The effect of temperature on the photoperiodic 'counters' for female morph and sex determination in two clones of the black bean aphid, Aphis fabae

Experiments were performed on two clones of the black bean aphid, Aphis fabae Scopoli – one from Aberdeen, Scotland (57°N), the other from Cambridge, England (52°N) ? to determine the number of long- or short-night cycles required for 50% induction of winged versus wingless females on the one hand and males versus females on the other (i.e. required day number, RDN), at three temperatures, 12.5, 15 and 17.5°C. In the case of female morph determination, the RDN for long-night cycles was temperature compensated, whereas that for short-night cycles was highly temperature dependent. For sex determination, the RDN for long-night cycles was again temperature compensated, whereas, due to the mechanism of sex determination, male production was close to 100% in our protocol, even with a maximal number of short-night cycles, and the RDN could therefore not be assessed. Model-generated response curves, using the recently developed ‘double circadian oscillator model’ for photoperiodic time measurement in insects and mites, closely resembled the observations. It could also be shown that differences observed between response curves of female morph and sex determination in the Scottish clone were due, according to the model, to differences in their photoperiodic ‘counters’, rather than to differences in their clocks.     

Photoperiodic counter of diapause induction in Pseudopidorus fasciata (Lepidoptera: Zygaenidae)

Induction of larval diapause is a photoperiodically controlled event in the life history of the moth Pseudopidorus fasciata. In the present study, the photoperiodic counter of diapause induction has been systematically investigated. The required day number (RDN) for a 50% response was determined by transferring from a short night (LD 16:8) to a long night (LD 12:12) or vice versa at different times after hatching, The RND differed significantly between short- and long-night cycles at different temperatures. The RDN for long-night cycles at 20, 22, 25 and 28 degrees C was 11.5, 9.5, 7.5 and 8.5 days, respectively. The RDN for short-night cycles was 3 days at 22 degrees C and 5 days at 20 degrees C indicating that the effect of one short night was equivalent to the effect of 2-3 long nights effect. Night-interruption experiments of 24h photoperiods by a 1 h light pulse showed that the most crucial event for the photoperiodic time measurement in this moth was whether the length of pre-interruption (D(1)) or the post-interruption (D(2)) scotophases exceeded the critical night length (10.5 h). If D(1) or D(2) exceeded 10.5 h diapause was induced. The diapause-averting effect of a single short-night cycle (LD 16:8) against a background of long nights (LD 12:12) showed that the photoperiodic sensitivity was greatest during the first 7 days of the larval period and the highest sensitivity was on the fourth day. Both non-24 and 24 h light-dark cycle experiments revealed that the photoperiodic counter in P. fasciata is able to accumulate both long and short nights during the photosensitive period, but in different ways. The information from short-night cycles seems to be accumulated one by one in contrast to long-night cycles where six successive cycles were necessary for about 50% diapause induction and eight cycles for about 90% diapause. These results suggest the accumulation of long-night and short-night cycles may be based on different mechanisms.     

Embryogenesis and oögenesis in alate virginoparae,gynoparae, and oviparae of the aphid Myzus persicae, in relation to photoperiod

