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overall pattern     
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  总体格局
     It is to give a comment on the overall pattern of LU Xun's confrontational thought studies from1913 to 2003 in terms of ideological trend school, and differentiate and analyze the views of every ideological trend schools.
     文章从思潮流派的角度论述从1913年到2003年间鲁迅反传统思想研究的总体格局,并对各思潮流派的观点作以辨析。
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     A“not correspondence” will be found between the Chinese literature and the western literature if we survey the Modern Chinese Literature newly by placing it into the overall pattern of thd literature of the world, which is mainly due to our lacking enough knowledge on Lu Xun's modernism.
     把中国现代文学置于世界文学总体格局中的重新审视产生的是中西文学之间的“不对应感”,这主要根源于对鲁迅的现代主义缺乏充分的认识。
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     Judged by the overall pattern of prefectural and municipal society, the prefectural and municipal colleges and universities are the influential social units and play a promoting role in training senior talented persons, social political construction, economic development, cultural conformation, reform and development of education.
     从地市社会总体格局看 ,地市高校是地市社会中具有特殊影响的社会单位 ,对地市社会高层次人才培养培训、社会政治建设、经济发展、文化整合、教育改革与发展都具有积极的推动作用
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     Though the research on preface is far from satisfactory and is limited in many ways, in regard to the overall pattern it has entered a new stage.
     虽然还存在一些不足和局限,但就其总体格局而言,则标志着唐代序文研究已经进入新的阶段。
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     UN Convention Against Corruption,the first legal document on global anti-corruption,has important and farreaching influence upon forming an overall pattern for international combat against corruption,perfecting legal system against corruption in China and developing international cooperation.
     《联合国反腐败公约》是第一项全球性反腐败法律文书,对形成国际反腐败斗争的总体格局和健全完善我国的反腐败法律制度及对外开展反腐败国际合作具有重要和深远影响。
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     Basing on the trade development theory of "Growth Triangle", this paper researchs a conflict and a pattern of the short term trade development stage of Tumen River Economic Zone through conflict analysis technique, which laies a theoritical foundation and furnishes a technical guarantee to decide the overall pattern and strategy for the trade development in Tumen River Economic Zone.
     以“成长三角”贸易发展理论为基础,采用冲突分析技术,研究了图们江经济区贸易发展近期的冲突问题,指出了图们江经济区贸易发展近期模式。 为图们江经济区贸易发展总体模式的确定和可供选择的贸易发展战略的提出奠定了理论基础,提供了技术保证
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  “overall pattern”译为未确定词的双语例句
     On the Construction of the Overall Pattern of Cultural Qualities Education
     构建全方位的文化素质教育模式
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     Since Asia's financial crisis broke out in 1997, the composite model of market risks and credit risks, the problem on quantitating operational risks and overall pattern of risks management have drawn people's more attention.
     1997年亚洲金融危机爆发以来,促使人们更加重视市场风险与信用风险的综合模型以及操作风险的量化问题,由此全面风险管理模式引起人们的重视。
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     Derived from 2D wavelet transform, the calculation of wavelet variance can reduce the four-dimensional data of wavelet coefficient to two-dimensional wavelet variance function, and quantify the contribution of the given scale to the overall pattern.
     小波方差从二维小波分析导出,小波方差可将四维的小波系数降至二维的小波方差函数,并量化所分析格局规模对整个格局的贡献。
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     The present study investigates the overall pattern of English vocabulary learning strategies by some Chinese college students of science at a common university and their specific memorization strategies employed as well as the differences in English vocabulary strategy use between some Chinese college students of science at a common university and some Chinese college students of science and humanities at a key university, a teachers university and a common university.
     本研究调查了部分中国普通高校理科生使用英语词汇学习策略的总体情况、具体的英语词汇记忆策略、普通高校理科生和重点、师范及普通三类高校综合来看的文理生在英语词汇记忆策略使用上的不同以及成功语言学习者及普通高校理科生在学习策略上的差异。
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     This study attempted to explore the overall pattern of English vocabulary learning strategies used by Chinese junior high school students and the training effects of two vocabulary learning strategies on their vocabulary acquisition.
     本研究试图了解中国中学生使用英语词汇学习策略的总体情况以及经过两种词汇学习策略的培训之后对学生词汇习得的影响。
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  overall pattern
The overall pattern of product inhibition corresponds to an ordered steady-state mechanism following the sequence SAM↓DNA↓metDNA↑SAH↑ (S-adenosyl-L-homocysteine).
      
