Photosynthesis and transpiration of the flag leaf in four spring-wheat cultivars

Co₂ exchange and transpiration rates of the flag leaves of four spring wheat (Triticum aestivum L.) cultivars, namely Glenlea, Neepawa, Opal and Kolibri, were compared using infra-red gas-analysis technique. The plants were grown in a controlled environment under an 18-h photoperiod, with day and night temperatures of 20 and 15° C, respectively. The time course of the CO₂-exchange rate (CER) of the flag leaf differed among cultivars. CER began to decrease rapidly some 2 weeks after ear emergence in Glenlea, Neepawa and Kolibri, but only after 4 weeks in Opal. The decline in CER of Glenlea, Neepawa and Opal was continuous throughout the period of grain development whereas in Kolibri CER was maintained at a constant level between the 4th and 6th weeks after ear emergence. The transpiration rates of the flag leaves of the 4 cultivars did not change markedly until 6–7 weeks after ear emergence, indicating that the reduction in CER was not primarily a response to increased stomatal resistance to the diffusion of CO₂. Removing the ear of the main shoot of intact plants failed to depress CER of the subtending flag leaf until 5 weeks after ear removal. Removing the ears of all the tillers of plants in which all but 3 tillers had been removed at ear emergence did not depress CER until 4 weeks after ear emergence, but removal of the ear of the main shoot of plants where all the tillers had been removed at ear emergence reduced the CER of the flag leaf 2 weeks after ear removal. Removal of tillers at ear emergence had a marked effect on the time course of CER and transpiration rates of the flag leaf. Both CER and transpiration rates of a 4-tiller plant were maintained at a higher level throughout ear development as compared to those of a one-tiller plant. The transpiration rate of the flag leaf of Glenlea increased during the later part of the life of the leaf even for one-tiller plants with no ear, indicating that such a stomatal response may be part of the normal course of leaf aging and not a response to a feedback stimulus from the ear.     

Studies in the Physiology of Flowering of Timothy (Phleum pratense L.): IV. Effect of Shoot Age and Nitrogen Level on the Size of the Inflorescence

The main-stem ear lengths of S. 48 timothy plants increasedwith shoot age at the time of flowering, reaching a peak afterthe expansion of 20–25 leaves and then declining again:similar responses were also apparent in subsidiary tillers onthe same plants. In natural conditions, the maximum ear lengthswere attained on shoots originating in autumn and early winterand flowering the following summer; shoots arising later developedprogressively shorter ears. It is suggested that the potentialear length attainable on a shoot is linked with the size ofthe shoot apex built up during vegetative development. In early formed tillers, mainly primary and secondary, a reducednitrogen supply decreased the size of ears by limiting spikedifferentiation. The intensity of the nitrogen effect increasedin later generations of tillers, with the result that the influenceof shoot age on ear length became obscured. The results emphasizedthe importance of the internal relations between tillers inperennial plants, especially with regard to mineral nutrition.     

Temperature controls seed germination and dormancy in the European woodland herbaceous perennial Erythronium dens-canis (Liliaceae)

We examined the germination ecology and the temperature requirements for germination of Erythronium dens-canis, under both outdoor and laboratory conditions. E. dens-canis is a spring flowering woodland geophyte widely distributed across Europe. Germination phenology, including embryo development and radicle and cotyledon emergence, were investigated in a natural population growing in Northern Italy. Immediately after harvest, seeds of E. dens-canis were either sown on agar in the laboratory under simulated seasonal temperatures or placed in nylon mesh sachets and buried in the wild. Embryos, undifferentiated at the time of seed dispersal, grew during summer and autumn conditions in the laboratory and in the wild, culminating in radicle emergence in winter when temperatures fell to ≈ 5 °C. Emergence of cotyledons did not occur immediately after radicle emergence, but was delayed until the end of winter. Laboratory experiments showed that temperature is the main factor controlling dormancy and germination, with seeds becoming non-dormant only when given warmth, followed by cold stratification. Unlike seeds of E. dens-canis that germinate in winter, in other Erythronium species radicle emergence occurs in autumn, while in some it is delayed until seeds are transferred from winter to spring conditions. Our results suggest that there is genetic and environmental control of the expression of seed dormancy amongst Erythronium species, which is related to local climate.     

