Influence of day-length and isolates of Phytophthora infestans on field resistance to late blight of potato

Main and interaction effects of day-length and pathogen isolate on the reaction and expression of field resistance to Phytophthora infestans were analyzed in a sample of standard clones for partial resistance to potato late blight, and in the BCT mapping population derived from a backcross of Solanum berthaultii to Solanum tuberosum. Detached leaves from plants grown in field plots exposed to short- and long day-length conditions were independently inoculated with two P. infestans isolates and incubated in chambers under short- and long photoperiods, respectively. Lesion growth rate (LGR) was used for resistance assessment. Analysis of variance revealed a significant contribution of genotype × isolate × day-length interaction to variation in LGR indicating that field resistance of genotypes to foliar late blight under a given day-length depended on the infecting isolate. An allele segregating from S. berthaultii with opposite effects on foliar resistance to late blight under long- and short day-lengths, respectively, was identified at a quantitative trait locus (QTL) that mapped on chromosome 1. This allele was associated with positive (decreased resistance) and negative (increased resistance) additive effects on LGR, under short- and long day-length conditions, respectively. Disease progress on whole plants inoculated with the same isolate under field conditions validated the direction of its effect in short day-length regimes. The present study suggests the occurrence of an isolate-specific QTL that displays interaction with isolate behavior under contrasting environments, such as those with different day-lengths. This study highlights the importance of exposing genotypes to a highly variable population of the pathogen under contrasting environments when stability to late blight resistance is to be assessed or marker-assisted selection is attempted for the manipulation of quantitative resistance to late blight.     

A greenhouse assay to screen sunflower for resistance to Alternaria helianthi

A greenhouse assay to screen sunflower for resistance to Alternaria helianthi is described. A comparison of conditions led to the following standard conditions being recommended. The first or second pair of leaves of seedling plants at the V8 growth stage are inoculated using inoculum grown on sunflower leaf extract agar for 5–10 days at an inoculum density of 1–2 spores cm² of leaf tissue. A 48 h dew period should be applied to plants covered by a plastic tent. A dew period temperature of 26/26°C night/day and a post-dew period temperature relative to that experienced under local growing conditions should be applied. Lesions are measured 7 days after inoculation, and mean lesion size per plant is calculated. Mean lesion size of lines being tested is expressed as a proportion of the mean lesion size of a susceptible standard included in each screening experiment.     

Floral morphogenesis in Rudbeckia hirta in relation to polyamine concentration

Changes in polyamine concentration in the long day (LD) plant Rudbeckia hirta were examined over the course of floral initiation and development. Plants of R. hirta were grown to maturity under 9h, non-floral-inductive photoperiods. At maturity, half the plants were placed in ambient day length plus a 4- h night interruption. Plants were sampled at 0, 4, 8, 12 or 16 days for polyamine content and floral initiation. Polyamines were extracted from fully expanded leaves and the meristems were examined histologically. In another experiment, polyamines were extracted from the meristems under paired LD and short day (SD) conditions every 2 days from 0 to 22 days. A rise in free polyamines was linked to important cytological events during floral initiation. Free putrescine and spermidine levels increased after 4 LD and continued until 14 to 16 LD when the levels in the meristem began to decline. Events of floral initiation began between 4 and 8 LD with cell proliferation and the start of stem elongation. Initiation was irreversible after 14 to 16 LD, the period when putrescine and spermidine began to decline. After 4 LD, the polyamine level was consistently higher in the photoinduced plants. Our results from this study, using direct histological comparisons of meristematic development and polyamine concentration, clearly demonstrate a correlation of polyamines and flowering.     

Long-day effects on growth and flower initiation of tomato plants in low light

Young tomato plants (cv. Minibelle) were grown in plant growth cabinets in 575 kJ m^-2 (400–700 nm) daily radiation. Plants grown in an 8 h day were then compared with those in which 10% of the radiation was taken from the main 8 h light period and supplied over the next 8 h period. After 41 days from sowing the 16 h day plants had almost twice the dry weight of those in short days and a 55 % greater leaf area. Net assimilation rate, relative growth rate and relative leaf area growth rates were all greater in long days, although the differences in growth diminished with time. The long-day treatment also increased the proportion of dry weight in the leaves, a function which is usually relatively stable in different environments. The beneficial effect of the long days may arise from a reduction in night respiration, or an increase in rate of photosynthesis through the observed increase in chlorophyll content. The 8 h light period resulted in flower initiation one or two nodes lower than the 16 h period so that the cultivar is a quantitative short-day plant.     

