SEASONAL CHANGE IN THE DISTRIBUTION OF CELL SIZE OF COCCONEIS SCUTELLUM VAR. ORNATA (BACILLARIOPHYCEAE) IN RELATION TO GROWTH AND SEXUAL REPRODUCTION1

Growth and sexual reproduction of the marine littoral diatom Cocconeis scutellum Ehrenb. var. ornata Grun. were investigated at 30 different combinations of temperature (5, 10, 14, 18, 22° C), irradiance (20, 60, 100 μE·m^?2·s^?1) and daylength (14:10 and 10:14 h LD cycle). Growth occurred at all combinations. The optimal growth was observed at 14–18° C, long daylength and highest-to-moderate irradiance, and at 18° C, short daylength and highest irradiance. Sexual reproduction on the other hand occurred between 5 and 18° C, and the optimal condition was 10–14° C and short daylength. Annual cyclic, and sesonal changes in the distribution of cell size (valve length) were observed in a field population. These changes were characterized by an annual minimum in mean cell size in autumn, an annual maximum in winter, a slight decrease from the mean in spring–middle summer, a rapid decrease from the mean in late summer–early autumn, and appearance of bimodal distribution of cell size in winter. These changes were caused by sexual reproduction in autumn, rapid growth in late summer–early autumn and slow growth in other seasons, and poor viability of small cells near the lower end of the size range.     

Influence of day length and temperature on number of main stem leaves and time to flowering in lupin

A growth chamber experiment was carried out to investigate the influence of day length and temperature on the development of flowering in eight varieties of the three grain lupin species Lupinus albus (Wat and C3396), L. angustifolius (Gungurru, Polonez and W26) and L. luteus, (Juno, Radames and Teo). The plants were grown at two temperatures, 10°C and 18°C, in combination with five daylength regimes: 10, 14, 18, 24 h day at full light intensity and 10 h full light extended with 8 h low intensity light. Increased daylength decreased days from sowing to flowering in all varieties, but had little effect on thermal time to flowering in most varieties. However, C3396, W26 and Radames had a significantly longer thermal time to flowering at high, non‐vernalising temperature (18°C) at short daylengths. Low light intensity daylength extension did not significantly influence thermal time to flowering. For flower initiation, measured as number of leaves on the main stem three types of response were found. All varieties formed fewer leaves on the main stem at 10°C than at 18°C, although the two thermo‐neutral varieties of L. luteus, Juno and Teo, gave only a small response to temperature and daylength. In Polonez, Gungurru and Wat, low temperature decreased leaf number, but there was only a small response to changes in daylength. Three varieties, C3396, W26 and Radames, showed longer thermal time to flowering at 18°C with short daylengths. This could be explained by a greater number of main stem leaves formed at short daylength at non‐vernalising temperatures. Increased daylength decreased leaf number in these varieties, but never to a smaller number than for plants grown at 10°C. In these varieties, low intensity extension of the daylength had a similar (W26, Radames) or decreased (C3396) effect compared to full light extension. The hastening of time to flowering by long days could be separated into two effects: a high light energy effect hastened development by increasing the rate of leaf appearance in all varieties, while low light energy in thermo‐sensitive varieties was able to substitute for vernalisation by decreasing leaf number.     

Induction and termination of diapause inOrius predatory bugs

Photoperiodic induction of reproductive diapause at 18°C was investigated in fourOrius [Heteroptera: Anthocoridae] species.Orius insidiosus (Say) displayed a long-day response with a critical photoperiod between L11:D13 and L12:D12. Diapause in this species was terminated rapidly when the temperature and/or the daylength were increased.Orius majusculus (Reuter) also displayed a long-day response. The critical photoperiod fell between L14:D10 and L16:D8. Diapause in this species was not terminated within 14 days when both temperature and daylength were increased. InOrius albidipennis (Reuter) no diapause could be induced at photoperiods varying from L8:D16 to L16:D8. InOrius tristicolor (White) a high proportion of diapause was found at all photoperiods tested. The effect of temperature on photoperiodic induction of diapause was studied inO. insidiosus at L10:D14. Diapause occurred at 18°C, 21°C and 25°C, but not at 30°C. Again, diapause was terminated rapidly after transfer to 25°C/L16:D8. Exposing only the nymphal instars 1–5 to short daylength was not enough to induce diapause in the whole population ofO. majusculus. Orius predatory bugs are used as biocontrol agents against western flower thrips,Frankliniella occidentalis (Pergande) [Thysanoptera: Thripidael, in greenhouses. The consequences of photoperiodic induction of diapause for the success of early season releases ofOrius are discussed.     

