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late maturing cultivar
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  “late maturing cultivar”译为未确定词的双语例句
     In this experiment, three cultivars, early maturing cultivar NEA303, medium maturingcultivar Xishu 1 and late maturing cultivar jinshu 7, were used as plant materials. L_(12)(4×3 ̄3)orthogonal experimental design was adopted and indoor and outdoor experimentswere carried out, rcspcctively. The days for potato tuber to sprout were decreased with ineease in tcmpcrature.
     本试验以早熟品种东农303、中熟品种系薯1号和晚熟品种晋薯7号为试验材料,采用L12(4×3 ̄2)正交试验法,分室内和室外两组同时进行试验,结果表明,出芽天数随着温度的上升而减少;
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  相似匹配句对
     There are precocity, middle, late maturing ;
     依红心柚成熟期将其分为早熟红心柚、中熟红心柚、晚熟红心柚3类;
短句来源
     A Late Maturing Longan Variety‘Songfengben’
     晚熟龙眼新品种‘松风本’
短句来源
     Never to be late
     改变恶习 永不太迟
短句来源
     It was too Late!
     太迟了!
短句来源
     The correlation coefficients were increased when the data from late-maturing cultivars were subtracted.
     三种分析结果间的相关分析表明,大多数情况下相关系数均迭极显著程度。
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  late maturing cultivar
On the other hand, the late maturing cultivar, Howaito-roppen, formed bulblets after a low temperature treatment of the proliferated shoots for 6 months followed by culture on LS medium containing 6 to 12% sucrose for two months.
      
Rhizobial inoculation increased total N and grain yield of early maturing cultivars IAC 100 and TGX 1456-2E but did not affect the late maturing cultivar TGX 1660-19F.
      
Serrana INTA is a late maturing cultivar with smooth, white-skinned, oblong tubers of excellent appearance and uniformity.
      


The mophogenesis of the flower bud of Chinese kale could be divided into six stages:(1)the non-differentiation stage,(2)the pre-differentiation stage,(8)the initial differentiation stage,(4)the sepal formationstage,(5)the carpel and stamen differentiatingand developing stage,(6)the petal formation stage.The differentiation sequence of flower partswas:sepal,carpel,stamen and finally petal.By sowing at the same time,the early-maturing cultivar was the earliest to differentiate and the differentiation...

The mophogenesis of the flower bud of Chinese kale could be divided into six stages:(1)the non-differentiation stage,(2)the pre-differentiation stage,(8)the initial differentiation stage,(4)the sepal formationstage,(5)the carpel and stamen differentiatingand developing stage,(6)the petal formation stage.The differentiation sequence of flower partswas:sepal,carpel,stamen and finally petal.By sowing at the same time,the early-maturing cultivar was the earliest to differentiate and the differentiation occurred at lower nodes,the late-maturing cultivar was the latest to differentiate and at the higher nodes and the mid-maturing cultivar in between the two.Chinese kale was sown at different times from July to December in Guangzhou.The result indicated that flower bud differentiation of those sown in September and October was the earliest,those sown in July and August the next,and those sown in November and December the latest,and with the sowing time being delayed,the number of extended leaves decreased,and the differentiatire nodes became lower.Vernalizationtests with treatment at 3±1℃and 8±1℃ for 7,14 and 21 days on two cultivars ofChinese kale were made.The result indicated that these treatments had no significant effect on differentiates time and differentiative node of the early-maturing cultivar.However,the different treatments in the mid-and late-maturing cultivars could make their flower bud differentiation occur earlier and the differentiate node lower by some degrees.

本文研究了芥兰(Brassica alboglabra Bailey)花芽形态发育,不同播期和春化条件对芥兰不同品种花芽分化的影响。 芥兰的花芽形态发育可分为6期:1.花芽未分化期,2.花芽将分化期,3.花芽分化始期;4.萼片分化期;5.雌雄蕊分化和形成期,6.花瓣分化发育期。花器官的分化顺序是萼片、雌雄蕊、然后是花瓣。 早、中、迟熟品种同时播种表明,早芥兰的花芽分化期最早,分化叶位最低,迟芥兰的花芽分化期最迟,分化叶位最高,中芥兰则介于两者之间。 芥兰(中迟芥兰品种)在广州7~12月分期播种,以9~10月播种的花芽分化期最早,7~8月播种的较迟,11~12月播种的最迟。随着播种期的延迟,花芽分化时的展叶数逐渐减少,分化叶位逐渐降低。 3±1℃和8±1℃春化处理7、14和21天,对早芥兰的花芽分化期和分化叶位没有明显影响,中迟芥兰则不同程度地提早花芽分化和降低分化叶位。

Foliar spray of GA8 ( l00mg/ 1 ) on a Japanese persimmon'Miyaza-ki-tanenashi' ( a very late-maturing cultivar ) at the end of stage Ⅱ of fruit growth ( 19, Oct. ) inhibited the development of fruit maturation, fruit growth, coloration, sugar accumulation and the increase of endo -genous ABA content, but increased endogenous GAs like activity. On the other hand, spray of ethrel ( 25mg/l ) on another mid maturing cultivar 'Fuyu' at the begining of stage Ⅲ(1, Oct. ) hastened fruit...