Restricted multiplication of potato leafroll virus in resistant potato genotypes

Plants of a range of potato genotypes differing in rating for field resistance to potato leafroll virus (PLRV) were inoculated with the virus by grafting or by aphids (Myzus persicae). Plants of all genotypes tested became infected by each inoculation method and PLRV was detected by ELISA in the upper leaves of all genotypes within 26 days after grafting. Most genotypes with high resistance ratings developed only mild primary and secondary symptoms whereas those with low resistance ratings developed more pronounced symptoms. However, one genotype (G7461(4)) with a high resistance rating was very severely affected. The concentrations attained by PLRV in genotypes with high resistance ratings were only 1–10% of those in genotypes with low resistance ratings. These differences in virus concentration were found in young leaves of plants with primary or secondary infection, whether inoculated by grafting or by aphids and whether grown in the glasshouse or the field. In older leaves, differences in virus concentration between genotypes were at least as pronounced as those in younger leaves. In contrast, PLRV concentration in vascular tissue at the heel end of tubers of plants with primary infection was similar for all the genotypes tested. Although low PLRV concentration was consistently associated with high resistance rating it is not the only form of resistance to PLRV occurring in potato.     

The maryland mammoth allele and rooting both perturb the fate of florally determined apices in Nicotiana tabacum.

The stability of the florally determined state in terminal and axillary buds of two tobacco cultivars was studied. We used Hicks and Hicks Maryland Mammoth, near-isogenic cultivars of Nicotiana tabacum differing at the recessive maryland mammoth locus which confers short-day behavior. The experimental design consisted of growing plants in short-day conditions and subjecting them to three bioassays in long-day conditions: in vitro culture of apices consisting of meristems and three to four leaf primordia; rooting of buds consisting of meristems and 8 to 12 leaves, leaf primordia, and internodes; and release from apical dominance of axillary buds in situ. Cultured terminal and axillary apices expressed floral determination, indicating that meristems can be florally determined. Two lines of evidence indicate that rooting destabilizes an already acquired florally determined state: cultured apices from both axillary and terminal buds produced fewer nodes after excision than homologous buds which were rooted; and a lower percentage of rooted axillary buds from Hicks Maryland Mammoth plants expressed floral determination than did homologous axillary buds grown out in situ in noninductive conditions. Rooted buds from the two genotypes expressed floral determination at different frequencies, but produced abnormal inflorescences at similar frequencies, indicating that roots and the maryland mammoth allele influence common as well as unique processes associated with floral determination.     

Genetic Regulation of Development in Sorghum bicolor: IV. GA(3) Hastens Floral Differentiation but Not Floral Development under Nonfavorable Photoperiods

Sorghum bicolor (L.) Moench lines with genetic differences in photoperiod requirement were planted in the field near Plainview, Texas (about 34° northern latitude) around June 1 and treated with gibberellic acid (GA₃) solutions applied in the apical leaf whorl. GA₃ hastened the date of floral differentiation (initiation). The greatest responses to GA₃ were by 90M and 100M, the latest of the genotypes, for which floral initiation dates were hastened an average of 19.5 and 21.7 days, respectively, for the 4 years beginning in 1980. There were very small differences in dates of anthesis between control and GA₃-treated plants. Microscopic examination of apical meristems collected between the date of floral initiation of GA₃-treated plants and the later date of initiation of control plants revealed: (a) several morphological characteristics of floral differentiation in the apical meristem of treated plants, (b) consistent occurrence of vegetative morphology in control plants, (c) a few meristems from GA₃-treated plants that appeared to be regressing in floral development and thus possibly exhibiting dedifferentiation. Dedifferentiation of prepanicle primordia into leaves would explain the observed equal or greater number of leaves in GA₃-treated plants rather than the expected smaller number. It is apparent that the presence of a morphological differentiated floral meristem in sorghum does not drive subsequent floral development in the absence of inductive photoperiods. This further suggests that initial floral differentiation and subsequent floral development may be controlled separately in sorghum.     

