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71.
3个小麦条锈菌鉴别寄主的抗性遗传分析 总被引:1,自引:1,他引:1
根据对鉴别寄主的毒性谱,选用小麦条锈病菌生理小种2E16单孢菌系为接种病菌,鉴定了小麦务锈病菌鉴别寄主Chinese166、HeinesⅦ和Vilmorin23的抗性基因构成及其遗传特征。通过对3个鉴别寄主与感病品种铭贤169杂交,分别在苗期鉴定了亲代、F1、F2、BC1及正反交后代对小种2E16的抗性反应。结果表明:供试品种Chinese166对生理小种2E16的抗性由二对显性基因,即显性基因Yr1和另一对显性基因独立或重叠控制;HeinesⅦ对生理小种2E16的抗性由一对显性基因Yr2和一对隐性基因控制;Vilmorin23对生理小种2E16的抗性则由显性基因Yr3和一对隐性基因控制。 相似文献
72.
Guillaume Garin Christian Fournier Bruno Andrieu Vianney Houlès Corinne Robert Christophe Pradal 《Annals of botany》2014,114(4):795-812
Background and Aims
Sustainable agriculture requires the identification of new, environmentally responsible strategies of crop protection. Modelling of pathosystems can allow a better understanding of the major interactions inside these dynamic systems and may lead to innovative protection strategies. In particular, functional–structural plant models (FSPMs) have been identified as a means to optimize the use of architecture-related traits. A current limitation lies in the inherent complexity of this type of modelling, and thus the purpose of this paper is to provide a framework to both extend and simplify the modelling of pathosystems using FSPMs.Methods
Different entities and interactions occurring in pathosystems were formalized in a conceptual model. A framework based on these concepts was then implemented within the open-source OpenAlea modelling platform, using the platform''s general strategy of modelling plant–environment interactions and extending it to handle plant interactions with pathogens. New developments include a generic data structure for representing lesions and dispersal units, and a series of generic protocols to communicate with objects representing the canopy and its microenvironment in the OpenAlea platform. Another development is the addition of a library of elementary models involved in pathosystem modelling. Several plant and physical models are already available in OpenAlea and can be combined in models of pathosystems using this framework approach.Key Results
Two contrasting pathosystems are implemented using the framework and illustrate its generic utility. Simulations demonstrate the framework''s ability to simulate multiscaled interactions within pathosystems, and also show that models are modular components within the framework and can be extended. This is illustrated by testing the impact of canopy architectural traits on fungal dispersal.Conclusions
This study provides a framework for modelling a large number of pathosystems using FSPMs. This structure can accommodate both previously developed models for individual aspects of pathosystems and new ones. Complex models are deconstructed into separate ‘knowledge sources’ originating from different specialist areas of expertise and these can be shared and reassembled into multidisciplinary models. The framework thus provides a beneficial tool for a potential diverse and dynamic research community. 相似文献73.
五十年代以来,小麦白秆病先后发生于我国的四川、青海和西藏的高寒地区。由于是一种摧毁性病害,很快受到有关方面的研究,测定出有效的防治措施并推广,从而限制了该病的扩展和危害。但在病原菌方面,过去国内一些研究者虽先后几经研究,不仅未能获得统一的学名且有错误的鉴定。因此,有必要再研究,以便正确地识别此菌的分类位置。作者据川、青、藏高原收集到的该菌标本及培养物切片和染色进行镜检,观察到小麦白秆病菌的产孢结构是瓶梗型的,确实应隶属于壳月孢属(Selenophoma)内,并以此菌的形态特征也不同于壳月孢属内的其它种,因而认为是一新种——小麦壳月孢(Selenophoma tritici sp.nov.),文中对新种作了形态特征的汉文和拉丁文描述和附图。此外,还阐明了现代半知菌类分类中产孢细胞的特征的重要性。模式标本存放于中国科学院微生物研究所真菌标本室(HMAS)。 相似文献
74.
75.
Marie-Louise Bouillant Jean-Louis Pittet Jacques Bernillon Jean Favre-Bonvin Noël Arpin 《Phytochemistry》1981,20(12):2705-2707
The chemical structure of the mycosporin isolated from Ascochyta pisi, Cladosporium herbarum and Septoria nodorum was established as mycosporin-2 glucoside. 相似文献
76.
