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1.
Wheat grain yield consists of three components: spikes per plant, grains per spike (i.e. head or ear), and grain weight; and the grains per spike can be dissected into two subcomponents: spikelets per spike and grains per spikelet. An increase in any of these components will directly contribute to grain yield. Wheat morphology biology tells that a wheat plant has no lateral meristem that forms any branching shoot or spike. In this study, we report two novel shoot and spike traits that were produced from lateral meristems in bread wheat. One is supernumerary shoot that was developed from an axillary bud at the axil of leaves on the elongated internodes of the main stem. The other is supernumerary spike that was generated from a spikelet meristem on a spike. In addition, supernumerary spikelets were generated on the same rachis node of the spike in the plant that had supernumerary shoot and spikes. All of these supernumerary shoots/spikes/spikelets found in the super wheat plants produced normal fertility and seeds, displaying huge yield potential in bread wheat.  相似文献   

2.
Yield studies show that increases in grain yield are always accompanied by an increase in grain number and, hence, further increases in yield potential may require additional improvements in grain number. The improvement of modern durum wheat was mainly based on the introduction of semidwarf genes. A 2‐year field drought stress experiment, concerning two different genotype groups (landraces vs modern cultivars), was carried out under a rainout shelter in order (a) to assess the effect of water deficit on floret dynamics and grain number determination, (b) to explore the relationship between plant water status with grain number per spike and its components (i.e., spikelets per spike, fertile florets per spikelet and grain set) and (c) to quantify the importance of several plant traits in determining the final number of grains per spike and fertile florets per spike when the main source of variation is water availability. Compared to control (well irrigated), grain number per spike was reduced, depending on year, genotype and water availability level, by 12.4–58.7% and this reduction was evident almost in all spikelet positions along the spike. Although there were some doubts in the past about the increased sensitivity of semidwarf cultivars to drought stress, they were not confirmed from our results. In most of the cases, the variation in plant water status (by means of water potential index [WPI]) during floret primordia phase (FPP) explained most of the variance in grain number per spike, fertile florets per spikelet, grain set and fertile spikelets per spike. In general, increasing water stress intensity decreased grain number per spike by an average rate of 13.5 and 9.4 grains per 0.2 MPa decrease in WPI, in modern cultivars and landraces, respectively. However, seasonal and genotypic effects were evident by modifying the slopes of the linear regressions between WPI and the studied plant traits. Commonality analysis revealed that the number of fertile florets per spikelet was the best predictor of grain number per spike, indicating that there is still much space for further improvement for this trait in landraces. However, this trait has been clearly improved in modern cultivars, especially at the basal and central spikelets. Although the number of spikelets per spike was the best unique predictor of the number of grains per spike in modern cultivars, grain set presented the highest total effect.  相似文献   

3.
Summary Heritability estimates of five characters of the wheat plant were studied in five crosses involving six cultivars of bread wheat. Parents, F1, F2 and backcrosses to both parents were used in the estimation of the genetic parameters.Heritability was low for number of fertile spikes/plant, moderate for number of spikelets/spike, number of kernels/spike, 1000-kernel weight and moderately high for number of kernels/spike. Evidence for mainly nonadditive gene effects were observed in the expression of number of fertile spikes and 1000-kernel weight. Although nonadditives contributed to a lesser degree to the gene action, additives seemed to be the most important genetic expression regulating number of spikelets/spike, number of kernels/spike, and number of kernels/spikelet. Except for number of fertile spikes/plant, selection in F2-populations seems to be promising.  相似文献   

4.
疏剪不同穗位小穗对小麦籽粒结实和粒重的影响   总被引:1,自引:0,他引:1  
1997~1998年在河南省农作物品种展览中心以中大穗小麦品种温麦6号为材料,设计了去除不同穗位小穗的试验。结果表明,去除不同位小穗对结实粒数和粒重的影响不同, 除顶端小穗的粒数下降较多,穗粒重最低,却除基部小重申对结实粒数和粒重的影响较小,穗粒数和粒重下降较少;却除中部小穗对结实粒数影响较大,穗粒数量小,其穗粒重因剩余籽粒单粒重增加而得以一定程度补偿。  相似文献   