The study reports on the effects of prenatal and/or postnatal exposures to short-night or long-night conditions, and of crowding, on embryogenesis and oögenesis in alate virginoparae, gynoparae, and oviparae of a holocyclic strain of the green peach aphid, Myzus persicae, from Yakima, Washington State.In alate virginoparae raised at a density of 10–20 per radish seedling in a short-night regime (8 hr darkness per diem), 3–4 embryos occurred in each of their 10 ovarioles, when the aphids attained adulthood. More than 30 larvae were deposited by most of these alatae. However, in young adult gynoparae, raised at these densities in a long-night regime (15 hr darkness per diem), only one viable embryo (a presumptive ovipara) occurred per ovariole. The follicle containing this embryo was followed by 1–2 abnormal follicles in each ovariole, and the number of larvae deposited by a gynopara was generally less than 10. In young adult oviparae similarly raised under a long-night regime, only one egg typically occurred in each of their 10 ovarioles, and the eggs deposited by an ovipara (only after it had mated) generally numbered less than 10. Alate virginoparae and gynoparae contained an additional embryo in some of their ovarioles when these morphs were raised at a lower density (1–5 per plant).Presumptive gynoparae partially developed the reproductive features of alate virginoparae when transferred to a short-night regime at birth; the converse was true when presumptive alate virginoparae were transferred to a long-night regime early in larval life. Oviparae maintained in short nights from before birth developed the appearance of apterous virginoparae but still produced eggs rather than embryos. However, their oögenesis was enhanced and eggs (10–20) were deposited by them without prior mating. Under all regimes tested, oviparae were always deposited early in the larviposition sequence of their alate mothers, and the number of oviparae deposited never exceeded 15.The possible involvement of juvenile hormone in the regulation of these events and the ecological significance of the results are discussed.     

Differential photoperiodic responses in genetically identical winged and wingless pea aphids, Acyrthosiphon pisum, and the effect of day length on wing development

Abstract. Winged and wingless individuals of a pink clone of the pea aphid, Acyrthosiphon pisum (Harris), showed differences in the response curves for photoperiodic induction of both males and sexual females (oviparae). The critical night length (CNL) for ovipara induction in winged aphids was 0.75 h shorter than in wingless aphids, whereas the CNL for male induction in winged aphids was 1.0h longer than in wingless aphids. This means that in winged aphids the CNL for male induction in winged aphids was 0.5 h longer than that for ovipara induction, while in wingless aphids the CNL for male induction was 1.0–1.5 h shorter than that for ovipara induction, and also the shapes of the curves differed.
Winged aphids were produced by wingless mothers which were crowded as young adults. However, when young adults were crowded in long nights, winged aphids were not produced, and the CNL for wing inhibition was between 9.5 and 10h. This effect of photoperiod on wing induction was maternal.     

Response to photoperiod during diapause development in the spider mite Tetranychus urticae

To study the question whether photoperiodic time measurement in the spider mite Tetranychus urticae is based on a qualitative or quantitative principle, the duration of diapause development was determined in individual females at various constant photoperiods at 19 degrees C. Diapause duration at all four long-night treatments fluctuated around 64.5 days, varying from 62.2 at LD 12:12h to 66.4 at LD 10:14h. The within-treatment variation in diapause duration of the long-night groups appeared to be significantly correlated to the nightlength of the photoperiods used; the longer the nightlength, the higher the within-treatment variation. Frequency distributions of females completing diapause under the two regimes with nightlengths near the critical nightlength were skewed to the right. Mean diapause durations at these regimes, LD 13:11h and LD 14:10h, were 25.4 and 11.9 days, respectively. Mites completed diapause rapidly and synchronously under the three short-night photoperiods tested; within two weeks after transfer from cold storage at 4 degrees C to the diapause terminating regimes at 19 degrees C all females started reproduction. Mean diapause durations were 8.1, 6.4 and 6.5 days for the short-night treatments LD 15:9h, LD 17:7h and LD 19:5h, respectively. The coefficients of variation of diapause duration (variability within groups relative to the mean) of the short-night and the long-night groups varied from 18 to 42%; the coefficients of the two intermediate groups were 69and 81%. There was a clear difference in diapause duration between long-night and short-night groups, but no significant difference was present in this characteristic between different long-night groups on the one hand and only a small difference between different short-night groups on the other. These results support the hypothesis that photoperiodic time measurement in the spider mite is based on a qualitative principle; photoperiods are classified as either 'long' or 'short' in relation to a 'critical' photoperiod. However, around the critical nightlength, intermediate responses were observed which might hint at the quantitative nature of the underlying mechanism. Therefore, although most results are in agreement with the hypothesis of a qualitative mechanism, it cannot be excluded that photoperiodic time measurement in the spider mite is based on a quantitative principle.     