Baljeet K. Gill Daryl L. Klindworth Matthew N. Rouse Jinglun Zhang Qijun Zhang Jyoti S. Sharma Chenggen Chu Yunming Long Shiaoman Chao Pablo D. Olivera Timothy L. Friesen Shaobin Zhong Yue Jin Justin D. Faris Jason D. Fiedler Elias M. Elias Shuyu Liu Xiwen Cai Steven S. Xu 《The Plant journal : for cell and molecular biology》2021,106(6):1674-1691
The resistance gene Sr13 is one of the most important genes in durum wheat for controlling stem rust caused by Puccinia graminis f. sp. tritici (Pgt). The Sr13 functional gene CNL13 has haplotypes R1, R2 and R3. The R1/R3 and R2 haplotypes were originally designated as alleles Sr13a and Sr13b, respectively. To detect additional Sr13 alleles, we developed Kompetitive allele specific PCR (KASP™) marker KASPSr13 and four semi-thermal asymmetric reverse PCR markers, rwgsnp37–rwgsnp40, based on the CNL13 sequence. These markers were shown to detect R1, R2 and R3 haplotypes in a panel of diverse tetraploid wheat accessions. We also observed the presence of Sr13 in durum line CAT-A1, although it lacked any of the known haplotypes. Sequence analysis revealed that CNL13 of CAT-A1 differed from the susceptible haplotype S1 by a single nucleotide (C2200T) in the leucine-rich repeat region and differed from the other three R haplotypes by one or two additional nucleotides, confirming that CAT-A1 carries a new (R4) haplotype. Stem rust tests on the monogenic, transgenic and mutant lines showed that R1 differed from R3 in its susceptibility to races TCMJC and THTSC, whereas R4 differed from all other haplotypes for susceptibility to TTKSK, TPPKC and TCCJC. Based on these differences, we designate the R1, R3 and R4 haplotypes as alleles Sr13a, Sr13c and Sr13d, respectively. This study indicates that Sr13d may be the primitive functional allele originating from the S1 haplotype via a point mutation, with the other three R alleles probably being derived from Sr13d through one or two additional point mutations. 相似文献
77.
DNA sequences from five nuclear loci and data from three microsatellites were collected from 360 isolates representing 14 globally distributed populations of the plant pathogenic fungus Mycosphaerella graminicola. Haplotype networks were constructed for the five sequence loci and population subdivision was assessed using Hudson's permutation test. Migration estimates were calculated using six regional populations for both the sequence and microsatellite loci. While subdivision was detected among the six regional populations, significant gene flow was indicated among some of the populations. The European and Israeli populations contributed the majority of historical immigrants to the New World. Migration estimates for microsatellite loci were used to infer more recent migration events among specific New World populations. We conclude that gene flow was an important factor in determining the demographic history of Mycosphaerella graminicola. 相似文献
78.
S. Ydergaard A. Enkegaard H. F. Brødsgaard 《Entomologia Experimentalis et Applicata》1997,85(2):177-187
Life table characteristics of Hypoaspis miles Berlese (Acarina: Hypoaspidae) fed on a mixture of Bradysia paupera Tuomikoski (Diptera: Sciaridae) and B. tritici Coquillet larvae were investigated in laboratory experiments at 4 temperatures (15, 20, 25, 30 °C) for development time, juvenile mortality, sex ratio, preoviposition period, oviposition period, postoviposition period, age-specific fecundity, and adult longevity. Juvenile development time decreased with increasing temperature from 46 days at 15 °C to 10 days at 30 °C. The lower temperature threshold was 9.9 °C and development required 205 °D. Juvenile mortality decreased from 52% at 15 °C to 3% at 25 °C and then increased to 24% at 30 °C. Preoviposition period varied with temperature from 12 days at 15 °C to 3 days at 25 °C and then increased to about 4 days at 30 °C. Oviposition period decreased with increasing temperature from 58 days at 15 °C to 25 days at 30 °C. The mean number of eggs per female per day increased from 0.4 at 15 °C to 2.3 at 25 °C and decreased to 1.3 at 30 °C. Age-specific fecundity was described by a temperature dependent model from which the maximum daily fecundity rate could be estimated to be attained at 25.6 °C. Female longevity was significantly shorter than for males, and decreased from 90 days at 15 °C to 34 days at 30 °C. Sex ratio was female-biased at all 4 temperatures and increased with temperature up to 25 °C, decreasing at 30 °C. Estimates of net reproductive rate, intrinsic rate of increase, finite rate of increase, mean generation time and doubling time were obtained. The r
m
-value increased with temperature from 0.031 day-1 at 15 °C to 0.133 day-1 at 25 °C, after which it decreased to 0.112 day-1 at 30 °C. The study showed that H. miles can develop and reproduce at temperatures between 15 and 30 °C. H. miles and sciarids have approximately the same optimum temperature and thresholds for development and reproduction and H. miles can be used for biological control of sciarids within the temperature range where the pest occurs. 相似文献
79.
