对小麦顶生小穗的初步研究

1.顶生小穗的护颖具有特殊的形态,第二护颖常为小花外稃状,腋内有时还保留着雌雄蕊或内稃残余。说明其不稳定和可变的本质。2.顶生小穗具特殊的坐落位置,其小穗轴与主穗轴一致。顶生小穗原始体发生在穗生长锥顶端,其下无苞原始体,长成后也无小穗领。其护颖和小花外稃与侧生小穗下的小穗领呈严格连续互生状态。说明其一次轴的渊源。3.顶生小穗护颖腋内可长出小穗,小花也可代之以小穗,护颖和小花外稃有时以苞片的形式保留于新侧生小穗外侧。新顶生小穗的护颖来自小花外稃。说明顶生小穗护颖腋内的退化花芽、外稃腋内的小花与侧生小穗都是花序一次轴上的二次轴分枝。4.顶生小穗产生小穗的变异严格按自下而上的顺序进行,与原侧生小穗有严格的连续性。5.事实证明,顶生小穗是一次轴花序,它属于穗状花序顶端的可变部分。     

小麦的穗领在系统演化和个体发育中形成过程的初步探讨

小麦的穗领有三种类型:领腹完全敞开的U形穗领、领腹完全闭合的O形穗领和领腹呈V型交叉的V形穗领。穗领是系统演化中顶生叶叶鞘减化后的遗迹,也是个体发育中穗轴基部第一侧生小穗下苞叶原始体的痕迹。在一定条件下,从穗领可以长出叶鞘和叶片,穗轴基部节间可以变为茎节间,穗领腋内的小穗可以变为腋芽、带柄分枝穗或分枝花序。其余侧生小穗下都有一个领腹完全敞开的U形小穗领,其形态与U形穗领相似。它们是系统演化中二次轴分枝花序的苞叶叶鞘减化后的遗迹,也是个体发育中苞原始体的痕迹。一定条件下,从小穗领也可以长出叶鞘和叶片。穗轴基部节间变茎的同时,基部几个小穗若发生向圆锥花序的部分返祖变异,随着变异程度加深,从穗领和小穗领逐渐形成叶鞘和叶片。说明在系统演化中。顶生叶和苞叶先减化叶片,后减化叶鞘,最后形成穗领和小穗领。小麦祖先的花序与茎叶之间没有明显的界限。     

Effects of exogenous hormones on floret development and grain setin wheat

At specific stages during floret development, solutions of IAA,GA₃, zeatin and ABA were injected into the leaf sheath around theyoung spike of wheat (Triticum aestivum L.) to study theregulating effects of exogenous hormones on floret development. Zeatin promotedfloret development and significantly increased the number of fertile florets aswell as grain set, especially at the stage of anther-lobe formation. Zeatinalsoincreased the sugar concentrations in spikes at anthesis. In contrast, IAA,GA₃ and ABA inhibited floret development, with different patternsforeach of the hormones. IAA inhibited the development of the whole spike and allflorets in the spikelets such that grain loss occurred in all positions in thespikelets. GA₃ increased the number of fertile florets per spike,butdecreased grain set of the third floret in each spikelet, especially whenapplied at terminal spikelet formation. ABA inhibited floret development, anddecreased the number of fertile florets and grain set at almost all developmentstages, except at anther-lobe formation. The inhibitory effect of ABA wasmainlyon the first and third florets in each spikelet.     

Floret Initiation and Development in Spring Wheat (Triticum aestivum L.)

The number and developmental stages of florets were determinedin each spikelet of the spike in the main shoots of spring wheat.Samples were taken frequently from plants grown in a phytotronand in a nitrogen application field-test. Ten stages of development,from floret initiation until anthesis, were recognized and described. Inter-spikelet variation in the total number of initiated floretswas rather small. However, the number of florets at advancedstages of development, as well as the number of grains, washighest in the central spikelets in which florets initiatedfirst. Floret initiation did not proceed beyond spike emergence,whereafter the distal florets and the spikelet apex degenerated.Grain-set was restricted to florets which had developed at leastto the stage of visible anther lobes at spike emergence. Thenumber of these florets was increased significantly by nitrogenapplication. Wheat, Triticum aestivum L., spikelet, floret, grain set, nitrogen     

Effect of photoperiod on development and number of spikelets of a temperate and some low-latitude wheats