The overall pattern of product inhibition corresponds to an ordered steady-state mechanism following the sequence SAM↓DNA↓metDNA ↑SAH↑ (S-adenosyl-L-homocysteine).
      
The O?H bonds between water molecules and Cl?H bonds in the nearest surroundings of the anions make approximately equal contributions to the overall pattern of H bonds in the water subsystem.
      
On the basis of these data, it is concluded that the modification of each structural element of the udp regulatory region (binding sites for CytR, CRP, or RNA polymerase) caused changes in the overall pattern of the promoter regulation.
      
The overall pattern of the transport voltage distribution along the disk is seriously transformed.
      
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The fossil Leporidae described in the present paper were collected from Middle Oligocene deposits at Ulantatal in Western Nei Mongol by an IVPP field team in 1978. The small collection consists of over ten specimens including upper and lower jaws, representing one species, Ordolagus teilhardi. Ordolagus teilhardi was previously known by only two broken lower jaws recovered from Middle Oligocene deposits of Shanshenggong, Nei Mongol and from the deposits of same age at Hsanda Gol, Mongolia. Newly discovered upper...

The fossil Leporidae described in the present paper were collected from Middle Oligocene deposits at Ulantatal in Western Nei Mongol by an IVPP field team in 1978. The small collection consists of over ten specimens including upper and lower jaws, representing one species, Ordolagus teilhardi. Ordolagus teilhardi was previously known by only two broken lower jaws recovered from Middle Oligocene deposits of Shanshenggong, Nei Mongol and from the deposits of same age at Hsanda Gol, Mongolia. Newly discovered upper cheek teeth show greater range of morphological diversity than was previously known fo this species. Lagomorpha Brandt, 1855 Leporidae Gray, 1821 Ordolagus Muizon, 1977 Revised diagnosis Lower jaw deep and robust. Cheek teeth hypsodont. Upper cheek teeth anteroposteriorly compressed with strongly curved crowns. There is no evidence of a hypostria, and the primitive structure on the surface may exist only in very young individuals. P~2 width greater than length, with a single anterior re?ntrant that crosses one-third of the occlusal surface, P~3 and P~4 fully molariform. M~1 is the largest upper cheek tooth. Lower cheek teeth are similar to those of Gobiolagus both in size and in morphology, differ from the latter in no or much reduced anterointernal and anteroexternal re?ntrants on P_3, nonpear-shaped trigonids with pronounced posterior projections on P_4-M_2. Obliquely setting M_3 with only one lateral groove. Ordolagus teilhardi (Burke) 1941 Material Right P_3-M_2 (V6268.1); left P_3-M_1 (V6268.2); left M_1-M_2 (V6268.3); right P_4-M_3 (V6268.4); left M_1-M_2 (V6268.5); right P_3 and trigonid of P_4 (V6268.6); left P_3-M_2 (V6268.13); right P~3-M~3 (V6268.7); right P~3-M~2 (V6268.8); left P~3-M~2 (V6268.9); left P~3-P~4 (V6268.10); right P~3-M~3 (V6268.11); right P~2-M~2 (V6268.12); right P~4-M~1. Description Horizontal ramus deep and robust, measuring 12.3 mm and 11.2 mm labially below M_2 in V6268. 13. The masseteric fossa is shallow, terminating anteriorly below M_1. One mental foramen is situated below the diastema and a second lies in front of and below P_4 in most specimens. The lower incisor in all specimens extends posteriorly along the ventrolingual side of the jaw, and terminates below M_1. Size and morphology of lower cheek teeth slightly varies among specimens. P_3 consists of two lobes: the trigonid is narrower than the talonid, and a main posteroexternal re?ntant between the trigonid and talonid spans more than one-third of the tooth. The dentine of the lobes is lingually confluent. In some specimens the trigonid appears to be divided into two sections due to the presence of less developed anterointernal and anteroexternal re?ntrants. In general, P_4, M_1 and M_2 are similar. Each consists of a trigonid and a narrower talonid that are united lingually by a bridge of enamel and dentine. Tooth size increases from P_4 to M_2. The talonid of P_4 is leaf-like, while in M_2 is nearly triangular. The posterior projection on the trigonid of P_4 is the largest of the three teeth. M_3 is preserved only in V6268.4, obliquely set posterior to the talonid of M_2. M_3 is smaller than any other cheek teeth in this species. Two columns are indicated by a narrow labial groove. The talonid on M_3 is small and circular, situated lingually behind the trigonid. This tooth is also relatively smaller than M_3 found in previously studied specimens. Cement is present between the columns on P_4 to M_2 and fills the external re?ntrants on P_3 and M_3. The anterior root of the zygomatic arch extends to the anterior surface of P~3. The upper cheek teeth are broken labially, except for P~2 and M~3. P~3-M~2 are very wide. P~2 is wider than long with a single anterior re?ntrant that crosses about one-third of the occlusal surface. The anterior portion of the tooth is divided by the re?ntrant into a big external (buccal) lobe and a smaller internal (lingual) one. The P~2 enamel is well developed lingually, but it is thin buccally. P~3, P~4, M~1 and M~2 are similar in overall pattern, demonstrating that the last two premolars are fully molariform. There is no evidence of a hypostria on p~3-M~2, and a small remnant of a crescent is present nly in younger individuals (e.g., V6268.12). Theenamel