苏南丘陵区秋播苜蓿适用伴生作物筛选试验   总被引：3，自引：0，他引：3  

戚志强胡跃高  曾昭海傅反生 储国良 《中国草地》2005,27(5):22-28

为解决苏南丘陵区苜蓿苗期的杂草问题,从保护播种入手,在多年生黑麦草、一年生黑麦草、黑麦、小黑麦四种作物共五个品种中寻找适宜的伴生作物.通过对产量、株高、杂草率等多个指标测定分析,筛选出中新830小黑麦、赣选一号黑麦草适于用作苜蓿播种的伴生作物,同时获得两个苜蓿存活率最高的处理：苜蓿（15kg/hm^2）＋中新830小黑麦（150kg/hm^2）撒播及苜蓿（18 kg/hm^2）＋中新830小黑麦（250kg/hm^2）30cm条播.试验还表明撒播方式下,苜蓿播量与其竞争力不成正比。  相似文献   

类鼻疽的研究进展     

李志敏  肖啸  项勋  夏春香 《家畜生态》2005,(5)

本文就类鼻疽(melioidosis)的流行病学,诊断方法,免疫机理,发病机理及治疗方法 进行了综述。为重视该病的研究提出了建议。  相似文献   

阜康绿洲土壤盐渍化特征及其与肥力的相关性分析   总被引：9，自引：0，他引：9  

顾峰雪  张远东  刘永强  初雨  潘晓玲 《干旱区资源与环境》2003,17(2):78-82

本文以电导、可溶性总盐含量和pH作为指标,将阜康绿洲的盐渍化类型划分为9种,其中以强盐渍土和盐土为主,在纬度梯度上从南至北,即从洪积扇下部到沙漠按照中盐渍土-强盐渍土-盐土-强盐渍土-盐土-非盐渍土的顺序依次分布。而土壤含水率却是从洪积下部至扇缘溢出带逐渐升高,在细土平原地区差异较大,在沙漠中又迅速降低。通过土壤剖面中有机质、全量N、P、K和速效N、P、K的分析,结果表明阜康荒漠自然状态下土壤肥力很低,各养分含量在空间上呈现规律性的变化,在纬度梯度上逐渐升高又在沙漠中降低。通过水盐与土壤肥力的相关性分析,结果表明:有机质、全N、P和速P与含水率、电导、总盐均具有显著和极显著正相关,而与pH成负相关,但相关性不显著。由于盐生植物的多样性,在盐渍土和盐土土壤肥力并无显著降低,只是土壤溶液的高盐浓度限制了植物对养分的吸收,因此防止和治理土壤盐渍化是发挥土地生产潜力的重要手段。  相似文献   

Changes of urinary albumin and N-acetyl-beta-glucosaminidase in high altitude polycythemia at different altitudes and its mechanism     

XI Ai-qi  CHU Yi-de 《园艺学报》2003,19(6):815-817

AIM:To study the changes of excretive amount of albumin(ALB), N-acetyl-beta-D-glucosaminidase(NAG) in patients with high altitude polycythemia(HAPC) at different altitude and its mechanism.METHODS:Urinary ALB, NAG, activity of red blood cell superoxide dismutase(RBC-SOD), malonyldialdehyde(MDA) and erythrocyte filtration index(EFI) of 231 healthy subjects and 86 patients with HAPC at different altitude were detected.RESULTS:Excretive amount of urinary ALB, NAG, and plasma MDA, EFI were higher, and RBC-SOD was lower in patients with HAPC than those in healthy subjects, the changes were significantly obvious, with increasing altitude. Urinary ALB and NAG were negatively correlates to EFI, and no correlated to the content of MDA and RBC-SOD.CONCLUSIONS:EFI exertes an independent influence on urinary ALB and NAG. The decrease in erythrocyte deformability caused by the increase of peroxidation of lipids might participate in the pathogenesis and progress of the increase of excretive amount of ALB and NAG in HAPC.  相似文献   

Selection and amplification of the liver stem cell subset from rat bone marrow cells with a medium containing cholestatic serum in vitro     

