Phyllotaxis in the Oil Palm: Arrangement of Male/Female Spikelets on the Inflorescence Stalk

The geometry of spikelet arrangement along the massive maleand female inflorescences of this monoecious palm is investigatedthrough techniques of phyllotaxis measurement (Equivalent phyllotaxisindex or E.P.I. Essentially there is little apparent differencewhether E.P.I. values from male inflorescences or female areconsidered. In both sexes E.P.I. estimates vary in a curvilinearmanner along the inflorescence length, higher values being obtainedtoward the broad base. Based on this pattern one value-over-allinflorescence E.P.I. is suggested to compare bunches emanatingfrom different treatment or genetic sources. It is also shownthat over-all bunch (inflorescence) E.P.I. varies systematicallywith palm age, being low in young palms and rising to asymptoticlevels in c. 11-year-old palms. Some physiological explanationsfor this latter observation are put forward, and some possibleapplications in cultural and genetic studies are suggested.Attention is also given to describing the results in terms ofFibonacci contact parastichy systems.     

Phyllotaxis in the Oil Palm: Application in the Evaluation of pisiferas

Yield differences between and within four segregating familiesof Oil Palm are shown to be highly correlated with differencesin the phyllotaxis index, E.P.I., of the female inflorescences.This association should facilitate prediction of the yield potentialof an effectively sterile segregant palm type known as pisifera,which is used as a male parent in hybrid seed production.     

Spikelet structure and development in Cyperoideae (Cyperaceae): a monopodial general model based on ontogenetic evidence

Background and Aims

In Cyperoideae, one of the two subfamilies in Cyperaceae, unresolved homology questions about spikelets remained. This was particularly the case in taxa with distichously organized spikelets and in Cariceae, a tribe with complex compound inflorescences comprising male (co)florescences and deciduous female single-flowered lateral spikelets. Using ontogenetic techniques, a wide range of taxa were investigated, including some controversial ones, in order to find morphological arguments to understand the nature of the spikelet in Cyperoideae. This paper presents a review of both new ontogenetic data and current knowledge, discussing a cyperoid, general, monopodial spikelet model.

Methods

Scanning electron microscopy and light microscopy were used to examine spikelets of 106 species from 33 cyperoid genera.

Results

Ontogenetic data presented allow a consistent cyperoid spikelet model to be defined. Scanning and light microscopic images in controversial taxa such as Schoenus nigricans, Cariceae and Cypereae are interpreted accordingly.

Conclusions

Spikelets in all species studied consist of an indeterminate rachilla, and one to many spirally to distichously arranged glumes, each subtending a flower or empty. Lateral spikelets are subtended by a bract and have a spikelet prophyll. In distichously organized spikelets, combined concaulescence of the flowers and epicaulescence (a newly defined metatopic displacement) of the glumes has caused interpretational controversy in the past. In Cariceae, the male (co)florescences are terminal spikelets. Female single-flowered spikelets are positioned proximally on the rachis. To explain both this and the secondary spikelets in some Cypereae, the existence of an ontogenetic switch determining the development of a primordium into flower, or lateral axis is postulated.     

Understanding spikelet orientation in Paniceae (Poaceae)

Spikelet structure and grouping are key characters to identify grasses. Here we tested the possibility that spikelet pairs, a distinctive morphological structure of many Andropogoneae and Paniceae, are the starting point for a secondary single spikelet condition that can also explain the change of spikelet orientation among Paniceae genera. As a first approach, we studied the inflorescence development of Paspalum simplex, P. stellatum, and Axonopus sufultus to clarify the origin of the spikelet orientation and other basic homologies. The results support that solitary spikelets of A. suffultus are homologous to the subsessile spikelets of P. simplex and that solitary spikelets of P. stellatum are homologous to the pedicellate spikelet of P. simplex. This last homology supports that spikelet orientation results from a differential reduction/abortion of either the pedicellate or the subsessile spikelet primordia. We also discuss the possibility that the RAMOSA and polar auxin pathways could play a role in the abortion of the lateral subsessile spikelets in P. stellatum. However, the apical meristem inhibition observed in A. suffultus and P. stellatum seems to depend on a very different genetic control, suggesting that the single spikelet condition is homoplasic within Paniceae and derived from at least two different genetic mechanisms.     