is well developed anteriorly and lingually, but it is thinner or reduced posteriorly and buccally. M~3 is much smaller than p~2, and has an elliptical occlusal surface. Comparison and discussion Burke (1941) created a new genus, Gobiolagus, including four species, G. tolmachoui (Late Eocene), G. andrewsi (Early Oligocene), G. ? major (early Oligocene), and G. ? teilhardi (Middle Oligocene). All of these taxa were based solely on lower jaws and cheek teeth from Nei Mongol and Mongolia. The last species, G. ? teilhardi, based on a broken.lower jaw, was created by Burke, comparing with the specimen, which Teilhard designated as Duplicidentes indetermines, from Shanshenggong. Burke himself doubted that this material warranted a new genus: "The generic position of Gobiolagus (?) teilhardi must remain in some doubt until better material representing the species is available, when such material is studied, the species may prove to belong to a distinct genus." (Burke, 1941). In 1968 Teilhard's specimen was reprepared by Janvier, and some previously unknown features were revealed. Muizon (1977) recognized differences between Teilhard's specimen and the types of Gobiolagus tolmachovi and G. andrewsi. Subsequently, Muizon (1977) referred Teilhard's material (ie., Gobiolagus ? teilhardi) to a new genus, Ordolagus teilhardi. The 1978 IVPP field team found a great many lagomorph specimens at Ulantatal localities in Nei Mongol. In that collection, several lower jaws and cheek teeth are similar to those of Gobiolagus in the increase in size from P_4 to M_2, leaf-like P_4 talonids placed close to the poste- rior slope of the trigonid. M_2 is the largest tooth in the lower molar series. The talonids and trigonids of P_4-M_2 are united lingually by a bridge of enamel and dentine, as described above. These specimens were originally referred to Gobiolagus. Muizon (1977), however, pointed out some important differences between Ordolagus and Gobiolagus. In the former, the cheek teeth are hypsodont, the lower jaw is deep, and M_3 is sct obliquely to the tooth row with only one furrow on the labial side. The trigonids of P_4-M_2 possess distinct posterior projections. In Gobiolagus, the cheek teeth are subhypsodont or unilaterally hypsodont, as Burke pointed out. Re?ntrants or furrows on the lower cheek teeth of Gobiolagus never extend below the alveolarmargin. M_3 is placed nearly penpendicular to the alveolar margin and has two grooves on both lingual and labial sides. There are no posterior projections on the trigonids of the holotypes of Gobiolagus tolmachovi and G. andrewsi. Specimens found at Ulantatal resemble Ordolagus and not Gobiolagus in the above features. Nevertheless, on some specimens from Ulantatal there are various re?ntrants on P_3, apart from the main posteroexternal ones. The posterior trigonid projection on P_4 and posterointernal convex on M_2 are better developed on the Ulantatal specimens than as noted for the holotypes, these differences may be due to different developmental stages being represented by various specimens. The Ulantatal specimens are, therefore, here referred to Ordolagus teilhardi. Ordolagus teilhardi has large size and three upper molars. P~3 is fully molariform and there are bridges of enamel and dentine between the P_4-M_2 trigonids and talonids. All of these features indicate that O. teilhardi is a leporid. Specimens of Ordolagus can be distinguished from those of other leporid genera by their possession of completely molariform P~3s and greater transverse width of the upper cheek teeth. There is no evidence of a hypostria on the upper cheek teeth of Ordolagus, like Lushilagus and Shamolagus. However, Lushilagus and Shamolagus differ from Ordolagus teilhardi in their possession of several primitive features, such as smaller size, lower crowns, nonmolariform P~3, and relatively longer upper cheek teeth than seen in Ordolagus. There are no known upper cheek teeth of Gobiolagus. Li (1965, p. 27) described a broken maxilla with M~1-2 as ? Gobiolagus sp.. It is comparable to Shamolagus medius in size, possession of hypostria and greater anteroposterior width of upper cheek teeth. These features also distinguish Li's specimen from Gobiolagus. Considering the above noted similarities of lower cheek teeth between Ordolagus and Gobiolagus, it is not likely that Li's specimen belongs to either genus. Some specimens of Ordolagus teilhardi possess anteroexternal and anterointernal furrows on P_3 and other similar features of the lower cheek teeth. The common possession of these characteristics by Ordolagus sp. and Gobiolagus sp. demonstrating the close affinity of the two genera. In addition, both O. teilhardi and G. ? major the mandible is deep, trigonids possess posterior projections and M_3 is reduced in size and placed obliquely with respect to the alveolar margin. But, in general, G. ? major possesses a more primitive suite of characters than O. teilhardi, including subhypsodont, relatively longer lower cheek teeth, trigonid posterior projections less developed, M_3 with a shallow lingual groove in addition to the buccal one. It is possible that G. ? major represents an earlier branch of leporids which give rise to that of Ordolagus teilhardi. The upper cheek teeth are strongly curved in O. teilhardi due to the progressive hypsodonty in this species, as Tobien (1978, p. 171) noted. All known specimens of Ordolagus teilhardi were recovered from Middle Oligocene deposits. For that reason, the "typical" fossil leporid is considered to be of tha

