lake effect

lake effect的基本解释

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湖泊效应

lake effect所属的单词分类

Weather / 天气 [276]

wind shear  ·  weather satellite  ·  tropical storm  ·  tropical disturbance  ·  tropical depression  ·  supercell  ·  snow level  ·  snow flurry  ·  rain shadow  ·  prevailing wind

Winter / 冬天 [151]

snow shovel  ·  lake effect  ·  ice skates  ·  ice dam  ·  bitter cold  ·  wood stove  ·  nor'easter  ·  ice scraper  ·  freezing rain  ·  black ice

与lake effect相关的网络例句 [注：此内容来源于网络，仅供参考]

The results in these three regions have been given that (1) Ephedra, as dry and desert vegetation, the average percents are 7.7 in Yang Lake, 4.2 in Kunlun Rive, 7.5 in Doucuo Lake, and the datum in Yang Lake is higher than others;(2) Gramineae, as humid vegetation, the average percents are 1.2 in Yang Lake, 4.9 in Kunlun Rive, 12.0 in Kuhai Lake, increasing gradually from west to east;(3) Artemisia, as humid vegetation, the average percents are 22.2 in Yang Lake, 43.6 in Kunlun Rive, 48.8 in Kuhai Lake, increasing gradually from west to east, too;(4) Chenopodiaceae, as dry vegetation, the average percents are 52.1 in Yang Lake, 42.4 in Kunlun Rive, 11.5 in Kuhai Lake, however, decreasing gradually from west to east;(5) Artemisia/Chenopodiaceae ,the average data, as environmental changing index, are 0.45 in Yang Lake, 1.23 in Kuniun Rive, 5.59 in Kuhai Lake, increasing gradually from west to east, and there is higher data scope during 3.0~4.3 ka BP in these two lake sediment profiles, then decreasing;(6) Ephedra/Artemisia, data are all increased but the amplitude is different, such as 0.45 in Yang Lake, 0.34 in Kunlun Rive, 0.28 in Kuhai Lake, decreasing gradually from west to east.

代表气候湿润的禾本科花粉平均百分含量，三个地区分别为：1.2%、4.9%、12.0%，从西向东数值逐渐升高。③代表气候湿润的蒿属花粉平均百分含量，三个地区分别为：22.2%，43.6%，48.8%，从西向东数值逐渐升高。④代表气候干旱的草科花粉平均百分含量，三个地区分别为：52.1%，42.4%，11.5%，从西向东数值逐渐降低。⑤依据蒿属、藜科花粉百分含量，计算出环境变化指标，蒿属／藜科值，三个地区的平均值分别为：0.45，1.23，5.59，从西向东比值逐渐升高，⑥麻黄属／蒿属值，在全新世晚期，三个地区都呈上升趋势，但幅度存在差异，分别为：0.45，0.34，0.28，从西向东数值逐渐降低。