The indeterminate floral apex1 gene regulates meristem determinacy and identity in the maize inflorescence

Meristems may be determinate or indeterminate. In maize, the indeterminate inflorescence meristem produces three types of determinate meristems: spikelet pair, spikelet and floral meristems. These meristems are defined by their position and their products. We have discovered a gene in maize, indeterminate floral apex1 (ifa1) that regulates meristem determinacy. The defect found in ifa1 mutants is specific to meristems and does not affect lateral organs. In ifa1 mutants, the determinate meristems become less determinate. The spikelet pair meristem initiates more than a pair of spikelets and the spikelet meristem initiates more than the normal two flowers. The floral meristem initiates all organs correctly, but the ovule primordium, the terminal product of the floral meristem, enlarges and proliferates, expressing both meristem and ovule marker genes. A role for ifa1 in meristem identity in addition to meristem determinacy was revealed by double mutant analysis. In zea agamous1 (zag1) ifa1 double mutants, the female floral meristem converts to a branch meristem whereas the male floral meristem converts to a spikelet meristem. In indeterminate spikelet1 (ids1) ifa1 double mutants, female spikelet meristems convert to branch meristems and male spikelet meristems convert to spikelet pair meristems. The double mutant phenotypes suggest that the specification of meristems in the maize inflorescence involves distinct steps in an integrated process.     

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     

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。     

Sympodial structure of spikelets in the tribe Schoeneae (Cyperaceae)

Spikelet morphology of 250 specimens of 47 species of Schoeneae was examined using light microscopy and scanning electron microscopy. We confirmed that spikelet structure in Schoeneae is cymose with a sympodial "rachilla." Monopodial spikelets, as described by most current literature, were not found in Schoeneae. Prophylls are not always present in sympodial spikelets and cannot be used to determine whether a spikelet is sympodial or monopodial. Spikelets of Schoeneae develop acropetally, and the uppermost glume may or may not produce a flower. The last feature may be variable within species and within individual plants, so presence or absence of this flower is not an indication of sympodial or monopodial spikelet structure in Schoeneae. Relative position of flower, glume, and axis is a reliable criterion to judge whether spikelets are sympodial or monopodial. In some species of Schoenus and in Ptilothrix, formation of the arch-shaped base of the fertile glume relates to the shape of the inclined nodes on which the glume grows. This study highlights the need to reinvestigate spikelet structure in other tribes of Cyperaceae.     

Development of the mixed inflorescence in Zea diploperennis litis, Doebley & Guzman (Poaceae)

Development of the mixed inflorescence in Zea diploperennis Iltis, Doebley & Guzman (Poaceae) Mixed inflorescences of diploperennial teosinte, which terminate the main branches of the plant, arise in the same fashion as tassel spikes. The apical meristem produces bracts in a decussate arrangement. A single axillary bud primordium is initiated in the axil of each bract. Growth of the bract is retarded as the bud enlarges and divides longitudinally into two separate spikelet primordia. The paired spikelets running in two ranks on either side of the inflorescence primordium produce the four-rowed condition typical of teosinte tasselS. In the transition region between male and female portions of the inflorescence, development of the pedicellate spikelet of each spikelet pair is arrested at an early ontogenetic stage. Continued growth of the sessile spikelet and associated rachis flaps destroy the remnants of the arrested spikelet in basal portions of the inflorescence. A similar abortion of the lower floret of the sessile spikelet results in a single pistillate floret per node at anthesis. These results provide further support for the hypothesis that a tassel-like mixed inflorescence of teosinte is ancestral to the maize ear.     