Concentration of virus and ultrastructural changes in oats at various stages of barley yellow dwarf virus infection

Enzyme-linked immunosorbent assay was used to monitor the concentration of barley yellow dwarf virus (BYDV) in roots and leaves of oats inoculated at the 1 - 2 leaf stage and at the 4 - 5 leaf stage, respectively. Virus was detectable 20 h after inoculation in the roots and after 48 h in the leaves of plants inoculated at the 1 - 2 leaf stage. The virus concentration reached a plateau in the roots after 7–8 days, and was 3–4 times higher than in the leaves. In plants inoculated at the 4 - 5 leaf stage virus was detectable in roots and leaves after 3 and 5 days, respectively. The concentration reached a maximum after 10 days in the roots and after 18 days in the leaves; the concentration in the leaves was 2–3 times higher than in the roots. Virus was readily detectable in seeds from infected plants, both fresh and old dried seeds. However, seed transmission could not be demonstrated. Virus-like particles were first observed in phloem cells of roots 4 days after inoculation, but no ultrastructural changes were detected at this stage. After 5–6 days, disintegrated nuclei and virus-induced vesicles were observed in many cells and abnormal production of callose was found after 10 days. Necrotic phloem cells were observed from day 13, shortly after the appearance of external symptoms.     

Leaf growth of white mustard (Sinapis alba) in different environments

Summary The numbers of cells and area of fully expanded leaves were determined on successive leaves of Sinapis alba grown either in 8 hr. photoperiod (vegetative plants) or 16 hr. photoperiod (flowering plants) at a constant temperature of 20°C. In the 8 hr. photoperiod leaf 9 had the greatest area but leaf 12 had most cells. In 16 hr. photperiod leaf 5 had the greatest area but leaf 9 had most cells. The relationship between area and cell number of successive leaves on the main stem fell into 3 distinct phases: in phase (1), cell number increased at a greater rate than leaf area; in phase (2), leaf area decreased while cell number increased; in phase (3), cell number and leaf area decreased proportionally. For an increase in unit area, cell number increased more in 8 hr. than in 16 hr. photoperiod.Using final area and final cell number of successive leaves, by extrapolation the cell number of unit area of primordium has been deduced. Cell number per unit area increased in successive primordia up to a certain node after which it remained constant at succeeding nodes. It was found that in plants grown under different conditions the cell number per unit area in successive primordia increased at a constant logarithmic rate. That is, cells became progressively smaller. It is concluded that changes in cell size of successive primordia are not influenced by the environment but are under internal control.     

Evidence for metabolic turnover of monoterpenes in peppermint

Two types of experimental evidence are presented which suggest that the monoterpenes of peppermint (Mentha piperita L.) are subject to metabolic turnover. In kinetic studies with ¹⁴CO₂, peppermint cuttings rapidly incorporate label into the monoterpenes and then lose most of the label from the monoterpenes, without corresponding changes in the amount of monoterpenes present. When peppermint plants are grown in a controlled environment (16-hr photoperiod, 24° day, 8° night) and analyzed at intervals leaf pair by leaf pair, there is a steady increase in monoterpenes until the time of floral initiation, followed by a rapid decrease. It is suggested that monoterpenes may serve as substrates for energy metabolism in the secretory cells after other stored substrates have been depleted.     