CAI Yun-feng  MIN Jun  FANG Tian-ling  CHU Zhong-hua  DENG Xiao-geng  HE Jing-song  CHEN Ji-sheng 《园艺学报》2003,19(8):1029-1033

AIM: To explore the feasibility of direct separat and selective enlargement of the bone marrow-derived liver stem cells (BDLSC) from bone marrow cells with a culture system containing cholestatic serum in vitro. METHODS: Bone marrow cells of rats were cultured with selective media containing 2%, 5%, 7% and 10% cholestatic rat serum, respectively. The BDLSC were then induced to proliferate with the addition of hepatocyte growth factor (HGF) on the firth day. BDLSC were characterized using immunocytochemistry and RT-PCR for lineage markers, glycogen staining and urea synthetic assay for functions 2 weeks later. RESULTS: Bone marrow cells were unble to form colony in the presence of 2% cholestatic serum and apopotosis appeared gradually in 7% or 10% cholestatic serum. The BDLSC survived in the medium containing 5% cholestatic serum while the other types of cells did not. The survival cells proliferated with a high speed during the second week and then formed hepatocyte-like colony-forming units (H-CFU). Cells in the H-CFU expressed the characteristic proteins of fetal hepatocytes. Furthermore, they had glycogen storage and urea synthesis functions, two of the critical features of hepatocytes. CONCLUSION: The selective micro-environment effectively selected BDLSC from the bone marrow cell, and will be a new way to provide an abundant source of donor hepatocytes for clinical cell therapy.  相似文献   

Effect of mutant β-catenin gene on the proliferation of hepatocytes     

SHANG Xian-zhang  MIN Jun  CHU Zhong-hua  CHEN Ji-sheng 《园艺学报》2003,19(12):1601-1605

AIM:The β-catenin is a key molecule in the Wnt signal pathway, which plays a critical role in normal development and tumorigenesis. However, the mechanisms of the β-catenin on the cell growth control are still not completely defined. The aim of this study was to test the hypothesis that the mutant β-catenin may regulate the hepatocyte proliferation. METHODS: The immortalized murine hepatocyte cell line, AML12, was used for this study. A plasmid that contain mutant β-catenin S33Y was transfected into the AML12 cells and a stable cell line AML12S33Y was established. The cell growth property of this cell line and the parental cell were compared by flow cytometry analysis and direct cell count. The cells were also tested for the ability to form soft agar colonies, and the ability to form tumors in the severe immune deficient mice (SCID). RESULTS:1. The mutant β-catenin containing cell line AML12S33Y has higher proliferating index compared with the parental AML12 cells (P<0.01), suggesting that mutant β-catenin promotes cell growth. 2. The mutant β-catenin cells formed small colonies in soft agar after 4 weeks of culture, but did not generate tumor in SCID mice. CONCLUSION:The mutant β-catenin promotes liver cell growth.  相似文献   

Effect of antifibrotic herb serum on rat hepatic stellate cell proliferation and collagen synthesis     

LING Yun-biao  XU Rui-yun  QIU Wan-shou  CHU Zhong-hua  YANG Hong-zhi  TAN Zhi  OU Qing-jia 《园艺学报》2003,19(12):1649-1652

AIM: To investigate the effect of Chinese herbs, Ganxianfang(GXF), on rat hepatic stellate cells (HSC) proliferation and collagen synthesis. METHODS: Two types of herb serum, portal venous serum and circumferential venous serum, were prepared from rats infused intragastrically with 16, 8, 4 times adult dose of GXF decoction. HSC isolated from rat liver were processed with the above sera in vitro. Then we mensurated the radioactivity of HSC admixed with [[³H]H]proline and [[³H]H]thymine to judge the effect on proliferation and collagen synthesis of HSC. RESULTS: Both two types of serum collected 0.5, 1, 2 h after intragastrical infusion inhibited HSC proliferation (P＜0.05), and the serum collected 1 h after intragastrical infusion had the strongest effect (P＜0.05). Portal serum decreasea collagen synthesis (P＜0.05), but circumferential serum had no effect (P＞0.05). CONCLUSION: Inhibition of HSC proliferation and decrease of collagen synthesis may contribute to the GXF antifibrotic action.  相似文献   