Photoperiodic control of larval development in the semivoltine cockroachPeriplaneta japonica (Blattidae: Dictyoptera)

Periplaneta japonica is semivoltine, entering early diapause in any (except the first) larval instar before the last, and late diapause in the last instar. Early diapause was induced under a short day of 13 h or less at 28°C, and under both short and long daylength (12–16 h) at 20°C. The shorter the daylength and the lower the temperature, the younger the instar was entering early diapause. Early diapause was terminated by a long day (16 h) or a high temperature (28°C), after which larvae grew faster in short days than in long days until the last instar, when they again entered diapause, always in short days and frequently in long days. This late diapause was terminated also by an increase in daylength and was always followed by adult emergence. In this case, 13 and 14 h daylengths after exposure to 12 h daylength were as effective as 16 h daylength. Ourdoor samples collected in late autumn, winter and early spring at Hirosaki (40.5°N) comprised two distinct size groups, corresponding with the early and late diapause instars. Based on these results, the seasonal development strategy and intriguing aspects of the photoperiodic response in this cockroach are discussed.     

TEMPERATURE,PHOTOPERIOD AND LIGHT INTERACTIONS ON GROWTH AND FERTILITY OF GLOSSOPHORA KUNTHII (PHAEOPHYTA,DICTYOTALES) FROM CENTRAL CHILE1

Excised ligulae of Glossophora kunthii from central Chile were cultured of temperatures of 5–25° C, photoperiods of 16:8 and 8:16 h LD cycles, with photon irradiances of 10 and 50 μmol · m^?2· s^?1. Growth of the ligulae, number of fertile ligulae and number of tetrasporangia forming on the ligulae were assessed. Ligulae tolerated temperatures between 10 and 23°C. Temperature interacted with daylength and photon dose, determining quantitative responses in the growth and fertility of ligulae. Growth was least at 8:16 h LD and was not affected significantly by temperature. It was greatest at 16:8 h LD, 50 μmol · m^?2· s^?1 and increased with temperature up to 20°C. Percentage of fertile ligulae and number of tetrasporangia increased with temperature at the 8:16 h LD cycle, reaching a maximum at 20°C. Fertility was low at 16:8 h LD, except at 20° C (and low photon dose) suggesting that reproduction at 20° C is independent of daylength in this species. Ligulae grew larger at the long-day photoperiods and the proportions of fertile ligulae were higher at the short-day photoperiods, irrespective of the total photon dose received. These results suggest that some aspects of growth and fertility are controlled by photoperiod.     

Flowering of Stylosanthes guianensis in Relation to Juvenility and the Long-Short Day Requirement

Seedlings of Stylosanthes guianensis var. guianensis were grownin long (14 h) days in five temperature regimes for varyingperiods before transfer to short (11 h) days at 30 ?C/21 ?C.The juvenile phase before seedlings responded to inductive conditionswas c. 45–50 d, 50–60 d and 60–70 d for cv.Schofield, cv. Cook and C.P.I. 34906 respectively, which ispositively related to their critical photoperiod for flowering.Temperatures favourable for growth (e.g. 30 ?C/26 ?C) reducedthe juvenile phase in C.P.I. 34906 and in Cook, which did notflower in 11 h days unless previously exposed to more than 18long days. In a second experiment cv. Cook was confirmed as a long-shortday plant. Seedlings were grown for 50 d in a glasshouse withnatural daylength extended to 13, 14, 16 or 24 h before transferto 12 h photoperiods. Cook floral development was positivelyrelated to daylength provenance before transfer and plants incontinuous 12 h did not flower. Shortening daylength after 48 cycles of 12 h to 11.75 h didnot result in continued floral development in Cook plants butcv. Graham plants were initiated or transitional by 75 d. Key words: Stylosanthes guianensis, Photoperiod, Temperature, Flowering     

Photoperiod and temperature as triggers in the seasonality ofDelesseria sanguinea