Foliar spray of GA8 ( l00mg/ 1 ) on a Japanese persimmon'Miyaza-ki-tanenashi' ( a very late-maturing cultivar ) at the end of stage Ⅱ of fruit growth ( 19, Oct. ) inhibited the development of fruit maturation, fruit growth, coloration, sugar accumulation and the increase of endo -genous ABA content, but increased endogenous GAs like activity. On the other hand, spray of ethrel ( 25mg/l ) on another mid maturing cultivar 'Fuyu' at the begining of stage Ⅲ(1, Oct. ) hastened fruit maturation and the decline of endogenous GAs like activity, but promoted fruit eo-loration, softening, sugar accumulation and increased the contents of reducing sugars and endogenous ABA. The relationship between the plant growth regulators and fruit maturation was discussed in detail.

选用柿极晚熟品种宫崎无核,于果实发育第二期末(10月19日),叶面喷施100ppm的GA_3明显地抑制了果实的肥大生长、着色、糖的积累及果肉软化。对果实内源GAs活性和ABA含量进行分析的结果表明,叶面喷施GA_3使内源GAs活性大大提高,同时使ABA的增加受到抑制。与GA_3处理相反,果实发育第三期(10月1日),对中熟品种富有进行25ppm乙烯利的叶面喷施处理,明显地促进了果实的成熟,其作用尤以促进着色、加速果实软化最为明显。对内源GAs活性及ABA含量亦有明显影响,前者因乙烯利处理而降低,后者则因乙烯利处理而增大。

In this experiment, three cultivars, early maturing cultivar NEA303, medium maturingcultivar Xishu 1 and late maturing cultivar jinshu 7, were used as plant materials. L_(12)(4×3 ̄3)orthogonal experimental design was adopted and indoor and outdoor experimentswere carried out, rcspcctively. The days for potato tuber to sprout were decreased with ineease in tcmpcrature. The sprout number on large tubers was significant higher than that onsmall and mcdium tubcrs. The sprout number on tubers was decreased with...

In this experiment, three cultivars, early maturing cultivar NEA303, medium maturingcultivar Xishu 1 and late maturing cultivar jinshu 7, were used as plant materials. L_(12)(4×3 ̄3)orthogonal experimental design was adopted and indoor and outdoor experimentswere carried out, rcspcctively. The days for potato tuber to sprout were decreased with ineease in tcmpcrature. The sprout number on large tubers was significant higher than that onsmall and mcdium tubcrs. The sprout number on tubers was decreased with increase in timesof taking out sprouts. The sprout number of cv. Xishu 1 was significant higher than cv. Jinshu7 but the diffcrence bctween cvs. Xishu 1 and NEA303 was not significant. The progeny tuberyield was innuenced by cultivar and mother tuber size. The yield derived from sprouts takenat different times shown no difference but the yield from mother tuber was significant higherthan that derived from sprouts. This experiment indicated that the virus-free potatoes couldbe multiplied rapidly by taking sprouts out up to thrce timcs for transplanting and thendirectly sowing mothcr tubers.

本试验以早熟品种东农303、中熟品种系薯1号和晚熟品种晋薯7号为试验材料,采用L12(4×3 ̄2)正交试验法,分室内和室外两组同时进行试验,结果表明,出芽天数随着温度的上升而减少;大薯块出芽数极显著高于中小薯块;出芽数则随着掰芽次数的增加而减少;系薯1号的出芽数明显高于晋薯7号,与东农303差异不显著.产量结果表明,主因素为品种;其次为薯块大小;掰芽次数间差异不显著;母薯则极显著高于掰芽次数.综合结果分析,脱毒马铃薯掰芽扩繁是一项节省种薯,提高繁殖系数的有效措施;以选择适宜当地种植的高产高效和大薯块掰芽为好;三次掰芽扩繁移栽和母薯直播是可行的马铃薯扩繁技术措施.

 
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