The stable clones are further identified by RT-PCR and Western blot; 6 MTT assay is used to investigate the effect of ZNRD1 on the cell growth of cells (AGS, SGC7901, MKN28, NIH3T3, GES-1); 7 Soft agar assay is used to investigate the effect of ZNRD1 on the clonality of cells (AGS, MKN28); 8 Nude mice assay is used to investigate the effect of ZNRD1 on the cell growth of gastric cancer cells (AGS, MKN28); 9 Flow cytometry is used to investigate the effect of ZNRD1 on the cell cycle distribution of cells (AGS, MKN28, NIH3T3, GES-1); 10 Flow cytometry is used to investigate the effect of ZNRD1 on the cell apoptosis of cells (AGS, MKN28, NIH3T3); 11 MTT assay is used to investigate the effect of ZNRD1 on the drug sensitivity of cancer cells (SGC7901, SGC7901/VCR, HL-60, HL-60/VCR) in vitro; 12 SRCA is used to investigate the effect of ZNRD1 on the drug sensitivity of gastric cancer cells (SGC7901, SGC7901/VCR) in vivo; 13 Flow cytometry is used to investigate the effect of ZNRD1 on adriamycin accumulation of cancer cells (SGC7901, SGC7901/VCR, HL-60, HL-60/VCR); 14 Transmission electron microscope is used to investigate the effect of ZNRD1 on the sensitivity of SGC7901 cells towards drug-induced apoptosis; 15 Flow cytometry and DNA ladder assay are used to investigate the effect of ZNRD1 on the sensitivity of cells (SGC7901, SGC7901/VCR, HL-60/VCR) towards drug-induced apoptosis; 16 Microarray is used to investigate the profiling of ZNRD1-responsive genes in gastric cancer cells (AGS, MKN28, SGC7901, SGC7901/VCR); 17 RT-PCR and Western blot are used to identify the results of microarray; 18 Reporter gene assay is used to investigate the effect of ZNRD1 on the transcriptional activity of cyclin D1; 19 Reporter gene assay is used to investigate the effect of ZNRD1 on the transcriptional activity of MDR1; 20 Kinase assay is used to investigate the effect of ZNRD1 on the activity of cyclin E-CDK2 kinase; 21 The antisensenucleic acids of p21 is used to inhibit the expression of p21, and flow cytometry is used to investigate the effect of p21 on ZNRD1-induced cell cycle arrest in gastric cancer cells; 22 The antisensenucleic acids of p27 is used to inhibit the expression of p27, and flow cytometry is used to investigate the effect of p27 on ZNRD1-induced cell cycle arrest in gastric cancer cells; 23 Liposome is used to up-regulate the expression of Skp2, and flow cytometry is used to investigate the effect of Skp2 on ZNRD1-induced cell cycle arrest in gastric cancer cells; 24 Western blot is used to investigate the effect of ZNRD1 on the stability of Skp2 and p27 in gastric cancer cells; 25 MVD assay is used to investigate the effect of ZNRD1 on the angiopoietic activity of gastric cancer cells; 26 ELISA is used to investigate the effect of ZNRD1 on the expression of VEGF165 in gastric cancer cells; 27 The roles of DARPP-32 in MDR of gastric cancer cells are investigated using gene transfection, MTT assay, SRCA, flow cytometry and DNA ladder assay.

应用杂交瘤技术制备ZNRD1的首个单克隆抗体；2）利用RT-PCR、Western blot和免疫组化检测ZNRD1在胃癌组织、胃炎组织、正常胃上皮组织、胃癌细胞和正常胃组织上皮细胞中的表达；3）构建ZNRD1的小干扰RNA载体，并测序鉴定；4）利用脂质体将ZNRD1的真核表达载体及其空载体转染胃癌细胞（AGS、SGC7901、MKN28）和小鼠成纤维细胞（NIH3T3），G418筛选后进行鉴定；5）利用脂质体将ZNRD1的小干扰RNA载体及其空载体转染药敏胃癌细胞（SGC7901）、正常胃组织上皮细胞（GES-1）、对长春新碱耐药的胃癌细胞（SGC7901/VCR）、药敏白血病细胞（HL-60）、对长春新碱耐药的白血病细胞（HL-60/VCR），G418筛选后进行鉴定；6）利用MTT实验检测ZNRD1高/低表达对细胞（AGS、SGC7901、MKN28、NIH3T3、GES-1）生长的影响；7）通过软琼脂克隆形成实验检测上调ZNRD1对AGS、MKN28细胞克隆形成能力的影响；8）通过裸鼠成瘤实验检测上调ZNRD1对AGS、MKN28细胞体内成瘤性的影响；9）通过流式细胞仪分析ZNRD1高/低表达对细胞（AGS、MKN28、NIH3T3、GES-1）的细胞周期的影响；10）通过流式细胞仪分析上调ZNRD1对细胞（AGS、MKN28、NIH3T3）的凋亡的影响；11）通过MTT实验检测ZNRD1高/低表达对细胞（SGC7901、SGC7901/VCR、HL-60、HL-60/VCR）体外药物敏感性的影响；12）通过肾包膜下移植法检测ZNRD1高/低表达对细胞（SGC7901、SGC7901/VCR）体内药物敏感性的影响；13）通过流式细胞仪分析ZNRD1高/低表达对细胞（SGC7901、SGC7901/VCR、HL-60、HL-60/VCR）内阿霉素蓄积和泵出的影响；14）通过透射电镜检测上调ZNRD1对SGC7901细胞凋亡敏感性的影响；15）通过流式细胞仪和DNA梯度试验检测ZNRD1高/低表达对细胞（SGC7901、SGC7901/VCR、HL-60）凋亡敏感性的影响；16）通过基因芯片检测ZNRD1高/低表达对胃癌细胞内基因表达谱的影响；17）利用RT-PCR、Western blot对基因芯片的结果进行鉴定；18）利用报告基因实验检测ZNRD1对cyclin D1的启动子活性的调节作用；19）利用报告基因实验检测ZNRD1高/低表达对MDR1的启动子活性的调节作用；20）利用激酶试验检测ZNRD1对cyclin E-CDK2 激酶活力的影响；21）利用反义核酸技术抑制p21的表达；通过流式细胞仪检测抑制p21对ZNRD1介导的细胞周期阻滞的影响；22）利用反义核酸技术抑制p27的表达；通过流式细胞仪检测抑制p27对ZNRD1介导的细胞周期阻滞的影响；23）利用脂质体转染法上调Skp2的表达；通过流式细胞仪检测上调Skp2对ZNRD1介导的细胞周期阻滞的影响；24）利用Western blot检测ZNRD1对p27和Skp2的蛋白稳定性的影响；25）利用微血管密度实验检测ZNRD1对AGS、MKN28细胞裸鼠移植瘤微血管形成的影响；26）利用ELISA检测ZNRD1对AGS、MKN28细胞培养上清和移植瘤匀浆中VEGF165含量的影响；27）利用脂质体转染法、MTT实验、肾包膜下移植法、流式细胞仪和DNA梯度试验检测新耐药相关分子DARPP-32对细胞（SGC7901、SGC7901/VCR、对阿霉素耐药的胃癌细胞SGC7901/ADR）多药耐药表型的影响；利用脂质体转染法和MTT实验检测下调ZNRD1对DARPP-32介导的胃癌多药耐药的调控作用。