Uptake and distribution of nitrogen in wheat plants supplied with different amounts of nitrogen after stem elongation

The uptake of nitrogen and its distribution between shoots and between organs within shoots in wheat (Triticum aestivum) was studied from the start of stem elongation to 28 days after anthesis in a glasshouse experiment with eight nitrogen levels between 0·1 and 12·8 mequiv./litre. There was no net uptake of nitrogen in plants supplied with 0·8 mequiv./litre or less; with more nitrogen the absorption increased linearly. Twenty to 44% of the total plant nitrogen was absorbed after anthesis, this fraction increasing with nutrient supply. The nitrogen allotted to the main shoot decreased until the onset of anthesis and increased thereafter at the expense of the tillers, except with 12·8 mequiv./litre, where nitrogen percentage in the main shoot decreased also after anthesis. Raising nitrogen supply increased the proportion of plant nitrogen recovered in the tillers. Nitrogen accumulated in the ear after emergence and by the 28th day after anthesis it contained between 52% and 73% of the total plant nitrogen. The ear of the main shoot had a higher proportion of shoot nitrogen than that of the tillers. The fraction of ear nitrogen supplied by retranslocation decreased from almost 100% with 0·8 mequiv. N/litre or less to nil with 12·8 mequiv./litre. Increasing nitrogen application decreased the fraction of total nitrogen allocated to the ear.     

Growth and development of Potamogeton distinctus in an irrigation pond in SW Japan

Growth and development of a population of Potamogeton distinctus were studied over one vegetation period.
The morphological structure of the species is described. Maximum development of the size of shoot complexes occurred in August (up to 12 g dry weight/shoot complex). The plant exhibits a regular growth cycle with continuous horizontal and vertical growth that is illustrated by the development of horizontal shoots, vertical shoots and different plant parts. The lower horizontal shoots allow an extension up to 1.8 m from the point of germination. Before the rainy season in June the 1st to 5th generations of vertical shoots mainly contribute to the standing crop of the plants' stand, and after the rainy season the 5th to 9th generation shoots are predominant. Floating leaves make up the main proportion of biomass during the whole growth cycle. Almost 100% of the shoot complexes were found flowering and producing numerous seeds. Up to 16% of the standing crop are allocated to inflorescence and seeds in August. Turions failed to form that year because of rapid desiccation of the habitat. The observed average lifetime of a vertical shoot is appr. 65 days, the estimated turnover rate is between 2.15 and 2.27.     

Effect of Succinic Acid-2,2-Dimethylhydrazide on Endogenous Auxin Level in Apple Shoots

Endogenous auxin levels in the shoots of apple cv. Ingrid Marie (red mutant) treated with SADH (succinic acid-2,2-dimethylhydrazide) were measured. SADH was applied in aqueous solution at 12.5, 25 or 50 mM concentrations in June, 3 weeks after flowering. The defoliated shoot tips were analysed just before SADH spray and 7, 15, 30 and 60 days after spraying. Similar treatments had been made in earlier years. When analysed before the treatment of the year started, shoot extracts of control plants contained higher auxin level than those shoots which were to receive SADH treatment, indicating a residual effect of SADH treatmens during previous years. There was almost no auxin activity in the shoots analysed after 7, 15 and 30 days of SADH treatment. The control plants maintained a high level of auxin activity during this period. However, after 60 days of treatment, shoots treated with 25 or 50 mM exhibited higher auxin activity than control shoots. There appears to be no relationship between the SADH concentration and reduction in auxin activity in the shoots at early stages after treatment.     

Aa TFL1 confers an age-dependent response to vernalization in perennial Arabis alpina

Flowering of many plants is induced by environmental signals, but these responses can depend on the age of the plant. Exposure of Arabidopsis thaliana to vernalization (winter temperatures) at germination induces flowering, whereas a close perennial relative Arabis alpina only responds if exposed when at least 5 weeks old. We show that vernalization of these older A. alpina plants reduces expression of the floral repressor PEP1 and activates the orthologs of the Arabidopsis flowering genes SOC1 (Aa SOC1) and LFY (Aa LFY). By contrast, when younger plants are vernalized, PEP1 and Aa SOC1 mRNA levels change as in older plants, but Aa LFY is not expressed. We demonstrate that A. alpina TFL1 (Aa TFL1) blocks flowering and prevents Aa LFY expression when young plants are exposed to vernalization. In addition, in older plants, Aa TFL1 increases the duration of vernalization required for Aa LFY expression and flowering. Aa TFL1 has similar functions in axillary shoots, thus ensuring that following a flowering episode vegetative branches are maintained to continue the perennial life cycle. We propose that Aa TFL1 blocks flowering of young plants exposed to vernalization by setting a threshold for a flowering pathway that is increased in activity as the shoot ages, thus contributing to several perennial traits.     