The photoperiodic responses and phenology of an English strain of the pea aphid Acyrthosiphon pisum

Abstract. 1. The response curves for the photoperiodic induction of the sexual forms (oviparae and males) differ significantly in an English clone of the pea aphid Acyrthosiphon pisum Harris. Male production is sharply peaked. The late summer scotophases (dark periods) that initiate male production are 1.0–1.5 h shorter than those that initiate ovipara production; the induction of males, but not oviparae, virtually ceases at scotophases longer than 12 h. This disparity suggests that there are two photoperiodic clocks.
2. All ovipara-producing aphids switch spontaneously to virginopara production part-way through the progeny sequence, irrespective of photoperiod. This may confer the ability to overwinter partheno-genetically under favourable climatic conditions. Since males are always born last in the progeny sequence this possibility would be pre-empted unless the terminal male sequences were suppressed by long winter scotophases.
3. The role of the photoperiodic response in determining the seasonal phenology was tested in the field by exposing a succession of laboratory-reared aphids to natural photoperiods, in late summer and autumn. Adult males and oviparae developed synchronously in early October, the difference in critical scotophase compensating for the late appearance of males in the progeny sequence. A large part of the 'civil twilight' is photoperiodically active.
4. Clones propagated outdoors by isolating aphids in each generation from the terminal sequence of virginoparae did not survive the whole winter of 1985/86. The chances of survival were reduced by severe weather and by the inability of the photoperiodic system to 'turn off' the production of early born oviparae which are, therefore, 'wasted'.     

A comparison of photoperiodic control of diapause between aestivation and hibernation in the cabbage butterfly Pieris melete

In the cabbage butterfly, Pieris melete, summer and winter diapause are induced principally by long and short daylengths, respectively; the intermediate daylengths (12-13 h) permit pupae to develop without diapause. In this study, photoperiodic control of summer and winter diapause was systematically investigated in this butterfly by examining the photoperiodic response, the number of days required to induce 50% summer and winter diapause and the duration of diapausing pupae induced under different photoperiods. Photoperiodic response curves at 18 and 20 degrees C showed that all pupae entered winter diapause at short daylengths (8-11 h), the incidence of diapause dropped to 82.3-85.5% at 22 degrees C without showing a significant difference between short daylengths, whereas the incidence of summer diapause induced by different long daylengths (14-18 h) was varied and was obviously affected by temperature. By transferring from various short daylengths (LD 8:16, LD 9:15, LD 10:14 and LD 11:13) to an intermediate daylength (LD 12.5:11.5) at different times after hatching, the number of cycles required to induce 50% winter diapause (7.28 at LD 8:16, 7.16 at LD 9:15, 7.60 at LD 10:14 and 6.94 at LD 11:13) showed no significant difference, whereas by transferring from various long daylengths (LD 14:10, LD 15:9, LD 16:8 and LD 17:7) to an intermediate daylength (LD 12.5:11.5) at different times, the number of cycles required to induce 50% summer diapause (5.95 at LD 14:10, 8.02 at LD 15:9, 6.80 at LD 16:8, 7.64 at LD 17:7) were significantly different. The intensity of winter diapause induced under different short daylengths (LD 8:16, LD 9:15, LD 10:14 and LD 11:13) was not significantly different with an average diapause duration of 87 days at a constant temperature of 20 degrees C and 92 days at a mean daily temperature of 19.0 degrees C, whereas the intensity of summer diapause induced under different long daylengths (LD 14:10, LD 15:9, LD 16:8 and LD 17:7) was significantly different (the diapause duration ranged from 75 to 86 days at a constant temperature of 20 degrees C and from 76 to 88 days at a mean daily temperature of 19.0 degrees C). All results suggested that photoperiodic control of diapause induction and termination is significantly different between aestivation and hibernation.     