Four low-latitude cultivars (two Mexican and two Rhodesian) and a Canadian cultivar were grown in controlled environments in four photo-periods, 16, 13, 10 and 7 h, respectively. Plants of two of the low-latitude cultivars were also transferred between long and short photoperiods during ear differentiation. The intervals from sowing to successive stages of ear development up to the formation of the terminal spikelet, and to ear emergence, and the number of leaves, all increased as photoperiod decreased. The Canadian cultivar responded most and one of the Rhodesian cultivars least to changes of photoperiod in these respects. However, with all the low-latitude cultivars, the interval between formation of the terminal spikelet and emergence of the ear responded similarly and relatively little to decreasing photoperiod except when photoperiod was reduced from 10 to 7 h. The mean rate of spikelet production decreased as the duration of the period of spikelet production (DSP) increased, i.e. as ear development slowed down with decrease in photoperiod. Accordingly number of spikelets per ear increased curvilinearly as DSP increased, suggesting a maximal number of spikelets of about thirty. Rate of spikelet production apparently differed between cultivars. Development of the ear slowed down when plants were moved to a shorter photoperiod and accelerated when they were moved to a longer photoperiod, both at the time at which the shoot apex began to elongate and at the double ridge stage. Final number of spikelets per ear increased when ear development was slowed down and decreased when it was accelerated.     

Effect of Photoperiod and Chlormequat on Apical Development and Growth in a Spring Wheat (Triticum aestivum) Cultivar

Spring wheat, cv. Timmo, was grown under three photoperiod regimes(16, 13 and 11 h) with and without treatment with the plantgrowth regulator chlormequat (applied at the glume primordiumstage of apical development) and the relationships between apicaldevelopment, primordium initiation and growth stage examined The effects of photoperiod were generally similar to those reportedfrom other studies; shorter photoperiod slowed the rate of apicaldevelopment, increased the duration of the primordium initiationphases and reduced the rate of primordium initiation. The finalnumber of spikelets was increased, but there was no effect onnumber of floret primordia per spikelet The number of tillersproduced was also higher in the shorter photoperiods. Chlormequattreatment had a similar effect to imposing short-days: floweringwas delayed and tiller production increased There were strong correlations between certain development eventsand the phasing of primordium initiation and growth stages andthese were not affected by photoperiod or chlormequat treatments.For example, the end of spikelet primordium initiation, i.e.terminal spikelet (TS) formation, coincided with the floret-stamenprimordium stage (of the most advanced spikelet) and the endof floret primordium initiation with the stigma tic branchesand hairs on ovary wall elongating stage. Similarly, rapid stemextension growth always started at TS formation while spikeextension and spike growth commenced at TS formation and thestigmatic branches stage, respectively. Tiller production alsoceased at TS formation, when rapid stem growth started Although the timing of the phases of primordium initiation andcertain growth events were linked to apical development, therate of apical development did not determine either the rateof spikelet primordium initiation or the rates of stem and eargrowth. However, there was a strong relationship between rateof development and rate of floret primordium initiation. Therewas also a strong relationship between spike length and apicaldevelopment stage Triticum aestivum, spring wheat, photoperiod, chlormequat, apical development, primordium initiation, stem and spike growth     

Effect of decapitation on morphogenesis of stem and spike in various wheat species

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.     

Studies on the relationship between air temperature and the differentiation of young spikes of winter wheat in Beijing district

In these studies the optimum temperature indices for spikelet differentiation were found. The critical period determining the number of spikelets on a spike lies between the single ridge stage and the stage of glume differentiation. During this period a daily temperature below 7.5°C is favourable for differentiation of further spikelets. The processes of differentiation of wheat spikes need certain accumulated temperatures for a mean daily temperature above 0°C. The relationship between the rate of spikelet differentiation and temperature during the differentiation period, and the of these periods are discussed. According to the effect of climate in early spring on the number of differentiated spikelets of winter wheat, three climatic types in early spring are suggested.     

Reproductive Development in Lolium temulentum L.: Spike Morphogenesis and Grain Set Limitations

Reproductive development in cereals is not easy to investigatebecause their quantitative response to environmental factorsmakes it difficult to synchronize the plants. In this paper,one of our aims was to assess whether Lolium temulentum strainCeres, a qualitative long-day grass, could serve as a modelof reproductive development for cereals. The morphological patternsfrom floral transition to seed set were studied. A flowering scale was established to evaluate developmentalrate during spike morphogenesis. Apex growth was found to increaseaccording to biphasic kinetics; double ridge appearance markedthe beginning of an exponential phase. Developmental progression and apical growth rate were both increasedby giving repeated long days. In contrast, the final numberof lateral spikelets (20–25) could not be manipulatedafter the beginning of long-day treatment. When plants were kept in continuous light from the beginningof induction, double ridges appeared on the fifth 24 h cycle.Spikelet initiation began in the upper mid-part of the spike,and then extended acro- and basipetally. The phase of spikeletinitiation lasted 6 d, with l?5 to 1?9 spikelets being produceddaily. Within each spikelet, florets were initiated at an averagerate of l?3 primordia per day and developed acropetally. Thefirst signs of apical site degeneration were observed in themost developed upper spikelets just before heading. Ear emergenceoccurred between the 20th and 25th cycles of continuous light;anthesis was observed 6 or 7 d later. The proportion of floretssetting grain averaged about 40%. Grains were produced mainlyin the lower spikelets while the upper mid-part of the inflorescenceshowed a much lower fertility rate. Complex developmental gradients described in this paper suggestthat L. temulentum could serve as a model of reproductive developmentin cereals, with the added advantage of flowering in responseto a single long-day. Key words: Lolium temulentum L., spike morphogenesis, spikelet number, floret number, grain set     

Analysis of the spaceflight effects on growth and development of Super Dwarf wheat grown on the Space Station Mir.