Analysis of quantitative traits connected with seed weight and flowering terms in birdsfoot trefoil (Lotus corniculatus L.) plants

The nature of inheritance of characters connected with the seed size (seed mass) and quality of the shoots (germination energy, seed viability, general shoot length, shoot mass, dry weight of shoots) in Lotus corniculatus L. was analyzed. The investigations were carried out on plants of three varieties: the wild form from the Krasnodar Region and local forms MF1 and MF3. The correlation analysis was carried out. The pattern of inheritance in the terms of plant flowering and length of shoots were studied.     

EFFECTS OF AGE AND SIZE ON LIFE HISTORIES AND POPULATION GROWTH OF RHODODENDRON MAXIMUM SHOOTS

Age- and size-specific shoot life histories were studied with population censuses in June 1984 and June 1985 in an evergreen understory shrub. Rhododendron maximum. Most shoots (65%) survived without branching or flowering, and lesser numbers branched (2%), flowered (20%), or died (23%) during the year between censuses. The probabilities of surviving, branching, flowering or dying were both age- and size-dependent. Small, young shoots increased in leaf area. Flowering occurred most prominently in 3- to 6-year old shoots that had exceeded a leaf area of 200 cm², and the rate of flowering increased proportionately with size above this threshold. Branching normally occurred in the year following flowering. The age and size distributions of the population shifted significantly between years, indicating a nonequilibrium population. The survival schedule was Deevey Type I, indicating a high degree of “parental care” of young shoots. Age- and age + size-based demographic models predicted a rapid decline of the shoot population over a decade, while a size-based model predicted a much slower decline in shoot numbers. A sensitivity analysis of the models showed that overall shoot population growth was positively influenced by branching shoots and shoots that added leaf area, and negatively influenced by shoots that lost leaf area, died, or flowered. The role of shoot life histories in determining individual plant fitness and ecological dominance is discussed.     

Relationship between reproductive behavior and new shoot development in 5-year-old branches of olive trees (Olea europaea L.)

The development of new shoots plays a central role in the complex interactions determining vegetative and reproductive growth in woody plants. To explore this role we evaluated the new shoots in the olive tree, Olea europaea L., and the effect of fruiting on new shoot growth and subsequent flowering. Five-year-old branches served as canopy subunits in order to obtain a global, whole-tree view of new shoot number, size and morphological origin. The non-bearing trees had many more shoots than the fruit-bearing trees, and a greater number of longer shoots. In both bearing conditions, however, the majority of shoots were less than 4 cm long, with shoots of progressively longer lengths present in successively decreasing frequencies. Six major shoot types were defined on the basis of apical or lateral bud origin and of parent shoot age. On fruit-bearing trees, the new shoots originated predominantly from the shoot apex, while on non-fruiting trees, they formed mainly from axillary buds, but in both cases, they tended to develop on younger parent shoots. The previous bearing condition of the tree was the main determinant for subsequent inflorescence development, which was independent of both shoot type and length. Thus, reproductive behavior strongly affected both the amount and type of new branching, but subsequent flowering level was more influenced by previous bearing than by the potential flowering sites on new shoots.     

Survival of Tillers and Distribution of Dry Matter between Ear and Shoot of Barley Varieties

Plants of Plumage Archer barley grown in pots produced moreshoots than did Proctor, but had fewer ears at maturity, becausesome shoots died about 7 days before ear emergence. The numberand position on the plant of the shoots that died were consistentfor particular growing conditions. Shoots that died were notalways the last to be produced. There were no consistent differencesin dry weight, leaf area, nitrogen content, or apex developmentbetween shoots that did and did not survive; nor did removingthree developing ears on older shoots affect the survival ofother shoots. Growth of Plumage Archer plants was not checkedby death of shoots; dry matter, nitrogen, and leaf area wereredistributed so that increase in surviving shoots compensatedfor losses in the dead shoots. The dry-weight ratio of ear to shoot was smaller for Proctorthan for Plumage Archer at ear emergence and anthesis, but atmaturity it was greater for Proctor, both when ears were shadedto prevent them photosynthesizing and when they were unshaded.The varietal difference in ear: shoot dry-weight ratio was reversedbecause the relative growth-rate of ears of Proctor was greaterand because more dry matter was lost from its shoots. Both changesmay have been caused by translocation to the ear of a greaterproportion of the assimilate from the shoots of Proctor thanof Plumage Archer. Leaves of Proctor appeared to be more efficientin producing dry matter for the ear than those of Plumage Archer.     

