). In comparison with the Pro group, the combined administration of Pro and DFMO reduced the expression of ODC protein and spermine concentration in the fetal intestine, as well as the concentrations of putrescine, spermidine and spermine in IPEC-J2 cells (P < 0.05). Meanwhile, the percentage of cells in the S-phase and the mRNA levels of proto-oncogenes c-fos and c-myc were increased in response to Pro supplementation, whereas depletion of cellular polyamines with DFMO increased tumor protein p53 (p53) mRNA levels (P < 0.05). Taken together, dietary supplementation with Pro improved fetal pig growth and intestinal epithelial cell proliferation via enhancing polyamine synthesis.     

Cryptic species and population genetic structure of Plasmopara viticola in São Paulo State,Brazil

Downy mildew (Plasmopara viticola) is one of the most important diseases in grape-growing areas worldwide, including Brazil. To examine pathogen population biology and structure, P. viticola was sampled during the 2015/16 growing season from 516 lesions on nine grape cultivars in 11 locations in subtropical areas of São Paulo State, Brazil. For identification of cryptic species, a subsample of 130 isolates was subjected to cleaved amplified polymorphic sequence (CAPS) analysis, and for 91 of these isolates the ITS1 region was sequenced. These analyses suggest that the population of P. viticola in São Paulo State consists of a single cryptic species, P. viticola clade aestivalis. Seven microsatellite markers were used to determine the genetic structure of all 516 P. viticola isolates, identifying 23 alleles and 55 multilocus genotypes (MLGs). Among these MLGs, 34.5% were clonal and represented 93% of the isolates sampled. Four dominant genotypes were present in at least five different locations, corresponding to 65.7% of the isolates sampled. Genotypic diversity (Ĝ = 0.21–0.89) and clonal fraction (0.58–0.96) varied among locations (populations). Most populations showed significant deviation from Hardy–Weinberg expectations; in addition, excess of heterozygosity was verified for many loci. However, principal coordinate analysis revealed no clusters among locations and no significant isolation by distance was found, suggesting high levels of migration. The results indicate that downy mildew epidemics result from multiple clonal infections caused by a few genotypes of P. viticola, and reproduction of P. viticola in São Paulo State is predominantly asexual.     

Tanshinone ⅡA induces apoptosis via JNK signaling pathway in human osteosarcoma HOS cells

AIM: To explore the effect of tanshinone ⅡA on human osteosarcoma HOS cells and the underlying mechanism.METHODS: The cell viability and the appropriate dose of tanshinone ⅡA were determined by CCK-8 assay. Colony formation assay and Transwell assay were used to investigate the proliferation and migration abilities of the HOS cells treated with tanshinone ⅡA. The apoptosis of the HOS cells was monitored by Hoechst 33258 staining, transmission electron microscopy and flow cytometry. The protein levels of apoptosis-related molecules and JNK signaling-associated proteins were determined by Western blot. Meanwhile, a JNK inhibitor was added for confirming the relationship between the pathway and apoptosis mentioned above.RESULTS: Tanshinone ⅡA inhibited both HOS cell proliferation and migration in a dose-and time-dependent manner. Exposure of the HOS cells to tanshinone ⅡA resulted in the activation of apoptosis. Tanshinone ⅡA treatment increased the protein levels of cleaved caspase-3, Bax and JNK signaling-associated proteins, and decreased the protein level of Bcl-2, which were reversed by JNK inhibitor SP600125. Moreover, the result of CCK-8 assay revealed that tanshinone ⅡA-induced cell death was alleviated by JNK inhibitor.CONCLUSION: Tanshinone ⅡA induces cell growth inhibition and the activation of apoptosis via JNK signaling pathway in human osteosarcoma HOS cells.