Three main methods with lacustrine carbonates have been used to reconstruct the lake water palaeo-temperature at present. First, the technique of isotopic geological thermometer, since being put forward to reconstruct sea-water paleo-temperature, was subsequently introduced into lacustrine carbonate sediments for constructing lake-water based upon the function relationship between lake-water temperature and the oxygen isotopic compositions of lacustrine carbonate and lake-water. Second, paleo-temperature of the lake-water can be reconstructed by determining Mg/Ca values of the lacustrine ostracode shells. And third, paleo-temperature of the lake-water can be reconstructed based upon the statistic model between the oxygen isotopic composition of lacustrine carbonate and the Lake-water temperature by testing the modem hydrogeological parameters and some relevant isotopic data of the lake basin.

目前利用湖泊碳酸盐对湖泊古水温进行重建主要有三种方式，一是运用同位素地质温度计原理，利用水温与湖泊碳酸盐氧同位素值和湖水氧同位素值三者之间的函数关系，对湖泊古水温做定量研究；二是通过测定介壳[Mg(上标 2+)]/[Ca(上标 2+)]进而重建古水温；三是通过测定湖泊流域范围内现代水文气象参数及一些相关的同位素资料直接建立起湖泊自生碳酸盐氧同位素值与温度间的统计模型。

与lake effect相关的网络解释 [注：此内容来源于网络，仅供参考]

Huron, Lake：休伦湖

它们按大小分别为苏必利尔湖(Superior Lake), 休伦湖 (Huron Lake),密歇根湖 (Michigan Lake),伊利湖 (Erie Lake)和安大略湖(Ontrio ... ,注入大西洋. 尼亚加拉河 ... ,水量丰富的尼亚加拉河...

put into effect /bring into effect /carry into effect：使 生效

in effect 实际上,简直是 | put into effect /bring into effect /carry into effect 使 生效 | without effect 没有作用(作状语)

come into effect：生效,实施in effect 有效,实际上

put into effect 实行,生效 | come into effect 生效,实施in effect 有效,实际上 | take effect 生效,起作用