Management of below-ground biomass of <Emphasis Type="Italic">Typha angustifolia</Emphasis> by harvesting shoots above the water surface on different summer days

A dynamic model of regrowth in Typha angustifolia after cutting shoots above the water surface was formulated by characterizing the phenology and mobilization of resources from below-ground to above-ground organs after the cutting. The model parameters were determined by two cutting experiments to investigate the different strategies with flowering and non-flowering shoots after cutting in 2001 and by four cutting experiments to elucidate the regrowth characteristics after cutting on different days from June to September in 2002. A difference was evident both for flowering and non-flowering shoots and for each cutting day. From June to August, non-flowering shoots regrew immediately after cutting, but flowering shoots did not. The shoot regrowth height, number of leaves and shoot biomass were higher with the earlier cutting. The model was validated using the below-ground biomass observed in December 2002 and below-ground dynamics observed in 2003. In the low-flowering shoot zone of the stands, in which the percentage of flowering shoots was small (around 10%), the decrease in below-ground biomass became larger from June (20%) to August (60%). Cutting the high-flowering shoot zone (flowering shoots: 78%) in July 2001, just 1 week after peduncle formation, decreased the below-ground biomass by about 50%. In the low-flowering shoot zone, cutting just before senescence is better for decreasing below-ground biomass with a smaller rate of flowering shoots. The difference of below-ground biomass reduction in non-flowering shoots is mainly due to the decrease in downward translocation (DWT) of above-ground material to below-ground organs during senescence, because of the decrease in regrowth biomass. As for flowering shoots, the decrease in the photosynthate transportation from above-ground to below-ground organs and that of DWT are closely related because they cannot grow again within the season.     

THE EMERGENCE AND DEVELOPMENT OF BRANCHES IN CROTALARIA JUNCEA AND THEIR RELATIONSHIP TO FLOWERING

Nanda , K. K. (Forest Res. Inst., Dehra Dun, India.) The emergence and development of branches in Crotalaria juncea and their relationship to flowering. Amer. Jour. Bot. 49(4): 334–341. Illus. 1962.—Seeds of Crotalaria juncea L. were sown in pots on March 23, 1959, and records were kept of the dates of emergence of individual branches and the appearance of flower buds on them. Periodical observations were also made of the height of the main shoot as well as its branches and the number of nodes and leaves borne by them throughout the year. The main shoot elongates rapidly and terminates in an inflorescence. Development of lateral buds remains completely arrested during the period of rapid elongation and is initiated only after the appearance of the floral buds when it takes place in basipetal sequence. The flowering of the branches also takes place in a basipetal manner. This mode of emergence of branches and their flowering are exhibited even by secondary and tertiary branches. The length attained by these branches is very small as the flower buds appear soon after their emergence. In contrast, the branches formed towards the middle of May continue to elongate for a considerable period and become many times longer than the main shoot or the branches produced earlier in the season. The vegetative period of these branches is also very much prolonged. These differences in the height attained by branches produced at different times of the year and the basipetal sequence in the emergence of branches and their flowering appear to be under the control of some physio-chemical changes which cause the transformation of the growing apex from the vegetative to the reproductive state. This holds good irrespective of whether these changes are brought about as a result of a favorable environmental complex, as is the case with the main shoot and late-formed, much elongated branches, or are due to the favorable internal conditions produced within the plant as a result of the completion of the developmental process of the main shoot, as happens in the case of branches produced earlier in the season.     

Short and long term effects of root and shoot chilling of ransom soybean

The immediate short term effects on some physiological processes and the long term effects on morphology and reproductive development of root- and shoot-chilled soybeans (Glycine max L. cv Ransom) were studied. Roots or shoots of 16- or 17-day-old plants were chilled at 10°C for one week, and then rewarmed to 25°C. Leaf elongation rate, net CO₂ uptake rate, and stomatal conductance decreased during root or shoot chilling. Root chilling had only temporary effects on water relations, while shoot chilling caused large changes in potentials during chilling. Most processes measured returned to control levels after two days of rewarming. Root-chilled plants harvested 90 days after emergence were similar in morphology and seed weight to controls. Shoot-chilled plants showed a large increase over controls in axillary branch growth, but an early abortion of flowers and a delayed resumption of flowering caused a 78% reduction in seed weight. Root chilling in this study was found to have little or no long term effect on the plants, while shoot chilling caused significant changes in vegetative morphology, and a delay in flowering and subsequent pod filling.     