The red algaDelesseria sanguinea is strongly seasonal, producing gametangia in early tetrasporangia in mid- and new blades in late winter. A lamp was installed in the shallow subtidal off the Isle of Man, illuminating about 40 plants ofDelesseria for one hour in the night or day. Single blades from separate plants were held in laboratory tanks at different temperatures and in short days, long days and with a night-break. In the sea, the night-break prevented fertility in tetrasporophytes but some gametophytes became fertile. New blades were stimulated, arising 6 weeks early. Their lengths indicated a saturation level of about 10 μmol m⁻² s⁻¹ for one hour in 24. Growth rate calculations suggested a delay in stimulation until the ambient sea temperature dropped to 13°C. Tetrasporangia were formed after the night-break ceased in December but not January. In day-addition of light there was slight, if any, stimulation of blade production. In the laboratory, gametogenesis occurred readily in short days but not in long days or with a night-break. There was little or no effect of temperature between 8 and 14°C. Tetraspores were rarely formed in the laboratory. The timing of gametogenesis suggested a critical daylength of about 14 h. New blades were clearly stimulated by lower temperatures in the laboratory, few forming at 14°C and many at 7–10°C. They appeared mainly in long days or with a night-break but formed in short days after gametangia production. It is concluded that both gamete and tetraspore production are under photoperiodic control but require different conditions, possibly gametogenesis needing fewer cycles. There is some evidence for antagonism between new blade and reproductive structure initiation. The critical daylength could involve a timing differential of a month over the species geographical range. On the other hand it is suggested that its southern limit could be determined by the winter isotherm of 13°C, warmer than which might not allow blade initiation.     

Photoperiodic induction of larval diapause and temperature-dependent termination in a wild multivoltine bruchid,Kytorhinus sharpianus

A wild bean weevil,Kytorhinus sharpianus Bridwell (Coleoptera: Bruchidae), has a multivoltine life cycle and enters a hibernal larval diapause at the fourth instar under a short daylength (Shimada & Ishihara, 1991). Here, we investigated their diapause incidence under different photoperiods at 24°C and 27°C. The critical photoperiods for diapause induction were 14.5 h at 24°C and 14 h at 27°C. The stages susceptible to diapause-inducing stimuli were estimated by transferring larvae of various instars from long days to short days and vice versa. Then we investigated the incidence of larval diapause. The sensitive stage was estimated to be from the third to early fourth instar. Though larval diapause, which was induced under a short daylength, was terminated only by increasing the daylength, the termination was more synchronized by an exposure to a low temperature followed by increasing temperature, irrespective of photoperiod.     

Photoperiodic response and heritability of the pre-flowering interval of two red clover (Trifolium pratense) populations

The reaction to 12, 14, and 16 h photoperiods of two medium-maturing red clover (Trifolium pratense) populations (cv. Kenland and Cycle 6 of a selection for long stems) under controlled environment conditions was studied. Under both 14 and 16 h photoperiods, Kenland flowered sooner and had shorter stems, more stems per plant, and greater herbage yield per plant but had a similar number of internodes compared to the long stem Cycle 6 population. A daylength between 12 and 14 h was critical for flower initiation in both populations. The critical daylength to induce stem initiation was shorter than the daylength to induce flowering in some genotypes. From half-sib analyses, the narrow–sense heritability of the pre-flowering interval in Kenland ranged from 15 to 23%. The expected response to one cycle of selection (5% selection intensity) for lengthening or shortening the pre-flower interval was 2.3 to 2.4 days at the 16 h photoperiod and 3.0 days at the 14 h photoperiod. Low correlation between pre-flowering interval, stem length, and stem number indicated that it may be possible to change one character without affecting the other two. The need for further studies of the genetic nature of the control of flowering in red clover was indicated.     

Studies on the Photoperiodic Responses in Short-Day Plant Helianthus tubevotus

Plants of Helianthus tuberosus, variety white tuber, were treated with various daylengths of 4, 6, 8, 10, 11, 12, 13, 14, 15, 18 h. for 25 days as soon as six leaves on a plant appeard Irradiation for 6–13 h per day induced the plants to form flower buds and flowering, daylength with 14 h or longer kept the plants in vegetative growth. The experiments showed that this variety of Helianthus tuberosus required short days for flowering and the critical daylength was about 13 h. The plants were treated with short days for different durations. At least 17 days were required, Formation of flower buds and flowering had positive correlation with the number of short days over 17 days. After short-day induction, the shorter the daylength is, the more the flower buds inverted. Long-day treatment after an appropriate period of short days wouid reduce the number of flower and induce new vegetative branches from flowering granehes.     