Photoperiodic determination of the male and female sexual morphs of Myzus persicae

The chronology of the photoperiodic determination of sexual morphs in holocyclic Myzus persicae was studied in the laboratory by transfer of synchronized batches of aphids between long-day (16 hr) and short-day (10 hr) régimes at a constant temperature of 20°C. The length of exposure to the short-day régime was measured in terms of the number of long dark-periods received by the aphids. The photoperiodic response extended over four generations (P, G₁, G₂, and G₃ respectively). When P generation aphids were given short days from the fourth instar, alate viviparae and males appeared successively in generation G₂, oviparae in G₃. Increasing the number of long dark-periods received during the development of G₂ embryos had a cumulative effect on the number which developed into alate viviparae. Determination of all the first-born G₂ aphids as alatae occurred only if their mothers had been exposed to the short-day régime throughout larval development. Alate viviparae gave birth to oviparae if they received a minimum of 4 long dark-periods, starting from a late stage in their embryonic development. The critical stage for ovipara determination in the G₃ embryo was on the sixth or seventh day after ovulation, more than half-way through embryonic development. G₂ aphids were determined as males before ovulation if their parents received 4 (in some circumstances only 3) long dark-periods. In the clones studied, male determination, once initiated in the G₁ parent, could not be reversed by later back-transfer to the long-day régime.     

Laboratory-simulated naturally-decreasing day lengths, twilight and aphid photoperiodism

Abstract. Day-length changes, as well as periods of twilight, that occur in the course of each natural day-night cycle, were recreated for two chosen latitudes in a computer-controlled 'natural-day-length simulator'.The photoperiodic responses of two aphid species, Aphis fabae and Megoura viciae , were examined in conditions which mimicked late summer to autumn at two simulated latidudes, 51.5N (e.g.Ascot, Southern Britain) and 60°N (e.g.southern tip of Shetland Islands, Northern Britain), with temperatures between 16°C ('night') and 18°C ('day').The responses under simulated natural photoperiodic conditions were similar to those observed under conventional experimental conditions of squarewave light-dark cycles (with abrupt lights-on and lights-off and constant light intensities during the light phase): both aphid species responded to civil twilight as light, and the critical day lengths (including civil twilight) for the induction of sexual morphs by the two aphid species observed in the simulator were the same as those found in squarewave light-dark cycles.
Autumn field experiments (51.5°N) with the same clones of A. fabae and M.viciae revealed much longer critical day lengths for gynopara and male induction in A. fabae compared with those in the laboratory, but the same critical day length for ovipara induction in M.viciue. Minimal night temperatures in the field were on average 6°C, whereas maximal day temperatures declined from around 30°C in early September to 12°C at the end of October; it seems that the critical day lengths in A.fabae are temperature dependent, whereas the findings for M.viciae confirm that the critical day length is temperature compensated.     

Induction and inhibition of diapause by the same photoperiod: experimental evidence for a "double circadian oscillator clock"

On the southern Iberian Peninsula, the seasonal life history of the large white butterfly, Pieris brassicae, comprises 2 different photoperiodically induced developmental arrests: a hibernation diapause at photophases < 11 h and an estivation diapause at photophases > 14 h. At intermediate photophases (12 h to 13 h), the butterfly responds with a nondiapause. Combined with the experimental setup to determine photosensitivity in insects, the different photoperiodic responses at long-, intermediate-, and short-night conditions were examined to gain more insight into the time measurement mechanism in P. brassicae. The study reveals evidence for a "double circadian oscillator clock" mechanism that is based on 2 submechanisms, a "short-night determining system" and a separate "long-night determining system." This conclusion was drawn from the facts that an LD 9:15 long-night induces a hibernation diapause but inhibits an estivation diapause and, conversely, that an LD 16:8 short-night inhibits a hibernation diapause but induces an estivation diapause. This opposite effect of the same photoperiod supports the argument for the existence of 2 independent targets for light-dark cycles, interpreted as 2 antagonistic time measurement systems. The existence and independence of 2 systems was further shown by differences in long-night versus short-night responses regarding photosensitivity, temperature dependence, and heritable factors. The long-night measurement system is most effective in the 5th larval stage, is highly affected by temperature, and is easy to manipulate by selective inbreeding. The short-night measurement system is most effective in the 4th larval stage, is largely temperature compensated, and is not affected by experimental manipulation of the longnight measurement system.     