Morphological characteristics of annual Zostera marina shoots at various germination temperatures

The timing of the transition from seed, seedlings and development into flowering is paramount importance in annual-type Zostera marina, because flowering is the first step of sexual reproduction. A majority of plants use environmental cues to regulate the transition to their developmental stages because plants must flower synchronously for successful outcrossing and must complete their sexual reproduction under favorable external conditions. The morphological characteristics (seeds and lateral shoot production, branch number, and inflorescence length) of reproductive shoots of Z. marina L. were examined in outdoor mesocosms to better understand the reproductive strategies of annual populations. Seeds in the germination experiment were divided into two groups: those exposed to cold (7 °C; vernalized group) and those left untreated (25-21 °C; non-vernalized group). All 600 seeds (300 from each group) were cultured for 2 months at 7, 10, 15, 20, and 25 °C in an indoor incubator. In the vernalized group, the germination rates were almost significantly higher than in the non-vernalized group. However, germination rates were not significantly affected by germination temperature. In outdoor mesocosms, production of vegetative shoots was observed in plants germinated at 15 and 20 °C in the vernalized group and at 10, 15 and 20 °C in the non-vernalized group. The highest number of vegetative shoots produced (35) was observed in plants germinated at 20 °C in the vernalized group, whereas seeds of either group failed to produce vegetative shoots when germinated at a low temperature (7 °C).In the flowering phase, the number of branches per shoot in the vernalized group was significantly higher than in the non-vernalized group. The total number of spadices on the 1st branches of plants in the vernalized group (germination at 20 °C) was significantly lower than that in the non-vernalized group at the same germination temperature. The total number of spadices per reproductive shoot in the vernalized group (germination at 10 °C) was also higher than in the non-vernalized group. Thus, both low temperature (vernalization) and seed germination temperature have implications for the sexual and asexual propagation of annual Z. marina populations.     

Ecophysiology of embryo development and seed germination of the European woodland herbaceous perennial Corydalis cava (L.) Schweigg. & Körte subsp. cava (Fumariaceae)

In this study we examined the germination ecology with special reference to the temperature requirements for embryo development and germination of Corydalis cava subsp. cava, under both outdoor and laboratory conditions. Corydalis cava is a spring flowering woodland tuberous geophyte widely distributed across Europe. Germination phenology, including embryo development and radicle and cotyledon emergence, was investigated in a population growing in northern Italy. Immediately after harvest, seeds of C. cava were sown both in the laboratory under simulated seasonal temperatures and naturally. Embryos, undifferentiated at the time of seed dispersal, grew during summer and autumn conditions, culminating in radicle emergence in winter, when temperatures fell to ca 5°C. Cotyledon emergence also occurred at ca 5°C, but first emergence was delayed until late winter and early spring. Laboratory experiments showed that high (summer) followed by medium (autumn) and low temperatures (winter) are needed for physiological dormancy loss, embryo development and germination respectively. Unlike seeds of C. cava that germinated in winter, in other Corydalis species radicle emergence occurred in autumn (C. flavula) or did not depend on a period of high summer temperature to break dormancy (C. solida). Our results suggest that subtle differences in dormancy and germination behavior between Corydalis species could be related to differences in their geographical distribution.     

<Emphasis Type="Italic">In vitro</Emphasis> germination and axillary shoot propagation of <Emphasis Type="Italic">Centaurea zeybekii</Emphasis>

In vitro culture is an important aid for ex situ conservation of rare, endemic or threatened plants. In this work, we establish an efficient method for the seed germination, seedling development, and axillary shoot propagation of Centaurea zeybekii Wagenitz. The seeds, collected from a wild population, were surface sterilised and cultured on various in vitro germination media. The effects of photoperiod and temperature on seed germination were also investigated. Germinations were obtained after 6 weeks in culture and the radicle emergence was evaluated as a main indicator. A high frequency of germination was obtained on distilled water supplemented with vitamines and 1 mg/L GA₃. Although the seed germination frequencies were not affected by photoperiod, the highest germination frequency was obtained at 24 ± 2°C. A high frequency of axillary shoot proliferation was produced on MS medium supplemented with 1 mg/L BA. Then, the axillary shoots were separated and transferred to MS medium with or without plant growth regulators for rooting. Rhizogenezis was promoted after 6 weeks only in MS and 1/2 MS media containing 0.5 mg/L IBA. The rooting process was very slow and the percentage of shoot rooting was also very low (15%). The present study not only enables reinforcement of wild plant populations using ex situ growth of individuals, but it also helps to large number of aseptic seedling to use it in clonaly micropropagation studies.     