莫莫格湿地干-湿界面优势植物种群动态分析   总被引：1，自引：0，他引：1  

田迅  卜兆君 《四川草原》2004,(11)

莫莫格湿地从高河漫滩底端到顶端选取有代表性的植物群落片断作为固定观测样带,并设置6个观测样方,生长季5月、7月、9月3次观测结果表明,小叶章优势种群5月份密度最高达1154-1594株/平方米,7月种群数量下降,9月有所升高;踏头苔草优势种群5-7月份密度在3 414-7 193株/平方米,9月份种群数量大幅度下降;土壤相对含水量低地段小叶章种群相对优势度大,土壤相对含水量高地段踏头苔草种群相对优势度大,局部地段生长季内有相对优势度相互替代过程,莫莫格湿地干-湿界面上小叶章和踏头苔草两个种群可以共存。  相似文献   

Effect of EGFP gene transfection on the cell cycle distribution of primary cultured human chondrocytes     

JIANG Xun  ZENG Yao-ying  HE Xian-hui  XU Li-hui  DI Jing-fang  FENG Zheng  ZHAO Jing-xian  WANG Qing  WANG Tong  SHI Jian-bo 《园艺学报》2004,20(6):924-928

AIM: To investigate the effect of enhanced green fluorescence protein (EGFP) gene transfection on the cell cycle distribution of primary cultured human chondrocytes in order to establish a tracking method of cultured human nasoseptal chondrocytes. METHODS: pEGFP-N1 plasmid was amplified in E.coli, and purified by high purity kit. Primary cultured human chondrocytes,which were initially obtained from the nasoseptal cartilage, were cultured in vitro and transferred with pEGFP-N1 by means of electroporation with Amaxa nucleofector device. Transfering process and transient expression were evaluated by laser scanning confocal microscope (LSCM), the transfer efficiency and the cell cycle distribution were evaluated by flow cytometry. RESULTS: There was significant expression of EGFP at 24 h after transferring. The transfection efficiency of pEGFP-N1 into primary cultured human chondrocytes reached 35.37％ at 48 h. It didn't affect the process of cell adherance and had no effect on the cell cycle distribution. CONCLUSION: Primary cultured human chondrocytes, which were transfected with pEGFP, are alive in vitro, and the transferring process doesn't affect the cell cycle distribution. These results suggest that pEGFP-N1 is an ideal transient expression vector for primary cultured human chondrocytes and it might be a well tracer in construction tissue engineered cartilage.  相似文献   

Bone marrow mesenchymal stem cells are induced to differentiate into cardiomyocytes by hepatocyte growth factor in vitro     

FANG Tian-ling  MIN Jun  DENG Xiao-geng  QIAN Shi-kun  CHU Zhong-hua  CHEN Ya-jin  SHAO Jing  WEI Jing  CHEN Ji-sheng 《园艺学报》2004,20(7):1167-1170

AIM: To explore a new method of hepatocyte growth factor (HGF) inducing bone marrow mesenchymal stem cells (MSC) to differentiate into cardiomyocytes. METHODS: Bone marrow MSC was cultured with DMEM media (10% fetal calf serum) 4-6 passages, and induced by HGF (10 μg/L) for 30 d. Automatical beating of the differentiated cells was observed daily with transverse microscopy, or under condition of 0.1% isoproterenol or cal-cium-deprived incubation. Specific cardiac myosin in the cells was indentified by immunochemistry. RESULTS: At 14-20 d of differentiation, bone marrow mesenchymal stem cells formed clones, in 10%-50% of which spontaneous beating cell-mass had come to continuously exist. Isoproterenol increased the beating rate and calcium-deprived media inhibited the beating. The cells were identified to be cardiomyocytes by expression of cardiac myosin heavy chain. CONCLUSION: HGF may induce bone marrow mesenchymal stem cells into cardiomyocytes with high efficiency, but the differentiating pathway of stem cells remains to be further studied.  相似文献