Floral Initiation of White Clover (Trifolium repens L.) in Response to Daylength and Temperature

The response to different combinations of daylength (14, 15and 16 h) and day/night temperature (20/10°C, 30/15°C)of four white clover (Trifolium repens) varieties in terms offloral initiation and development was studied. More plants flowered under long days (16 h) at 30°C thanin any other combination. Varietal differences in response todaylength were large but temperature was the factor controllinginitiation. Daylength was more important in regulating peduncle length,floret and ovule numbers than was temperature. The amount ofnectar produced was lowest at the higher temperature althoughnectar concentration was unaffected by temperature. Nectar concentrationwas lowest in the shortest daylength (14 h). White clover, floral initiation, temperature, daylength     

Effect of daylength and temperature on the larval diapause of the sunflower moth, Homoeosoma electellum

The effect of daylength and temperature on the regulation of the larval diapause of a central Missouri population of the sunflower moth, Homoeosoma electellum, was examined. Fully grown fourth-instar larvae exhibit a facultative diapause. Measurements of the effect of photoperiod on diapause induction revealed critical photoperiods of about 13 h 30 min light/day at 20°C, and between 11 h 45 min and 12 h light/day at 23°C. Third and fourth-instar larvae were shown to be the main sensitive stages for diapause determination. Daylength was also shown to be an important regulator of the rate of diapause development. A short day of LD 10:14 h permitted only a low rate of diapause development, whereas long days of LD 14:10 h and LD 16:8 h accelerated diapause development at 25 and 30°C. When long days were alternated with short days at 30°C the accelerating effect of long days on diapause development was not found. Systematic transfers of chilled diapausing larvae revealed an accelerated diapause development in groups transferred from 10 to 30°C LD 10:14 h, but diapause development was not accelerated in groups transferred from 10 to 30°C LD 16:8 h.     

A CIRCADIAN RHYTHM IN THE LONG-DAY PHOTOPERIODIC INDUCTION OF ERECT AXIS DEVELOPMENT IN THE MARINE RED ALGA NEMALION HELMINTHOIDES1,2

Two isolates of Nemalion helminthoides from the west coast of Ireland showed a heteromorphic life history in which tetraspores formed under short-day conditions on uniaxial, prostrate tetrasporophytes gave rise to uniaxial, prostrate growths similar in morphology to the tetrasporophytes. The induction of multiaxial, erect axes on tetraspore-derived plants was a long-day photoperiodic response. At 11°C, 16:8 h LD, nitrate concentration in the enriched seawater medium had little effect on the numbers of erect exes formed. Induction of erect axes occurred only in daylengths ≥ 12 h, mainly between 7–13° C, and the critical daylength, which generally lies between 14 and 16 h, changed with temperature. Night-breaks (NB) of 1 h light in the middle of 16 h night were ineffective in the promotion of erect axis formation, and day-breaks (DB) of 1 h darkness in the middle of a 16 h day did not inhibit axis formation. Neither continuous light nor NB of 1–1.5 h given at various times during the dark period of an 8:16 h LD cycle promoted the formation of erect axes. At 9° C, equivalent photon exposures (0.69 and 0.34 mol·m^?2) at two different instantaneous photon flux densities resulted in erect axis formation only in the 14 h, 16 h and DB regimes. Photoregimes of 16 h light in combination with dark cycles of various lengths resulted in the maximal promotion of the formation of erect axes in diurnal (22–24 h) and bi-diurnal (44–48 h) cycles, a diminishing response in non-diurnal cycles greater than 24 and 48 h, and a minimal response at 32 h. These data show that the formation of erect axes is a long-day photoperiodic response and provide further evidence for a connection between endogenous circadian rhythms and long-day photoperiodic responses.     

Photoperiodic and temperature effects on the intensity of larval diapause in Sesamia nonagrioides

Abstract. The intensity of larval diapause in Sesamia nonagrioides Lef (Lepidoptera: Noctuidae) was investigated under laboratory conditions. Newly hatched larvae were exposed to different stationary photoperiods (from LD 7 : 17 h to LD 14 : 10 h), at a constant temperature of 25 °C. Diapause incidence was higher when larvae were exposed to daylengths shorter than the critical value (LD 12 : 12 h), whereas the within‐treatment variation in the larval period appeared to be significantly correlated with the photoperiod applied. The incidences of diapause and the duration of larval development were also measured after exposing larvae to short photoperiods (LD 8 : 16 h, LD 10 : 14 h or LD 12 : 12 h) in combination with various temperatures (20, 22.5 or 25 °C). Although an increase in the incidence of diapause appeared with the lowering of the temperature, no statistical differences were observed in the time needed for pupation within the photoperiodic treatments at the temperatures of 20 and 22.5 °C. Furthermore, when diapausing larvae were transferred to the long photoperiod of LD 16 : 8 h, they immediately proceeded to pupation, regardless of the photoperiod or the temperature to which they had been previously exposed, indicating that there were no differences in the intensity of diapause. Photoperiodic changes from LD 10 : 14 h to LD 12 : 12 h or to LD 14 : 10 h at different larval ages reduced the intensity of diapause with (a) early age of transfer and (b) increase of daylength. By contrast, when larvae were transferred from the long photoperiod of LD 14 : 10 h to shorter, such as LD 10 : 14 h or LD 12 : 12 h, a small increase in the intensity of diapause with the shortening of the daylength was apparent. These results support the hypothesis that insects may compare the duration of the photoperiod and could classify them as either longer or shorter in relation to the critical value.     

