Elongated caudex branches; a shoot arising from the base of a stem or from the rhizome.

根出條 Sobol 發(fā)自莖基的長枝條日本视频网址；從莖的基部或根狀莖上長出的枝條日韩爱色成人片在线观看视频网站。

You will come in May between June, between choice section shorter give birth to half lignification branch in those days, from base the ministry cuts dirty to insert spic, topmost reservation comes 3 pieces 5 flocculus, if branch is too long, yi Ke bite off carries a tip on the head, cuttage medium can use humus soil of orchid mud, high mountain, vermiculite, pearlite or Huang Xin earth to wait, thick about 15 centimeters reach 20 centimeters, the catchment layer that lower berth reachs 8 centimeters 7 centimeters; medium after in season is wet, in will inserting spic to insert matrix, deepness of the be buried that insert spic makes an appointment with the 1/2 that grows for spic, a few cuttage also can choose the family full-dress medium generation makes big flowerpot cuttage seedbed.

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They have distinctive compositions, and display the compositional trends: from Mg and Ca-enrichment towards Fe-enrichment from big phenocryst—the core of small phenocryst—the rim of small phenocryst and microcrystals, typical characterisitc of tholeiite series.

這三種類型的輝石在成分上有明顯的差異亚洲激情国产一区精品，從大斑晶輝石—小斑晶輝石核部—小斑晶輝石邊部和基質(zhì)輝石，成分由富鎂丰满熟女456视频、鈣向富鐵方向演化人人干人人操在线，顯示出拉斑玄武系列的特點。

The breed of gilt-edged wind pear basically is to use cuttage method; It has stronger cent to give birth to ability, after be being spent every year, chairman of phyllome radical department gives new shoot, in those days autumn can cut next enter growing in pearlite and vermiculite compound matrix, wait for rooted hind go up again basin conserve.

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The spermatozoa are embeded in a extracellalar matrix composed of high dense fibrils matrix and flocculent and concentric vesicles similar to that in the primary spermatophore layer, but the later lack of spermotozoa. The flocculent and concentric vesicles are often seen to release their contents around the main body of spermatozoa. The spermatozoa may absorb the contents to form vesicular zone and membrane zone in sperm nucleu. The secondary spermatophore layer is distinctly subdivided into inner region and outer region. The loose outer region consists of canaliculated reticulum and large flocculent vesicles.

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Corolla white, yellow, or purple-red, 2-lipped; tube dilated in front near base, long exserted, not hairy annulate inside; upper lip short, straight, margin entire or emarginate; lower lip longer, subpatent, 3-lobed; middle lobe largest, emarginate, margin undulate to dentate.

花冠白色一级大香一级大香香蕉，黃自拍偷拍网页，或紫色紅色，二唇形欧美黄色一级网站；在前面擴大的筒部近基部玖玖相交视频，長，不有毛有環(huán)在里面先峰资原吧；上唇短欧美性爱影视一区二区三区，直，邊緣全緣或微缺黄片儿小视频；下唇長18禁看插她，subpatent，3淺裂自拍偷拍毛片；大黄色网操B人人操老女人B网，微缺的中部裂片，邊緣波狀對具牙齒QVOD经典激情视频图片小说。

Stamens inserted on corolla, included to exserted, equal in number to corolla lobes and alternating with them or sometimes fewer; filaments free, much shorter to much longer than anthers; anthers basifixed, 2--4-locular, dehiscing introrsely or extrorsely by longitudinal slits, base slightly to deeply parted.

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Corolla zygomorphic, ventricose funnelform, tube narrow at base, throat wide; limb oblique, ca. 2-lipped, upper lip 2-lobed or entire, lower lip 3-lobed with middle lobe larger.

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It"s vegetal mycelia were colorless, smooth, 1.2μm～3.0μm crude, manyconidiogenous cells born on vegetal mycelia, sometimes as many as a dozen,a very small number were single. The base of conidiogenous cell wasenlarged and many of them were bottle-shaped or spherical. The upper ofconidiogenous cell extended into a conidiogenous axis of 1μm wide and 14μm length which was the knee-bending ("Z like bending), there were small pectinae on the axis, conidium located on the small pectina.

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The hFCECs were cultured by sticking tissues piece method that the cornea were divided into the limbus and central tissue piece and digestive method,respectively.For digestive method,the digestive juice of 5mg/ml DispaseⅡ+0.25%trypsin was chosed.D/F12 with 10%fetal bovine serum and 100 U/ml penicillin and streptomycin were used in this study,the culture condition was 37℃and 5%CO2,and culture medium changed every three days2国产欧美色,一区二区三区、Passage of hFCECsAfter more than 80%confluenced,cells from corneal limbus hFCECs were digested for 5-15min with different concentrations of trypsin/EDTA at 37℃,and then passaged at a ratio of 1:2.The cells were subcultured on empty plates,mouse 3T3 fibroblast feeder layer,fetal corneal stromal cell feeder l ayer or HTK feeder layer respectively.And D/F12, mouse 3T3 fibroblast conditioned medium,fetal corneal stromal cells conditioned medium or HTK conditioned medium with 10%FBS and 100 U/ml penicillin and streptomycin were used respectively as the culture medium.And the culture medium were changed every three days as well.

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