The hypothesis being tested is that Super Dwarf wheat, Triticum aestivum L., plants in the Svet Greenhouse onboard the Russian Space Station Mir will complete a life cycle in spaceflight, providing that the environmental conditions necessary for adequate growth on Earth are supplied. Twenty six seeds of wheat were planted in each of 2 rows of 2 root compartments for a total of 104 seeds in Svet. Germination rate at 7 d was 56 and 73% on Mir and 75 and 90% in ground-based controls. Plants were grown throughout the whole cycle of ontogenesis (123 d) with samples gathered at different times to validate the morphological and reproductive stages of the plants. Young plants showed vigorous early seedling growth, with large biomass production, including the formation of 280 floral spikes. Upon return to Earth, comparative analyses showed that the number of tillers and flowers per spikelet were 63.2% and 40% greater, respectively, in Mir-grown plants than in the controls. By contrast, the stem length (52.4%), spike mass (49.2%) and length (23.1%), awn length (75.7%), number of spikelets per spike (42.8%) and number of seeds per spike (100% sterile) from Mir-grown plants were substantially less than the controls. Distribution of moisture and roots throughout the substrate was very good. All florets on Mir-grown spikes ceased development at the same stage of ontogeny. Lack of caryopses formation was attributed to male sterility occurring at different stages of staminal development. Anthers failed to dehisce and pollen grains were smaller and shriveled compared to the controls, suggesting a chronic stress had occurred in the Svet growth chamber. Recent ground-based studies indicated that ethylene, which was measured at 0.3 to 1.8 mg kg-1 in the Mir, almost certainly could have induced male sterility in the wheat plants grown on the Mir.     

The effect of growth retardant application on floret site utilisation and assimilate distribution in ears of perennial ryegrass cv. S.24

Application of the growth retardant paclobutrazol (PP333), at 2 kg a.i. ha^-1 at spikelet initiation to plots of perennial ryegrass cv. S.24 in 1981 and 1982 significantly increased the number of seeds per spikelet present at final harvest by reducing the number of seeds aborted during seed development. Distribution of florets and seeds per spikelet was altered by PP333, as both basal and penultimate spikelets contained more florets and seeds than did those of untreated plants. Seed weight and germination were increased in florets of penultimate spikelets, although PP333 application delayed maturity by 3–5 days. In untreated plants, assimilate recovery was significantly lower from the terminal section of the ear, whereas in PP333 treated plants, no differences were found between basal, intermediate or terminal sections of the ear. PP333 increased assimilate demand at all sections of the ear when the ear and leaves were fed. The implications of this are discussed.     

Deciphering the environmental impact on spike architectural traits for grain yield consolidation in bread wheat (T. aestivum L.)

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.     

Interactions between SQUAMOSA and SHORT VEGETATIVE PHASE MADS-box proteins regulate meristem transitions during wheat spike development

Inflorescence architecture is an important determinant of crop productivity. The number of spikelets produced by the wheat inflorescence meristem (IM) before its transition to a terminal spikelet (TS) influences the maximum number of grains per spike. Wheat MADS-box genes VERNALIZATION 1 (VRN1) and FRUITFULL 2 (FUL2) (in the SQUAMOSA-clade) are essential to promote the transition from IM to TS and for spikelet development. Here we show that SQUAMOSA genes contribute to spikelet identity by repressing MADS-box genes VEGETATIVE TO REPRODUCTIVE TRANSITION 2 (VRT2), SHORT VEGETATIVE PHASE 1 (SVP1), and SVP3 in the SVP clade. Constitutive expression of VRT2 resulted in leafy glumes and lemmas, reversion of spikelets to spikes, and downregulation of MADS-box genes involved in floret development, whereas the vrt2 mutant reduced vegetative characteristics in spikelets of squamosa mutants. Interestingly, the vrt2 svp1 mutant showed similar phenotypes to squamosa mutants regarding heading time, plant height, and spikelets per spike, but it exhibited unusual axillary inflorescences in the elongating stem. We propose that SQUAMOSA–SVP interactions are important to promote heading, formation of the TS, and stem elongation during the early reproductive phase, and that downregulation of SVP genes is then necessary for normal spikelet and floral development. Manipulating SVP and SQUAMOSA genes can contribute to engineering spike architectures with improved productivity.