Effect of Intercalated Long Days and Light Interruption of Dark Period on Flowering, Extension Growth and Senescence of impatiens balsamina

Plants of Impatiens balsamina L. grown under long days were divided into 5 lots to receive 1, 2, 4, 8 and 16 consecutive short day (SD) cycles respectively. Each lot was divided into 5 groups to receive 1, 2, 4, 8 and 16 long day (LD) cycles subsequent to SD regime and the cycles were repeated till the end. Observations on the number, position and time of emergence of floral buds, flowers and extension growth were recorded. The floral buds are initiated and these develop into flowers even when Individual SDs are intercalated with 16 LD cycles, showing that the sub-threshold stimulus is not wiped off but becomes effectively summated through a long non-inductive period. The floral bud initiation in lots receiving less than 4 and flowering in those receiving less than 8 consecutive SD cycles are delayed with decreasing number of consecutive SDs and increasing number of intercalating LDs. This progressive delay is probably due to the delay that is caused by these treatments in the completion of requisite number of SD cycles. The first node to show floral bud initiation is shifted up with increasing intercalated LDs only in plants receiving less than 4 SD cycles and not in those receiving more. Some of the lower floral buds in plants receiving less than 8 consecutive SD cycles either abort or revert to vegetative growth. The first node to flower is, therefore, shifted up. The number of such buds increases either with a decrease in the number of consecutive SDs or an increase in the number of intercalated LDs. The number of floral buds produced in plants receiving 2 or more and flowers in those receiving 4 or more consecutive SD cycles does not differ much with the number of intercalated LDs, but decreases in those receiving less number of SDs. Some nodes bear more than one floral bud and flower. Such nodes are observed in plants receiving individual SD cycles only when intercalated with individual LDs but in all groups in plants receiving 16 consecutive SD cycles. The rate of extension growth increases with an increase in the number of consecutive SDs. The rate in plants receiving individual SDs closely resembles that of plants grown under continuous LDs and that of consecutive 16 SDs with that of control SD plants. The attainment of maximum and the consequent steep fall preceding senescence is successively delayed with an increase in the number of intercalated LDs in plants receiving 16 consecutive SD cycles. Light interruption of the dark period inhibits both the initiation of floral buds and their development Into flowers. showing that in this plant. short days are necessary both for the initiation of floral buds and their development into flowers.     

PHYSIOLOGICAL STUDIES ON THE VERTICILLIUM WILT DISEASE OF TOMATO

The water loss per unit leaf area of tomato plants was decreased after inoculation with Verticillium albo-atrum. When diseased plants began to wilt water loss temporarily increased, but then rapidly decreased to become less than that of healthy plants grown under conditions of adequate or restricted water supply.
The transpiration of excised leaves from plants grown with a restricted water supply was reduced, but not so severely as that of comparable leaves from infected plants. Water loss from leaves on infected plants was reduced irrespective of any blocking of the petiolar xylem.
The rate of water loss from turgid leaf disks on mannitol solutions, and the rate of water uptake of leaf disks on water was similar for disks cut from wilting or turgid leaves of diseased plants or healthy plants grown with an adequate or restricted water supply.
Disease or poor water supply reduced leaf growth but had no effect on the rate of leaf initiation. Although the density of stomata was higher on leaves of diseased plants the stomatal area was less than on healthy plants.
The resistance to water flow in diseased stems was high and was correlated with vessel blockage. About half the blocked vessels contained hyphae. The severity and localization of symptoms in inoculated plants growing on susceptible or resistant rootstocks was directly related to the extent of invasion by the pathogen and to vessel blockage.
Experiments on the wilting activity of cell-free filtrates from cultures of the pathogen in vitro indicated that it produced a stable substance, not an enzyme, that caused wilting in cut shoots by blocking the end of the stem. It is suggested that an increasing internal water shortage causes major symptoms of disease.     

Natural variation in the regulation of leaf senescence and relation to other traits in Arabidopsis

Leaf senescence results in the recycling of nutrients, thereby providing resources required for growth and reproduction. In this study, the effect of day-length on leaf senescence in eight different Arabidopsis thaliana ecotypes was determined and the relationship between senescence and other morphological and life history traits was analysed. A significant variation in the start and extent of leaf senescence depending on the genetic background and the response to day-length was found. Whereas senescence of early flowering ecotypes was accelerated by long days, no effect of day-length on senescence could be found in late flowering Kas-1 plants. Senescence in the different ecotypes was associated with other traits, such as floral transition, the total number of fruits, the total number of leaves and the maximum chlorophyll content. Plants that bolted early also senesced early, produced fewer leaves, accumulated less chlorophyll, but produced more fruits. The present results indicate that senescence may be a key component in the trade-off between investment in photosynthetic capacity and reproduction. The relationship between senescence and other traits was maintained independent of whether differences in senescence were caused by genetic (ecotype) or environmental (day-length) variation, suggesting that genetic and environmental factors affect these traits through common regulatory pathways.     