Persistence of enterohaemorrhagic and nonpathogenic E. coli on spinach leaves and in rhizosphere soil*

Aims: Survival of Escherichia coli O157:H7 and nonpathogenic E. coli on spinach leaves and in organic soil while growing spinach in a growth chamber was investigated. Methods and Results: Spinach plants were maintained in the growth chamber at 20°C (14 h) and 18°C (10 h) settings at 60% relative humidity. Five separate inocula, each containing one strain of E. coli O157:H7 and one nonpathogenic E. coli isolate were applied to individual 4‐week‐old spinach plants (cultivar ‘Whale’) grown in sandy soil. Leaf and soil inocula consisted of 100 μl, in 5 μl droplets, on the upper side of leaves resulting in 6·5 log CFU plant^?1 and 1 ml in soil, resulting in 6·5 log CFU 200 g^?1 soil per plant. Four replicates of each plant shoot and soil sample per inoculum were analysed on day 1 and every 7 days for 28 days for E. coli O157:H7 and nonpathogenic E. coli (by MPN) and for heterotrophic plate counts (HPC). Escherichia coli O157:H7 was not detected on plant shoots after 7 days but did survive in soil for up to 28 days. Nonpathogenic E. coli survived up to 14 days on shoots and was detected at low concentrations for up to 28 days. In contrast, there were no significant differences in HPC from days 0 to 28 on plants, except one treatment on day 7. Conclusions: Escherichia coli O157:H7 persisted in soil for at least 28 days. Escherichia coli O157:H7 on spinach leaves survived for less than 14 days when co‐inoculated with nonpathogenic E. coli. There was no correlation between HPC and E. coli O157:H7 or nonpathogenic E. coli. Significance and Impact of the Study: The persistence of nonpathogenic E. coli isolates makes them possible candidates as surrogates for E. coli O157:H7 on spinach leaves in field trials.     

ECOTYPIC VARIATION IN CYSTOCLONIUM PURPUREUM (RHODOPHYTA) SYNCHRONIZES LIFE HISTORY EVENTS IN DIFFERENT REGIONS1

Temperature and daylength responses were determined in culture for isolates of the red alga Cystoclonium purpureum (Hudson) Batters from Nova Scotia (NS, Canada), Helgoland (HE, Germany), and Roscoff (RO, France). Most isolates survived temperatures of –1.5°/–2° to 23°C, whereas 25°C was lethal. Only the RO-gametophytes died at 23°C. Optimal growth conditions were 10°–20°C in both long and short days for the NS isolates and 8°–15°C and 8°–18°C at daylengths of >12 h for the RO and HE isolates, respectively. Tetrasporophytes and gametophytes of the NS isolate reproduced at 10°–20°C in long and short days within 5 months. At lower temperatures reproduction was limited or slow. The European isolates formed tetrasporangia at 10°–20°C (HE) or 5°–l8°C(RO), spermatangia at 5°–15°C (HE) or 5°–20°C (RO), and carpospores at 5°–15°C(HE) or 10°–15°C (RO). Short days either blocked or delayed reproduction of the European isolates. The phenology of C. purpureum was studied at Helgoland and Roscoff, where similar seasonal patterns were observed. In early spring, growth was rapid and plants started to form reproductive structures. In summer, tetra-and carpospores were shed followed by degeneration of the upright axes while branched holdfasts persisted. New upright axes and juvenile plants were formed in autumn, but these remained small during the winter months. Published data indicate that the seasonal pattern at Nova Scotia is similar, although the onset of growth and reproduction is delayed until the end of spring. These observations correspond well with the results of the experiments. The life history of C. purpureum is regulated by temperature and daylength. In the eastern Atlantic, the limiting effect of short days confines growth and reproduction to spring and summer. In the western Atlantic, low winter temperatures alone bring about the same seasonal pattern. After plants have reproduced, uprights degenerate in spite of continuing favorable conditions.     