Genetic Analysis and Molecular Mapping of a Stripe Rust Resistance Gene in Chinese Wheat Differential Guinong 22 下载免费PDF全文
Qian Li Yu Fan Xuexue Shen Jinxue Jing Baotong Wang Zhensheng Kang 《Journal of Phytopathology》2016,164(7-8):476-484
Stripe rust, caused by Puccinia striiformis f.sp. tritici (Pst), is one of the most damaging diseases of wheat worldwide, especially in China. Growing resistant cultivars is the most effective approach to control the disease, but few effective resistance genes are available. Guinong 22, one of the wheat cultivars used for differentiated Chinese race of the pathogen, has unknown resistance gene(s) to stripe rust. Genetic analysis, molecular mapping and allelic analysis were used in this study to determine the inheritance and chromosomal location of the gene(s) in Guinong 22 with the most prevalent Pst race CYR33. Genetic analysis indicated that a single recessive gene yrGn22 confers the resistance to CYR33. A total of 450 simple sequence repeat (SSR) primer pairs and 31 pairs of sequence‐tagged site (STS) or conserved primers were selected to screen the resistant bulk and susceptible bulk as well as the parents. Seven polymorphic SSR markers and two STS markers were then used to genotype 113 F2 individual plants. Linkage analysis indicated that all nine markers were linked to yrGn22, with genetic distances ranging from 2.2 to 11.1 cM. Based on the chromosomal locations of the linked markers, yrGn22 was located on wheat chromosome 1B near the centromere. The pedigree, common markers, chromosome location, resistance and allelism tests indicated that yrGn22 is either linked to Yr26 or possibly the same gene. 相似文献
80.
C. M. Bender Z. A. Pretorius F. J. Kloppers J. J. Spies 《Journal of Phytopathology》2000,148(2):65-76
Evidence exists that certain genes for resistance to leaf rust in wheat, e.g. Lr13 and Lr34 , may interact with other genes to condition higher levels of resistance than that conferred by each gene individually. In this study, the hypothesis that Lr12 and Lr13 , both genes for adult plant resistance to Puccinia recondita Roberge ex. Desmaz f. sp. tritici Eriks. and Henn., interact to confer an improved level of resistance, was investigated using fluorescence and phase-contrast microscopy. Flag leaf segments of monogenic and digenic Thatcher lines, sampled 64 and 240 h post-inoculation, were stained with Uvitex 2B and screened, using fluorescence microscopy, for development of infection structures or host response. To study cell wall appositions, specimens were stained with trypan blue and a solution of picric acid in methyl salicylate. Aborted penetration, consisting of nonpenetrating appressoria and aborted substomatal vesicles, showed that inhibition of fungal growth in wheat lines containing Lr12 and/or Lr13 was activated, to a certain degree, before haustoria were formed. At 240 h after inoculation colony size indicated that fungal colonies in the Lr gene combination lines were generally smaller than in the parents, but not necessarily smaller than those in a line with Lr13 only. Host cell necrosis was more frequently associated with infection sites, specifically of pathotype UVPrt2, in the combination lines than in the parents. The morphology of cell wall appositions varied considerably from a narrow, luminous zone slightly wider in the centre, to a thick central part opposite the haustorium mother cell, sharply decreasing towards both ends. Histological assessments could, however, not conclusively prove pronounced resistance enhancement or unconventional resistance mechanisms due to combining the genes Lr12 and Lr13 . 相似文献