5.
The realization of grain yield in wheat is decided by source-sink balance under prevailing environmental conditions. Management conditions like changing the sowing time influence the source-sink capacity through modification in agronomic traits. Therefore, this experiment was conducted to decipher the influence of spike architectural traits (SATs) on grain yield and to open avenues for further grain yield enhancement. Comparatively early sowing over timely sowing gives the advantage of realizing higher grain yield with a positive relationship with SATs namely spike length, spikelets per spike, individual spike weight, individual grain weight, number of grains per spikelet, grain length, and grain width of upper and lower spike portion. Confirmatory factorial analysis revealed that spike length, spikelets per spike, individual spike weight, grains per spikelet were having a significant effect in deciding grain yield in early sown. The presence of a significant effect of genotype by environment interaction over grain yield and SATs allows the exploitation of available genotypic and environmental variability for further yield enhancement. GGE analysis on transformed and standardized grain yield-trait (GY-trait) combinations was used in the selection of genotypes having high GY-trait combinations for both sowing times. In early sowing, WG 11 was the best for high GY with high individual spike weight; grain length and grain width at lower and upper parts of the spike; and shorter days to 50% flowering. Genotypes exclusively having the high GY-trait combination along with low values of remaining GY-trait combinations were also selected with genotype focused GGE approach.  相似文献   

6.
在大田栽培条件下,研究开放式空气CO2浓度增加(FACE)200μmol·mol-1的处理对水稻产量及产量构成因素的影响.结果表明,FACE处理对水稻株高和主茎叶片数没有明显影响,但使水稻生育进程加快,全生育期显著缩短,增加施N量可减缓FACE处理对水稻全生育期缩短的程度;FACE处理能显著增加分蘖数,极显著增加穗数,提高结实率,但使每穗颖花数显著减少;FACE处理能显著提高水稻产量,在高N条件下增产幅度更大;提高FACE处理的每穗颖花数和单位面积颖花数能极显著提高水稻产量,增加施N量是提高FACE处理每穗颖花数和单位面积颖花数的重要措施.  相似文献   

7.
Decapitation induced an additional formation of secondary shoots and anomalous spikes in all the species. The moan numbers of nodes, spikelets per spike, seeds per spikelet and spike, and the mean length of the stem and spike were reduced on secondary shoots of decapitated plants, while the mean and peak numbers of flowers per spikelet and the peak number of seeds per spikelet increased. The increase in the number of flowers per spikelet was the most striking on spike base; the seeds regularly occurred even in spikelets with an expressively increased number of flowers. The post-decapitation changes of the spike could be well expressed quantitatively according to the increased mean number of the flowers per one seed. Morphological ohanges in anomalous spikes of all the wheat species resemble phylogenetic reversions described in literature. Moreover, the peak numbers of flowers and seeds per spikelet were recorded in 52 varieties belonging to 21 wheat species. As compared with the decapitation trial, the greatest variability and the greatest differences between the speoies were also reoorded in the tetraploid group, and the smallest variability and differences between the species in the diploid group. We suppose that the striking morphological differences in post-decapitation spikes take place because the apical dominance was interrupted before differentiation of the recent form had been controlled in meristems on the decapitated stem base. Ancestral forms were morphologically realized with the help of an assimilating part of the decapitated stem.  相似文献   