苔草属植物的返祖两性小穗

本文报告了大别苔(Carex dabiecnsis)和白鳞苔草(C.polyschoena)的返祖小穗。这些返祖小穗中的类型之一具有与篙草属(Kobresia)以及Schoenoxiphium属完全相似的两性结构小穗,在这一类型的小穗中,它们生有一雌花及其在上的雄花。如图所示,大别苔和白鳞苔草中第(3)类型的返祖小穗和Schoenoxiphium属以及嵩草属的第1、2类型的小穗基本上没有区别,这些返祖小穗的发现证明果胞是苔草属的真正小穗,而且可以证明现存苔草的单性小穗是起源于具两性小穗的祖先。因此,可以相信具有两性结构的返祖小穗的发现进一步揭示了苔草亚科中Schoenoxiphium属,蒿草属,钩轴莎属和苔草属之间的系统发育的亲缘关系。     

A Study of Floret Development in Wheat (Triticum aestivum L.)

Plants of wheat (Triticum aestlvum L.) cv. Aotea were grownat high or low nitrogen levels and in a natural photoperiodor continuous light. Starting 17–21 days from the double-ridgestage, eight plants from each treatment were sampled every 3days until anthesis, and the two basal, the sixth, and the terminalspikelets were sectioned longitudinally. A developmental scorewas assigned to each floret and rates of development calculated.Continuous light hastened development but reduced the numberof spikelets per ear, while high nitrogen delayed developmentbut increased spikelet numbers. The number of florets initiatedin each spikelet varied within narrow limits, but grain settingdepended strongly on spikelet position and on treatment. Althoughflorets were initiated in acropetal succession, the rate ofdevelopment tended to increase up to floret 4 but then declinedmarkedly. As a result grain setting was confined to basal floretpositions, although the two basal spikelets developed so slowlythat they contributed relatively little to grain yield. Distalflorets degenerated almost simultaneously at or before ear emergence,but those in intermediate positions continued to develop untilafter fertilization in the lower florets. It is argued thatthe spikelet is an integrated system in which correlative mechanismsplay a part throughout the development of the florets.     

Combinatorial control of meristem identity in maize inflorescences

The architecture of maize inflorescences, the male tassel and the female ear, is defined by a series of reiterative branching events. The inflorescence meristem initiates spikelet pair meristems. These in turn initiate spikelet meristems which finally produce the floret meristems. After initiating one meristem, the spikelet pair and spikelet meristem convert into spikelet and floret meristems, respectively. The phenotype of reversed germ orientation1 (rgo1) mutants is the production of an increased number of floret meristems by each spikelet meristem. The visible phenotypes include increased numbers of flowers in tassel and ear spikelets, disrupted rowing in the ear, fused kernels, and kernels with embryos facing the base of the ear, the opposite orientation observed in wild-type ears. rgo1 behaves as single recessive mutant. indeterminate spikelet1 (ids1) is an unlinked recessive mutant that has a similar phenotype to rgo1. Plants heterozygous for both rgo1 and ids1 exhibit nonallelic noncomplementation; these mutants fail to complement each other. Plants homozygous for both mutations have more severe phenotypes than either of the single mutants; the progression of meristem identities is retarded and sometimes even reversed. In addition, in rgo1; ids1 double mutants extra branching is observed in spikelet pair meristems, a meristem that is not affected by mutants of either gene individually. These data suggest a model for control of meristem identity and determinacy in which the progress through meristem identities is mediated by a dosage-sensitive pathway. This pathway is combinatorially controlled by at least two genes that have overlapping functions.     

Floral development and the formation of unisexual spikelets in the Andropogoneae (Poaceae)

We investigated spikelet development in four distantly related species of the grass tribe Andropogoneae to determine whether spikelet development and the formation of unisexual florets are uniform throughout the tribe. We studied development in Bothriochloa bladhii, Coelorachis aurita, Heteropogon contortus, and Hyparrhenia hirta, and compared these with Panicum, a member of the sister tribe Paniceae. Many aspects of spikelet development in the species we have studied correlate with what is already known for Tripsacum and maize (both Andropogoneae), despite variation in how unisexual florets are distributed on the plant. The formation of unisexual spikelets is also uniform. All florets initiate both pistil and stamen primordia. In florets destined to be male, cell death occurs in the subepidermal layers of the gynoecium after the formation of a gynoecial ridge. In florets destined to be female, there is no apparent cell death in the stamens, but growth ceases after anther formation. The similarity in spikelet development and the formation of unisexual florets point to a common genetic mechanism for sex determination throughout the Andropogoneae and possibly the entire Panicoideae. Use of a cell death pathway to cause gynoecial abortion may be the basis of one morphological character that defines the subfamily.     