Photoperiodic control of diapause in Pseudopidorus fasciata (Lepidoptera: Zygaenidae) based on a qualitative time measurement

In the zygaenid moth, Pseudopidorus fasciata, both larval diapause induction and termination are under photoperiodic control. In this study, we investigated whether photoperiodic time measurement (with a 24-h light-dark cycle) in this moth is qualitative or quantitative. Photoperiodic response curves, at 22, 25, and 28 degrees C indicated that the incidence of diapause depended on whether the scotophases exceeded the critical night length (CNL) or not. All scotophases longer than the CNL-induced diapause; all scotophases shorter than the CNL-inhibited diapause. The CNL was 10.5h at 25 and 28 degrees C, and 10h at 22 degrees C. By transferring from various short photoperiods (LD 8:16, LD 9:15, LD 10:14, LD 11:13, LD 12:12, and LD 13:11) to a long photoperiod (LD 16:8) at different times, the number of light-dark cycles required for 50% diapause induction at 25 degrees C was 7.14 at LD 8:16, 7.2 at LD 9:15, 7.19 at LD 10:14, 7.16 at LD 11:13, and 7.13 at LD 12:12, without showing a significant difference between the treatments. Only at LD 13:11 (near the CNL), the number of light-dark cycles was significantly increased to 7.64. The intensity of diapause induced under different short photoperiods (LD 8:16, LD 9:15, LD 10:14, LD 11:13, and LD 12:12) at 25 degrees C was not significantly different with an average diapause duration of 36 days. The duration of diapause induced under LD 13:11 was significantly reduced to 32 days. All results indicate that the night-lengths are measured as either "long" or "short" compared with some critical value and suggest that photoperiodic time measurement for diapause induction in this moth is based on a qualitative principle.     

Diapause induction and clock mechanism in the cabbage beetle, Colaphellus bowringi (Coleoptera: Chrysomelidae)

Photoperiodic control of diapause induction was investigated in the short-day species, Colaphellus bowringi, which enters summer and winter diapause as adult in the soil. Photoperiodic responses at 25 and 28 degrees C revealed a critical night length between 10 and 12 h; night lengths > or =12 h prevented diapause, whereas night lengths <12 h induced summer diapause in different degree. Experiments using non-24-h light-dark cycles showed that the duration of scotophase played an essential role in the determination of diapause. Night-interruption experiments with T=24 h showed that diapause was effectively induced by a 2-h light pulse in most scotophases; whereas day-interruption experiments by a 2-h dark break had a little effect on the incidence of diapause. The experiments of alternating short-night cycles (LD 16:8) and long-night cycles (LD 12:12) during the sensitive larval period showed that the information of short nights as well as long nights could be accumulated. Nanda-Hamner experiments showed three declining peaks of diapause at 24 h circadian intervals. Bünsow experiments showed two very weak peaks for diapause induction, one being 8 h after lights-off, and another 8 h before lights-on, but it did not show peaks of diapause at a 24 h interval. These results suggest that the circadian oscillatory system constitutes a part of the photoperiodic clock of this beetle but plays a limited role in its photoperiodic time measurement.     

Photoperiodic clock of diapause induction in Pseudopidorus fasciata (Lepidoptera: Zygaenidae)