Growth patterns of Juncus gerardi clonal populations in a coastal habitat

Juncus gerardi populations demonstrated a logistic growth curve during the colonization stage. Shoot production by vegetative multiplication was virtually continuous from December to June. Experiments suggested that the stabilisation stage of the demographic curve reflected water deficit. Taller, fertile, winter and early spring cohorts could be distinguished from shorter, infertile end of spring and beginning of summer cohorts. Shoot emergence began in March and terminated at the end of June, when water becomes a limiting factor due to a period of water shortage, typical of the thermo-atlantic climate. Spatial extension of populations was due to rhizome growth, which ceased during flowering.Flowering in May temporarily checked growth in shoot height of all emerged cohorts. No cost of reproduction was demonstrated concerning the rate of appearance of new shoots.Although fertile shoots were taller than vegetative shoots, their growth rates were significantly lower from April onwards. The tallest fertile shoots produced the most capsules.Energy allocation to seed production is the only possible means for long-term establishment of new genotypes, and vegetative multiplication appears as the principal source of recruitment of new modules in Juncus gerardi.Resource allocation patterns in this clonal species are discussed in relation to the ecological background in the concerned marshlands and with theoretical proposals derived from models of spatial colonization strategies in clonal plants.Nomenclature: follows Flora Europaea (Tutin et al., 1964ndash;1980).     

Effect of the timing of water deficit on growth, phenology and yield of pearl millet (Pennisetum glaucum (L.) R. Br.) grown in Sahelian conditions

Several studies conducted under high input conditions have indicatedlittle susceptibility of pearl millet to water deficit untillearly grain filling, because the losses in main shoot productionwere fully compensated by increased tiller fertility. The presentstudy assessed the impact of water deficits at three developmentstages: prior to flowering (S30), at the beginning of flowering(S45), and at the end of flowering (S60) in pearl millet grownin experimental conditions similar to Sahelian farming conditions.It included a control irrigation treatment simulating the naturaldistribution of rainfall throughout the cropping season. Bothbiomass production and grain yield were severely reduced byS30 and S45, while S60 had no effect. In S30 and S45, the floweringof tillers was delayed or totally inhibited. In both of thesetreatments, the low number of productive tillers did not compensatefor damage to panicle initiation and flowering of the main shoot.All treatments maintained green leaves on the main shoot duringthe grain filling period, and in S30 leaf growth recovered frommid-season drought. These results illustrate how pearl milletmostly escapes drought by matching its phenology to the meanrainfall distribution in the Sahel. In the case of mid-seasondrought, some late productive tillers and the maintenance ofgreen leaf biomass of the main shoots limited, but did not overcome,the yield losses. This study stresses the importance of agro-ecologicalconditions in control treatments, particularly the water regimeand crop density, when assessing crop drought resistance. Key words: Drought resistance strategy, experimental conditions, main shoots, tillers, Pennisetum glaucum     

Wheat bulb fly, Leptohylemyia coarctata Fall., and its effect on the growth and yield of wheat

In two experiments done in successive years to compare the growth and yield of Cappelle wheat either protected from or exposed to attacks by larvae of wheat bulb fly, the plots were previously fallowed, but egg laying was prevented on half of each plot by using Polythene soil covers. In the first season wheat was sown at the end of October, November and December and in the second season in late October and in early January, when there were two sowings, one with and one without a spring application of herbicide. The infestation rate was 1·1-1·7 million eggs per acre, typical of a moderate attack. Larvae had little effect on the yield of October-sown wheat as the plants had two shoots each when first attacked and few were killed. On plots sown late, yield was decreased by up to 22%, as plants had only a single shoot when attacked and many were killed. The main effect of wheat bulb fly was to reduce the number of ear-bearing shoots by killing plants and restricting the production of new shoots. Surviving plants partially compensated by producing more ear-bearing shoots with heavier ears and slightly heavier seeds than normal. Killed plants were not distributed uniformly but were often in patches several feet across. Wheat on the attacked plots ripened more slowly and unevenly than on the unattacked plots. Weather affects the growth of the plants and activity of the larvae and thus partly determines percentage shoot survival.