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61.
甘草(Glycyrrhiza uralensis)是荒漠地区具有植冠种子库的植物。成熟种子硬实率高达80%以上[1],自然条件下种子萌发率很低(约为5%-15%)[2]。本文研究了荒漠区野生甘草植冠种子库大小、种子活力、对土壤种子库的补充、种子脱落机理及植冠种子库的生态功能,指出野生甘草资源植冠种子库在甘草资源保护和恢复方面的重要作用。 相似文献
62.
微孔草的分布及植物群落特征研究 总被引:5,自引:0,他引:5
采用定量样地法,对孔微草这一特种油料植物的群落结构、群落变异以及群落特征进行了研究。结果表明,微孔草干物质生产量占总量的比率,休闲地为9.16%、撩荒地为16.90%、油草地为15.32%、燕麦地为10.66%、青稞地为5.97%;群落系数相应为87.09%、87.91%、91.82%、95.65%、93.60%;优势度相应为9.60%、13.45%、11.99%、16.61%、7.13%。经主分 相似文献
63.
植物的花序结构及其形态特征是影响种子生产性能的重要因素。对于禾本科植物而言,其花序大小、小穗数、小花数及小花的外稃、内稃和芒的性状特征直接影响种子形成和产量。本研究通过测定小黑麦品系C2、C35和黑麦品系C13、C33的花序结构特征,得到以下结果:小黑麦花序[(14.30±0.52) cm×(1.24±0.09) cm]明显大于黑麦[(13.20±0.35) cm×(0.82±0.02) cm],小黑麦花序长而粗,黑麦花序短而细;小黑麦花序的小穗数[(21.35±1.47)个]少于黑麦[(30.20±0.79)个];小黑麦每个小穗的小花数较多,为3~4朵,黑麦的小花数趋于稳定,每个小穗有2朵小花。从花序中部小穗的小花结构看,小黑麦下位护颖长[(1.27±0.11) cm]和宽[(0.26±0.03) cm]、上位护颖长[(1.30±0.09) cm]和宽[(0.23±0.04) cm]均显著大于黑麦下位护颖长[(1.04±0.05) cm]和宽[(0.08±0.01) cm]、上位护颖长[(0.94±0.10) cm]和宽[(0.06±0.01) cm];小黑麦中部小穗第1小花的外稃宽[(0.32±0.03) cm]、外稃高[(0.24±0.03) cm]和芒长[(8.35±0.51) cm]、第2小花的外稃宽[(0.35±0.04) cm]、外稃高[(0.25±0.05) cm]和芒长[(8.37±1.19) cm]极显著大于黑麦相应值[(0.26±0.01),(0.15±0.01),(5.50±0.19),(0.25±0.01),(0.17±0.01)和(5.18±0.23) cm];第1和第2小花的外稃长[(1.35±0.06),(1.37±0.06) cm]和内稃长[(0.84±0.04),(1.41±0.06) cm]均小于黑麦的外稃长[(1.49±0.05),(1.47±0.05) cm]和内稃长[(1.45±0.05),(1.47±0.04) cm]。小黑麦的穗粒数[(52.50±1.80)粒]显著低于黑麦[(58.50±2.50)粒] (P<0.05),但其穗粒重[(2.08±0.04) g]、粒重[(0.04±0.00) g]和籽粒宽[(3.04±0.32) mm]均极显著高于黑麦 (P<0.01),每个花序的籽粒不仅体积大,而且质量较重,其籽粒的生产性能高于黑麦。小黑麦籽粒呈椭圆形或长卵圆形,浅黄色,表皮皱缩,饱满度差;黑麦籽粒呈窄纺锤形,青灰色,表皮光滑,籽粒饱满。小黑麦和黑麦花序结构与籽粒性状的Pearson相关分析表明,小黑麦花序宽和花序基部小穗数与籽粒长显著正相关(P<0.05),花序长与籽粒宽极显著正相关(P<0.01),花序中部小穗的下、上位护颖宽分别与穗粒重和穗粒数极显著正相关(P<0.01);黑麦花序中部小穗第2小花的内稃长与籽粒长显著正相关(P<0.05),外稃高与穗粒数极显著负相关(P<0.01)。研究小黑麦和黑麦的花序结构和籽粒特征,对正确区分二者和了解其籽粒的生产性能具有重要意义,同时有利于小黑麦的示范推广。 相似文献
64.
燕山板栗种质资源遗传多样性的RAPD分析 总被引:4,自引:0,他引:4
为研究燕山板栗的遗传多样性,采用随机扩增多态DNA(randomamplifiedpolymorphicDNA,RAPD)技术对36份燕山板栗种质进行了分析。分析了燕山板栗的遗传丰富度,并对包括36个燕山板栗品种和8份外来板栗品种在内的44份板栗种质进行聚类分析。结果表明,RAPD能有效地区分品种间的差异,用16个随机引物经PCR扩增共得到132个片段,其中有83个多态性片段,占62.9%;不同遗传位点之间遗传多样度最大可达0.444,最小值为0.096,平均多样度为0.187;UPGMA法聚类,将44份板栗种质聚成4个大的类群,36份燕山板栗可分为3个大的类群,外来种质聚为一类。燕山板栗明显不同于外来品种。在RAPD图谱中,找到了19个品种(类型)的特异性标记和标记组合,可作为品种(类型)分子鉴别的依据。 相似文献
65.