光周期对菊花花芽分化及其叶片和芽内源多胺含量的影响

以切花菊品种神马为材料,研究不同光周期(16h昼/8h夜;12h昼/12h夜;8h昼/16h夜)对菊花花芽分化过程中叶片和芽内腐胺(Put)、亚精胺(Spd)和精胺(Spm)含量的影响.结果显示:(1)16h/8h处理植株始终没有花芽分化,8h/16h处理的花芽分化开始和完成分别在处理后第13.9天和第23.1天出现,比12h/12h处理的分别提前1.7d和2.8d.(2)16h/8h处理叶片和芽中Put、Spd和Spm含量始终都没有明显变化,而8h/16h和12h/12h处理的叶片和芽中Put、Spd、Spm含量都比16h/8h处理的明显增加,而且8h/16h和12h/12h处理的叶片Put和Spd含量在处理第10天和第20天时出现2个高峰,芽中Put和Spd含量在处理第15天时出现一个高峰;另外,8h/16h处理的叶片和芽中Put、Spd含量比12h/12h处理的有所增加,但差异不显著.结果表明,菊花神马是质型短日照植物,短日照可诱导神马叶片和芽内合成多胺,而且日照时数越短,越有利于叶片和芽内Put、Spd、Spm的积累和促进花芽分化.     

A Comparison of the Disease Reactions of Stems and Detached Leaves of Soil and in vitro Grown Plants and Regenerants of Oilseed Rape to Leptosphaeria maculans and Protocols for Selection for Novel Disease Resistance

Protocols for selecting plant tissues of winter oilseed rape (Brassica napus subsp. oleifera) with resistance to Leptosphaeria maculans by either stem or leaf inoculation of both soil and in vitro grown plant material are described. The stem inoculation procedure gave good correlation (r = 0. 92) between the 50 day stem disease scores of eight out of nine cultivars of soil grown winter oilseed rape inoculated with isolate 41A4 of L. maculans and the N. A. B. esistance ratings or resistance data from field trials. The exception was the cultivar Liradonna. Inoculation of stems of five cultivars with isolates 41A4, 433 and 478 indicated a range of isolate virulence 478 > 41A4 > 433. This was the inverse of that observed in leaf inoculations. Application of the stem inoculation procedure to in vitro shoot cultures allowed differentiation of resistant and susceptible cultivars, including the cultivar Liradonna, after 20 days incubation at 20°C. The protocol was also applicable to plantlets regenerated from thin cell layer explants grown in vitro. Inoculations with isolate 433 allowed the differentiation of resistant, intermediately resistant and susceptible leaf material of soil grown plants, when leaf discs from young leaves were incubated on water agar supplemented with BAP (1 × 10^?5 M) at 25°C for 10 days. Intermediately resistant leaves were resistant after 10 days and susceptible after 15 days of incubation. Leaves of shoot cultures grown in vitro were more susceptible than the corresponding soil grown material. However, inoculation of old leaves with isolate 41A4 (an isolate of less virulence on leaves than 433) distinguished the cultivars after 15 days of incubation. These protocols allow the accurate assessment of resistance to L. maculans at the stem or leaf level and are of use in traditional as well as in vitro selection programmes.     