Inflorescence development in a new teosinte: Zea nicaraguensis (Poaceae)

Inflorescence development in a newly discovered teosinte, Zea nicaraguensis (Poaceae), from Nicaragua has been investigated using scanning electron microscopy (SEM). The SEM examination revealed that the pattern of both male and female inflorescence development was similar to previously described inflorescence in other Zea taxa. Branch primordia were initiated acropetally in a distichous pattern along the rachis of male and female inflorescences. Spikelet pair primordia bifurcated into pedicellate and sessile spikelet primordia. Predictably, pedicellate spikelet development was arrested and aborted in the female teosinte inflorescence. Organogenesis of functional spikelets and florets was similar to that previously described in maize and teosintes. The results were consistent with our hypothesis that both femininity and masculinity share a common mechanism of inflorescence development in Zea and Tripsacum and are in accord with a putative common mechanism of sex determination in the Andropogoneae. Interestingly, this population of teosinte, unique in its ability to grow in water-logged soils, showed a stable pattern of early inflorescence development. Our results also revealed the uncharacteristic presence of inflorescence polystichy in this population of Zea nicaraguensis. We propose this novel phenotypic variation raises the possibility that a domestic evolution of polystichy in maize was enabled by an occasional polystichous phenotypic in teosinte.     

Suppressor of sessile spikelets1 functions in the ramosa pathway controlling meristem determinacy in maize

The spikelet, which is a short branch bearing the florets, is the fundamental unit of grass inflorescence architecture. In most grasses, spikelets are borne singly on the inflorescence. However, paired spikelets are characteristic of the Andropogoneae, a tribe of 1,000 species including maize (Zea mays). The Suppressor of sessile spikelets1 (Sos1) mutant of maize produces single instead of paired spikelets in the inflorescence. Therefore, the sos1 gene may have been involved in the evolution of paired spikelets. In this article, we show that Sos1 is a semidominant, antimorph mutation. Sos1 mutants have fewer branches and spikelets for two reasons: (1) fewer spikelet pair meristems are produced due to defects in inflorescence meristem size and (2) the spikelet pair meristems that are produced make one instead of two spikelet meristems. The interaction of Sos1 with the ramosa mutants, which produce more branches and spikelets, was investigated. The results show that Sos1 has an epistatic interaction with ramosa1 (ra1), a synergistic interaction with ra2, and an additive interaction with ra3. Moreover, ra1 mRNA levels are reduced in Sos1 mutants, while ra2 and ra3 mRNA levels are unaffected. Based on these genetic and expression studies, we propose that sos1 functions in the ra1 branch of the ramosa pathway controlling meristem determinacy.     

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.     

Influence of Vernalization and Photoperiod on Supernumerary Spikelet Expression in Wheat

Two tetraploid (Triticum turgidum L.emend gr. turgidum and gr.durum) and five hexaploid wheats (Triticum x aestivum L. emendgr. aestivum) with reported tendencies for ‘branched heads’(supernurnerary spikelets) exhibited variation in its expressionunder different vernalization photoperiod and temperature regimes. Two main types of supernumerary spikelets were identified, multiplesessile spikelets (MSS) with two or more complete spikeletsat a rachis node and indeterminate rachilla spikelets (IRS)with two to 13 spikelets on an extended rachilla. The degree of supernumerary spikelet expression in wheats withvernalization response differed from those without. Short photoperiods(9–14 h) both outdoors and in a glasshouse environment,were more conducive to supernumerary spikelet expression than24 h photoperiod in both environments. The 24 h photoperiodglasshouse environment (higher mean temperatures) was leastconducive to its expression except in lines with a strong vernalizationresponse. The high stability of supernumerary spikelet expression in certaingenotypes in the different environments indicated the feasibilityof incorporating this character in breeding and selecting commercialwheats to increase grain number per head. Triticum, wheat, ear-branching, supernumerary spikelets, vernalization, photoperiod, temperature