Functional characterization of developmental genes reveals ways to modify the wheat spike architecture to increase the number of grains and improve productivity.     

小麦不同种植密度粒重分布特性的研究

对３种种植密度条件下小麦粒重分布特性的研究结果表明：小穗粒重、小穗结实粒数、各粒位粒重和结实数均以中下部小穗为最大,随植株密度的增大,穗粒重和穗粒数呈逐渐减小的趋势,小穗粒重、小穗结实粒数、各粒位的粒重和结实数也呈下降的趋势;不同粒位间的粒重,在结实数大于０．９５的情况下,表现为第２＞１＞３＞４粒位,在其它情况下则表现为第１＞２＞３＞４粒位     

Soluble Carbohydrates and Floret Fertility in Wheat in Relation to Population Density Stress

Wheat, variety Sonalika, was grown at different densities inboth field and pots during the winter seasons 1983–84and 1984–85. Grain yield pattern of the spikelets of themain shoot inflorescence was similar in both the field and pots,the spikelets in the middle part of the ear contributed mostand yield per spikelet decreased progressively towards the apexand the base. Increased population density decreased yield ofgrain, primarily by decreasing spikelet number and the fertilityof florets. High population density accelerated growth of thespike for some time during the pre-anthesis period and the solublecarbohydrate concentration was also higher under these conditions.During both anthesis and post-anthesis, the soluble carbohydrateconcentration and the growth of the spike declined much fasterin the high-density population. High density also decreasedthe floret fertility and growth in dry weight in all the spikelets,but it was more severe on the basal spikelets, resulting incomplete sterility of the florets at these nodes. The solublecarbohydrate concentration of these slow-growing, sterile, basalspikelets was found to be higher in comparison to that of fertilespikelets in the middle and top positions within the ear. Soluble carbohydrates, spike, spikelet, fertility, grain number     

Grain number determination in durum wheat as affected by drought stress: An analysis at spike and spikelet level

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.     

Development and Floret Survival in Wheat Ears With Supernumerary Spikelets

In the supernumerary spikelet wheat, AUS159I0, the supernumeraryspikelet primordia appeared just after the ear reached the terminalspikelet stage. Appearance of the primordia of the multiplesessile spikelets preceded that of indeterminate rachilla spikelets.Supernumerary spikelets had a lower number of potentially fertileflorets per spikelet than normal (non-supernumerary) spikeletsin the ear and thus a smaller number of grains per spikelet.Mean weight per grain in the supernumerary spikelet wheat waslower than in the cultivar, Meering, without supernumerary spikelets.Total grain number in the supernumerary spikelet ear was greaterthan in the normal ear despite the lower spikelet fertilityin the former. Within the supernumerary spikelet ear the multiplesessile spikelets had a higher number of grains per spikeletand mean weight per grain than the indeterminate rachilla spikelets.It appears possible to improve the productivity of the supernumeraryspikelet ear by breeding for reduced expression of the indeterminaterachilla spikelets. Wheat, ear development, floret survival, supernumerary spikelets, grain number     

Characterization and mapping of a Prbs gene controlling spike development in Hordeum vulgare L.

The barley mutant, poly-row-and-branched spike (prbs) showed altered inflorescence morphology: complete conversion of the rudimentary lateral spikelets in two-rowed barley into fully developed fertile spikelets similar to the six-rowed phenotype, and additional spikelets in the middle of spike. Moreover, branched spikes emerged in progeny from a cross between the mutant and a six-rowed barley cultivar. Morphological observation of the development of immature spikes of the mutant and descendants with branched spikes showed that the Prbs gene is involved in spikelet development in the triple-mound stage. In mutant prbs, new meristems initiated at the flanks of lateral spikelets and middle spikelet meristems were converted to branch meristems, developing branched spikes. These observations suggested that the Prbs gene plays a crucial role in spikelet initiation and identity maintenance. The Prbs gene may be an important modifier in inflorescence differentiation from a panicle into a spike. The branched spikes emerging in hybrids from a cross between the mutant and six-rowed barley cultivar were not conferred by the gene vrs1 or Int-c, which decide spike morphology in six-rowed barley. These results imply that although six-row genes vrs1 and Int-c and prbs have similar effects on lateral spikelet development, they have different functions in branched spikes. The Prbs gene was mapped to chromosome 3H between SSR marker Bmag0023 and marker Cbic60 at a genetic distance of 3.3 and 5.4 centimorgans (cM), respectively.     

A genome-wide associate study reveals favorable alleles conferring apical and basal spikelet fertility in wheat (<Emphasis Type="Italic">Triticum aestivum</Emphasis> L.)

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.