初生

Co-culture with Haloxylon ammodendron, the primary haustorium conglutinate with young roots of the host (0.1 mm), pass through the host's epidermis and cortex, then connect with the vascular bundle and transform into secondary haustorium, shaped by fundamental tissues of differentiation and development.

肉苁蓉与寄主梭梭共培养，其初生吸器主动与寄主幼根（0.1mm左右）黏连，穿过寄主根表皮和皮层后与维管束连通形成次生吸器，肉苁蓉植物体分化、发育的基本组织形成。

After refinement a great deal of primary iron phases appear and most of them are hexagonal.

用六氯乙烷精炼后，合金的组织中开始出现大量六角形的初生相。

The anatomical study deepens the knowledge of G-type conducting cells: 1 It proves the theory of two depositional process for secondary wall (Bierhorst, 1960): the discontinuous cellulose layer is laid down before the continuous lignified layer; the former layer is prone to be broken down, while the latter is highly decay-resistant; 2 It suggests that the cellulose primary and secondary walls of tracheids are not perforated. Instead of longitudinal pits (Li, 1992), the lignified tracheid secondary wall of Hsüa possesses irregular simple perforations; 3 In Hsüa reflexa and Huia gracilis, the perforation casts may represent the thickness of lignified secondary wall; 4 The wall structure of G-type tracheid is diversified. At the genus level, the secondary wall structure differs in the distribution, internal shape and structure of the perforations; 5 Perforations of some G-type tracheids combine the characters of S-type tracheids in their distribution, density and diameter.

解剖学的研究加深了对G-型输水管胞的认识 1）验证了管胞次生壁分两个阶段形成的理论（Bierhorst，1960），即先后形成不连续的纤维质层和连续的木质化层，前者易被分解，后者抗侵蚀性强；2）证明管胞纤维质的初生壁和次生壁不具穿孔，Hsüa管胞的木质化次生壁具有不规则的简单穿孔，而不是纵列的纹孔（Li，1992）；3）Hsüa reflexa和Huia gracilis的穿孔铸体可代表木质化次生壁的厚度；4）G-型管胞壁层结构具多样性，植物属一级的分异主要表现在次生壁穿孔的分布、孔腔形状和结构的不同；5）某些G-型管胞的穿孔在其分布、密度和孔径方面可兼有S-型管胞的特征。

In the fin219-null mutant background, GUS staining can be detected in the hydathode of cotyledons, and the guard cells around hydathodes. GUS staining are also found in the base of trichomes, hypocotyls and roots. In contrast, in the phyA mutant background, GUS-FIN219 was not expressed in the hypocotyls.

结果发现转殖在fin219-null突变株背景下，FIN219会特别表现在植株叶缘出水孔与附近的保卫细胞及毛茸基部、初生叶、下胚轴、根部等处，然而在phyA缺失的时候植株幼苗的FIN219则不会在下胚轴表现。

The process and mechanism of primary silicon growth in the Al-Si hypereutectic melt were studied by quench interrupting.

摘 要：利用等温液淬的方法，研究了Al-18%Si过共晶合金熔体中初生硅的生长行为及机制。

The experiment results showed that segregation of the primary silicon crystal in hypereutectic Al-18Si alloys was remarkable under a high magnetic field.

实验表明，在稳恒强磁场作用下，过共晶Al-18Si合金中的初生Si发生显著偏聚。

Hemolytic icterus occurs in the neonate of the horse and swine.

溶血性黄疸发生于马和猪的初生幼畜。

With a cavitating model established for N-S equations from cavitation theory, cavitation evolution on the surface of a hydrofoil is developed: incipience of cavity, cavity growing, reentrant flow appearing, cavity retracting, shedding and smaller broken cavities moving downwards with the main flow.

根据空化流原理，建立了基于N-S方程求解的空化模型，利用这个模型计算了空化在翼型表面的演化过程：初生、长大、形成回注水流、空穴回缩、减小、脱落，以及小空泡随主流向下游运动的现象。

In chapter 4, the experimentation of incipient cavitation in a transparent jet pump has been done and the data is computed.

第四章对透明射流泵的初生空化作了试验观测和数据计算研究。

Though covered in a coat of thick, soft, brown feathers, a juvenile king penguin must wait to enter the water until the age of ten months, when its first set of waterproof, adult feathers begins to grow in.

尽管被覆盖在一件厚的外套，柔软的，棕色的羽毛，一只初生的国王企鹅必须等待到10月的年龄才能进入水中，当它的第一次设置防水材料，成熟的羽毛开始增加。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。