Studies of the infection of the winged bean by Synchytrium psophocarpi in Papua New Guinea

Infection of leaves and stems of Psophocarpus tetragonolobus by Synchytrium psophocarpi only occurred following spray inoculation of motile zoospore suspensions and incubation for a minimum of 12 h in polyethylene bags or a mist chamber. The incubation period was 7 days and generation time 22 days at temperatures of 31 ^oC max, 24 ^oC min and r.h. of 90% max, 70% min. Young, 1–2 day-old leaves were most susceptible; there was no infection on 10 day-old leaves and susceptibility was not increased by the removal of leaf waxes. No infection occurred when plants were grown from seed from infected pods, seed inoculated with zoospores or sporangia and seed sown in soil containing infected leaf debris. Resting spores were not found in infected tissues stored for 12 wk or in plant debris. S. psophocarpi did not infect Arachis hypogaea, Glycine max, Phaseolus aureus, P. coccineus, P. vulgaris, Pisum sativum, Psophocarpus scandens, Vicia faba, Vigna sesquipedalis and V. unguiculata. S. minutum did not infect winged bean. Inoculation confirmed the susceptibility of the winged bean lines UPS 62, UPS 122, UPS 126 and resistance of two Thai winged bean lines 1602/1 and 1611/2.     

Effect of Sodium Chloride Stress and Nitrogen Source on Respiration, Growth and Photosynthesis in Lucerne (Medicago sativa L.)

The effects of salinity at different light intensities on freshweight growth and on carbon dioxide influx and efflux were examinedin young plants of lucerne (Medicago sativa L.) that had beengrown in solution culture with nitrogen supplied either as nitrateor by a symbiotic rhizobium. Although the inoculated plantsgrew more slowly than those supplied with nitrate, NaCl at alevel equivalent to an osmotic stress of –0.3 MPa didnot reduce the growth rate of either type of plant under a 12h day-length in a growth chamber. With a day-length of 5 h saltstress (0.0 to –0.6 MPa) did not greatly affect grossphotosynthesis of plants grown on nitrate but respiration ratereached a maximum at –0.3 MPa and declined at larger saltconcentrations. Salt diminished both gross and net photosynthesisin the inoculated plants at a 5 h day-length without stimulatingrespiration. The relationship between photosynthesis and respiration as thephoton flux density was successively decreased was used to inferthe effect of salt on maintenance respiration of the plantssupplied with nitrate. Growth and maintenance components ofrespiration could not clearly be separated in the inoculatedplants suggesting that these were unable to maintain themselvesunder the combined stresses of salt and low light intensity.This view was supported by chemical analysis of the plant material.We conclude that the failure of the inoculated plants to adaptto these conditions could be attributed to the greater demandfor assimilates by the rhizobium. Key words: Medicago sativa, Nitrogen source, Salt stress     

Light effects on development of an indeterminate plant

The peanut (Arachis hypogaea L.) plant is indeterminate in growth habit and day-neutral with respect to flower initiation. The Spanish-type cultivar used in this study begins flowering 3 to 4 weeks from planting under optimum environmental conditions. In this study, irradiance and photoperiod were used to alter the development of the peanut plant. Plants grown at low irradiance (300 microeinsteins per square meter per second) had the same number of leaves as the plants grown at high irradiance (500 microeinsteins per square meter per second), but they had a larger leaf surface area and were taller than plants grown at the high irradiance. However, flowering and other reproductive components (pegs, pods, and seeds) were reduced at low irradiance. Comparison of 8-, 12-, and 16-hour photoperiods at the high irradiance showed that the 16-hour photoperiod produced the largest amount of vegetative, but least amount of reproductive components. The plants grown at 8-hour photoperiod had one-third as much total leaflet area as plants grown at 16 hours, but six times more weight of mature seeds. The larger amount of photosynthetic surface (leaf area) did not result in more reproductive growth. The results indicate that the peanut plant may readily redistribute its available assimilates between vegetative and reproductive growth in response to irradiance and photoperiod.     

Effects of Bean Leaf Age on Pathogenicity by Botrytis fabae

Leaves from field bean plants grown out of doors were inoculated with conidia of B. fabae immediately after detaching from stems. The oldest leaves developed more lesions than youngest ones, although they were not chlorotic. On intact plants at high humidities, established lesions on young leaves increased in size at only half the rate of those on old. but still green leaves. Seven days after inoculation a higher proportion of lesions on old leaves bore conidia than those on young leaves, but leaf age had no significant effect on numbers of conidia per mm² of lesion area. Young leaflets from bean plants grown in a controlled environment or in the field challenged with β. cinerea accumulated more phytoalexins than did old ones.