Effects of photoperiod and low temperature on diapause termination in the yellow-spotted longicorn beetle (Psacothea hilaris)

Abstract. .The effects of photoperiod and low temperature on diapause termination in the yellow-spotted longicorn beetle, Psacothea hilaris (Pascoe) (Coleoptera: Cerambycidae), were examined using a population from Ino, Japan. Diapausing insects obtained by rearing larvae under short daylength (12 or 13 h) at 25^oC were subjected to various treatments. When the photoperiod was changed at the same temperature, diapausing larvae showed a long-day response with a critical daylength between 13.5 and 14h. The diapause was terminated and consequently pupation occurred if the daylength was longer than 13.5 h. Chilling the diapausing larvae at 10^oC for 30 or more days also terminated diapause in most larvae irrespective of the photoperiods during and after chilling treatment. In contrast, the post-chilling photoperiod had a critical effect on development of diapausing larvae chilled for only 15 days.     

Flowering of contrasting white clover varieties in relation to daylength in controlled environments and in the field

The effect of 12 , 14 and 16 h photoperiods, given consecutively, on flower production in 10 varieties of white clover (Trifolium repens) in controlled environments, is described. The effect of natural daylengths from September to July on the same plants in the field was also studied in the following year. Relationships between morphological and physiological traits and flowering were examined. In controlled environments most plants flowered under the longest days, three times as many in the 16 h daylength as in the 12 h. Larger leaved types had a higher proportion of reproductive plants than did smaller leaved types. Floral initiation was not observed in the field until daylengths were in excess of 15 h. Increasing daylength increased flower production, floret and ovule numbers but did not appear to increase nectar production significantly.     

Diapause Induction and Termination in the Small Brown Planthopper,Laodelphax striatellus (Hemiptera: Delphacidae)

The small brown planthopper, Laodelphax striatellus (Fallén) enters the photoperiodic induction of diapause as 3rd or 4th instar nymphs. The photoperiodic response curves in this planthopper showed a typical long-day response type with a critical daylength of approximately 11 h at 25°C, 12 h at 22 and 20°C and 12.5 h at 18°C, and diapause induction was almost abrogated at 28°C. The third stage was the most sensitive stage to photoperiod. The photoperiodic response curve at 20°C showed a gradual decline in diapause incidence in ultra-long nights, and continuous darkness resulted in 100% development. The required number of days for a 50% response was distinctly different between the short- and long-night cycles, showing that the effect of one short night was equivalent to the effect of three long nights at 18°C. The rearing day length of 12 h evoked a weaker intensity of diapause than did 10 and 11 h. The duration of diapause was significantly longer under the short daylength of 11 h than it was under the long daylength of 15 h. The optimal temperature for diapause termination was 26 and 28°C. Chilling at 5°C for different times did not shorten the duration of diapause but significantly lengthened it when chilling period was included. In autumn, 50% of the nymphs that hatched from late September to mid-October entered diapause in response to temperatures below 20°C. The critical daylength in the field was between 12 h 10 min and 12 h 32 min (including twilight), which was nearly identical to the critical daylength of 12.5 h at 18°C. In spring, overwintering nymphs began to emerge in early March-late March when the mean daily temperature rose to 10°C or higher.     

Photoperiodic Regulation of Photosynthate Partitioning in Leaves of Digitaria decumbens Stent

In leaves of pangolagrass (Digitaria decumbens Stent.), the proportion of photosynthate partitioned into starch adjusts to a change in daylength within 24 hours. After a single 14-hour long day, the relative starch accumulation rate is approximately 50% of that under 7-hour short days. This rapid response was exploited to study the light requirement for the perception of changes in daylength. It was found for short day-grown plants that: (a) 7-hour daylength extensions with dim white light (below the light compensation point for photosynthesis); (b) 7-hour daylength extensions with dim far red light (wavelengths greater than 690 nanomoles); or (c) 0.5-hour night-break irradiations with bright white light were all capable of producing about one-half of the effect of a 7-hour daylength extension with bright light. However, long periods of bright light were not required for a complete effect, since a 7-hour shifted short day (i.e. beginning 7 hours later than usual) was as effective as a 14-hour-long day itself. There was also a critical daylength between 11 and 12 hours for the transition between short-day and long-day partitioning patterns. Photoperiod determination depends, at least in part, on a nonphotosynthetic photoreceptor sensitive to both visible and far red irradiation. The duration of the photosynthetic period, as shown in experiments with low-pressure sodium lamps, does not by itself determine the response to daylength.