本文记述了内蒙古阿左旗乌兰塔塔尔中渐新世地层中发现的兔形类材料中的一种兔科化石——德氏鄂尔多斯兔 [Ordolagus teilhardi (Burke), 1941]. 在形态上对该属种做了较多的补充和订正,并对其系统关系进行了初步探讨.

This paper attempts to make researches, within the bound of environment and investment, on exploring of the methods to plan an overall pattern of the interchange according to traffic requirement, and to discuss the problems of computer simulation and auxiliary policy-making, In this way, the classification of the interchange form is directly related to plan drawing by the medium of traffic demand, and a planning model for the interchange composition can be set up differing from the empirical ones.

本文探讨以环境和投资为约束、计算机模拟及辅助决策为手段,建立按交通需求拟定立交总图模式的规划方法。

A population of the hypotrichous ciliate Urosomoida agildermis Foissner, 1982 was found from a soil sample in Qingdao in 1986. Based on the protargol impregnation method, its morphogenesis was reinvestigated. The overall pattern of the morphogenetic events is similar to that known from most other oxytrichids. 1) It starts with a proliferation of basal bodies for the oral primordium close to the 3 posterior ventral cirri. 2) The 5 anlagen of the frontoventral cirri of the proter and the opisthe are of different...

A population of the hypotrichous ciliate Urosomoida agildermis Foissner, 1982 was found from a soil sample in Qingdao in 1986. Based on the protargol impregnation method, its morphogenesis was reinvestigated. The overall pattern of the morphogenetic events is similar to that known from most other oxytrichids. 1) It starts with a proliferation of basal bodies for the oral primordium close to the 3 posterior ventral cirri. 2) The 5 anlagen of the frontoventral cirri of the proter and the opisthe are of different origins and evolve separately. 3) In both daughter cells 5 anlagen generate 2, 2, 3 f 3-4, 3-4 frontoventral and transverse cirri. 4 ) The development of the dorsal kineties shows no special features, 3 kineties derive from 3 anlagen, the rightmost one comes from the anlage anterior to the right marginal row.A comparison with the morphogenesis of other species of the genera, e. g.Oxytricha or Steinia shows that the morphogenetic details (e. g. the site of the origin of the oral primordium, the origin of the frontoventral cirri, the mode of development of the dorsal kineties) are very similar and thus suggests a close relationship among those genera.

敏捷瘦体虫(UrosomoidaagiliformisFOISSNER,1982)为小型腹毛目纤毛虫。利用银染法对该种二分裂期间的形态发生学进行初步研究,指出该虫形态发生的主要过程为:1.伴随大核改组带的出现,口原基发生于老口围带的下方,后演化为后仔虫的口围带。在前仔虫,老口围带及口侧膜完全保留并被继承;2.体棘毛场首先出现后一组棘毛原基,后形成前棘毛场,随后各自独立演化成前后仔虫的8:3/4:2/3模式的额-腹-横棘毛;3.在背触毛中,分别于前、后仔虫的中部产生前、后3列新原基,每列原基向其两端伸展替代老背触毛列,成为前、后仔虫相应的3列新触毛;接着,在右缘棘毛原基右前端发生前、后第4列背触毛。

 
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