66.
67.
甘蓝型油菜含油量的遗传研究 总被引:5,自引:0,他引:5
韩继祥 《中国油料作物学报》1990,(2)
采用7×7双列杂交设计,研究了甘蓝型油菜含油量的基因作用和其它遗传参数,以及含油量与其它农艺性状、品质性状的关系。结果表明:含油量的遗传符合加性—显性遗传模型,有关基因在亲本中呈独立分布;显性指向增效,表现超显性作用;亲本中显性基因比隐性基因多,增效基因比减效基因的频率大;控制含油量并表现显性的基因约为4组;含油量的广义和狭义遗传力分别为81.16%和30.90%。单相关和逐步回归分析一致表明,单株产量、每角粒数、主花序长度和株高对含油量有较强正向作用,但角果长度和全株总角果数的作用为负。本文还讨论了基因作用分析在探讨配合力的基因效应成分和杂种优势产生的可能原因中的意义,及其在选择中的应用。 相似文献
68.
Genetic correlations between phenotypically similar or related traits tested at young horse performance tests for Danish Warmblood (DWB) and Swedish Warmblood (SWB) horses were calculated using Multi-trait Across Country Evaluation (MACE). Data comprised stallions with an estimated breeding value (EBV) from the national genetic evaluations (NGE) based on at least 10 progeny tested in performance tests, and the ancestors of those stallions in two generations. The DWB data included 349 stallions and the SWB data 426 stallions. Of these, 28 had EBVs in both DWB and SWB. Additionally 151 pedigree animals were common between DWB and SWB. The dependent variables used were NGE results of stallions born 1980 and later, which reduced the number of common stallions with EBVs to 23. The genetic correlations were very high for jumping traits (0.99) and dressage related traits (0.89–0.97). For conformation traits correlations varied between 0.10 and 0.98. Because of the high genetic correlations and frequent use of same or closely related foreign stallions, breeders of both DWB and SWB would benefit from using the NGEs for performance traits across countries, although the genetic correlations do not consider differences in genetic merit levels between the populations. It would be feasible to perform a joint genetic evaluation using MACE, which would improve the reliability of estimated breeding values, and enable ranking of all stallions according to the national scale of each country. 相似文献
69.
Tradable biodiversity credit systems provide flexible means to resolve conflicts between development and conservation land-use
options for habitats occupied by threatened or endangered species. We describe an approach to incorporate the influence of
habitat fragmentation into the conservation value of tradable credits. Habitat fragmentation decreases gene flow, increases
rates of genetic drift and inbreeding, and increases probabilities of patch extinction. Importantly, tradable credit systems
will change the level of fragmentation over time for small and/or declining populations. We apply landscape equivalency analysis
(LEA), a generalizable, landscape-scale accounting system that assigns conservation value to habitat patches based on patch
contributions to abundance and genetic variance at landscape scales. By evaluating habitat trades using two models that vary
the relationship between dispersal behaviors and landscape patterns, we show that LEA provides a novel method for limiting
access to habitat at the landscape-scale, recognizing that the appropriate amount of migration needed to supplement patch
recruitment and to offset drift and inbreeding will vary as landscape pattern changes over time. We also found that decisions
based on probabilities of persistence alone would ignore changes in migration, genetic drift, and patch extinction that result
from habitat trades. The general principle of LEA is that habitat patches traded should make at least equivalent contributions
to rates of recruitment and migration estimated at a landscape scale. Traditional approaches for assessing the “take” and
“jeopardy” standards under the Endangered Species Act based on changes in abundance and probability of persistence may be
inadequate to prevent trades that increase fragmentation. 相似文献
70.
Andrzej Pedryc Szabolcs Ruthner Rita Hermán Boris Krska Attila Hegedűs Júlia Halász 《Scientia Horticulturae》2009
Eight polymorphic simple sequence repeat (SSR) markers located in the G1 linkage group of apricot (Prunus armeniaca L.) were previously developed and evaluated in a small set of cultivars. Those primers were used for studying variability in 77 apricot cultivars belonging to five different geographical groups, such as Chinese, Asian (Irano-Caucasian and Central Asian), North American, Mediterranean and Western European as well as Middle European cultivars. Six of the markers were polymorphic and revealed a total of 71 alleles ranging from 5 (aprigms11) to 20 (aprigms1) alleles per locus with a mean value of 11.83 alleles per locus. In conclusion, the SSR loci located in the G1 linkage group show a level of polymorphism which is similar to loci dispersed throughout the entire genome. The total number of alleles and the number of unique alleles were the highest in Chinese apricots and the lowest in Middle European cultivars. Heterozygosity also showed a decrease from Asia and China to Middle Europe. No association could have been observed between any SSR markers tested and plum pox virus (PPV) resistant phenotype of cultivars. PPV resistant cultivars did not form a separate clade on the dendrogram obtained by UPGMA cluster analysis. Middle European and Chinese cultivars formed separate clusters while other genotypes formed smaller multiple sub-groups or scattered among different clusters. Our results support previous hypotheses on the origin of PPV resistance in North American apricots. The allele data was also presented in a form that allowed the easy observation of allele frequencies in each geographical group at each locus. Using this data field, differences and similarities between cultivar groups can be easily assessed. The analysis demonstrated the links between the North American and Mediterranean apricot germplasm and confirmed that the Chinese and Eastern European cultivars are distantly related. 相似文献