8.
Increasingly, wheat (Triticum aestivumL.) is being grown intropical environments, but there is inadequate information aboutthe physiological processes limiting yield. In this investigation,the source:sink ratio was manipulated to examine the performanceof source-sink interactions after anthesis and the factor(s)limiting grain filling in tropical conditions. Plants of threewheat cultivars, Cuba C-204, Candeias and IAC-60, were artificiallymodified to give different source:sink ratios. The treatmentswere: I, Control; II, all spikelets on one side of the spikeremoved; III, all spikelets removed except the four centralspikelets of the spike; and IV, flag leaf blade removed. Thedistribution of dry matter between kernels and stem internodeswas analysed at harvest in all three cultivars. Partitioningof14C-photoassimilates was measured on three occasions afteranthesis in the cultivar Cuba C-204. Modifications of source:sinkratio led to different patterns of allocation of dry matterbetween cultivars and sowing dates. The reduction in sink sizein treatment II produced no significant change in the mass pergrain in the January sowing, but this was enhanced in two cultivarsin the November sowing. In treatment III, both mass per grainand translocation of14C-photoassimilates declined, apparentlydue to feedback inhibition of photosynthesis. The participationof stem reserves in grain filling and the existence of genotypicdifferences in response to availability of photoassimilateswere corroborated. The pattern of partitioning of dry matterobserved in plants in this investigation suggests a source limitation,particularly during the November sowing. This pattern differedmarkedly from that in other studies, most of which have beenmade in temperate areas.Copyright 1999 Annals of Botany Company Photoassimilates, sink, source, partitioning, grain filling, wheat.  相似文献   

9.
Kernel number per spike (KNPS) is one of the key factors affecting wheat yield, which can be significantly reduced by lower fertility or sterility of the apical and basal spikelets. In this study, the spikelet number per spike (SNPS), thousand kernel weight (TKW), KNPS, total grain numbers of the top three apical spikelets (GNAS), and total grain numbers of the bottom three basal spikelets (GNBS) of 212 wheat lines were recorded from five different environmental conditions. These 212 accessions were genotyped using the 9K iSelect SNP Beadchip. A total of 3269 SNP markers were used for genome-wide association analysis (GWAS). One hundred twelve significant marker-trait associations (MTAs) were identified. Twenty-two MTAs were identified in at least two environments and two of them showed association with two or more grain setting properties. Different loci showed an additive effect with both GNAS and GNBS being much higher in the lines with more favorite alleles. Two SNP loci, wsnp_Ex_c31799_40545376 and wsnp_BF293620A_Ta_2_3, showed the largest effects on increasing KNPS through improved fertility of apical and basal spikelets, respectively. These MTAs have the potential to be used in future marker-assisted selection.  相似文献   

10.
Wu X  Chang X  Jing R 《PloS one》2012,7(2):e31249

Background

Grain yield is a key economic driver of successful wheat production. Due to its complex nature, little is known regarding its genetic control. The goal of this study was to identify important quantitative trait loci (QTL) directly and indirectly affecting grain yield using doubled haploid lines derived from a cross between Hanxuan 10 and Lumai 14.

Methodology/Principal Findings

Ten yield-associated traits, including yield per plant (YP), number of spikes per plant (NSP), number of grains per spike (NGS), one-thousand grain weight (TGW), total number of spikelets per spike (TNSS), number of sterile spikelets per spike (NSSS), proportion of fertile spikelets per spike (PFSS), spike length (SL), density of spikelets per spike (DSS) and plant height (PH), were assessed across 14 (for YP) to 23 (for TGW) year × location × water regime environments in China. Then, the genetic effects were partitioned into additive main effects (a), epistatic main effects (aa) and their environment interaction effects (ae and aae) by using composite interval mapping in a mixed linear model.

Conclusions/Significance

Twelve (YP) to 33 (PH) QTLs were identified on all 21 chromosomes except 6D. QTLs were more frequently observed on chromosomes 1B, 2B, 2D, 5A and 6B, and were concentrated in a few regions on individual chromosomes, exemplified by three striking yield-related QTL clusters on chromosomes 2B, 1B and 4B that explained the correlations between YP and other traits. The additive main-effect QTLs contributed more phenotypic variation than the epistasis and environmental interaction. Consistent with agronomic analyses, a group of progeny derived by selecting TGW and NGS, with higher grain yield, had an increased frequency of QTL for high YP, NGS, TGW, TNSS, PFSS, SL, PH and fewer NSSS, when compared to low yielding progeny. This indicated that it is feasible by marker-assisted selection to facilitate wheat production.  相似文献   

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