Pseudopidorus fasciata enters diapause as fourth instar larvae at short day lengths. Using 24-h light-dark cycles, the photoperiodic response curves in this species appeared to be similar with a critical night length of 10.5h at temperatures below 30 degrees C. At an average temperature of 30.5 degrees C, the critical night length had shifted to between 15 and 17h. In experiments using non-24-h light-dark cycles, it was clearly demonstrated that the dark period (scotophase) was the decisive phase for a diapause determination. In night interruption experiments using 24-h light-dark cycles, a 1-h light pulse at LD12:12 completely reversed the long night effect and averted diapause in all treatments. At LD 9:15 light pulses of 1-h, 30- or 15-min also averted diapause effectively when both the pre-interruption (D(1)) or the post-interruption scotophases (D(2)) did not exceed the critical night length. If D(1) or D(2) exceeded the critical night length diapause was induced. The most crucial event for the photoperiodic time measurement in this species is the length of the scotophase. A 10-min light pulse placed in the most photosensitive phase reversed diapause in over 50% of the individuals. Night interruption experiments under non-24-h light-dark cycles indicated that the photoperiodic clock measured only D(1) regardless of the length of D(2), suggesting that the most inductive cycles are often those in which L+D are close to 24h. In resonance experiments, this species showed a circadian periodicity at temperatures of 24.5 or 26 degrees C, but not at 30.5 and 23.3 degrees C. On the other hand, Bünsow and skeleton photoperiod experiments failed to reveal the involvement of a circadian system in this photoperiodic clock. These results suggest the photoperiodic clock in this species is a long-night measuring hourglass and the circadian effect found in the final expression of the photoperiodic response in the resonance experiments may be caused by a disturbing effect of the circadian system in unnatural regimes.     

Flowering requirements in Bromus inermis, a short-long-day plant

Smooth bromegrass plants ( Bromus inermis Leyss.) have a dual photoperiodic requirement for flowering. At temperatures ranging from 6 to 24°C, short days (SD) are necessary for primary induction while a transition to long days (LD) is required for initiation of flower primordia, culm elongation and flower development (secondary induction). Critical photoperiods for primary induction (50% flowering) were 13.5 h (15°C) and 12 h (24°C) in the American cv. Manchar and 14.5 and 13 h, respectively, in the Norwegian cv. Löfar. For the secondary induction the respective critical photoperiods were 14 and 15 h in 'Manchar' and 16 and 17.5 h in 'Löar', which also appeared to be better adapted to low temperatures. Low temperature vernalization in LD for up to 16 weeks at 3°C was unable to cause primary induction and temperatures below 12°C also strongly reduced the SD effect. At optimum temperature (15-2TC) 4 to 6 weeks of 8-10 h SD treatments were needed for optimal primary induction effect. A minimum of 8 LD cycles of 24 h were required for complete secondary induction in 'Manchar', while more than 16 cycles were needed in 'Löfar'. Seedlings grown in SD developed a rosette type of growth with shoots growing in a decumbent position, while those in LD grew upright and formed elongated vegetative culms. Rate of leaf initiation was enhanced by about 60% by LD while tillering was promoted by SD.     

Diapause induction and clock mechanism in the cabbage butterfly Pieris melete Ménétriés

Photoperiodic control of diapause induction was systematically investigated in the cabbage butterfly, Pieris melete, which enters summer and winter diapause as a pupa. Summer and winter diapause are induced principally by short and long scotophases, respectively; the intermediate scotophases (11-12 h) permit pupae to develop without diapause. Photoperiodic responses under 24-h light-dark cycles at 16.9, 18, 20 and 22 °C showed that the hibernation response was temperature compensated, whereas aestivation response was strongly temperature-dependent. The incidence of diapause for both aestivation and hibernation showed a decline at the ultra-short and ultra-long scotophases. Experiments using non-24-h light-dark cycles showed that the length of the scotophase played an essential role in the determination of diapause. The highest photosensitivity differed under hibernation and aestivation conditions. With a 3 × LD 12:12 interruption, a maximal inhibition of aestivation occurred in the L3/2 stage, and of hibernation it occurred in the L4/0 stage. A long-night of LD 10:14 induced hibernation diapause but inhibited aestivation diapause and, conversely, a short-night of LD 14:10 inhibited hibernation diapause but induced aestivation diapause. With a 1-h light pulse at LD 11:13, a maximal inhibition of hibernation occurred 3 h before lights-on (late scotophase), whereas, with a 1-h light pulse at LD 12.5:11.5, a maximal induction of aestivation occurred 2-3 h after the onset of darkness (early scotophase). Nanda-Hamner and Bünsow experiments failed to reveal the involvement of a circadian system, suggesting that the photoperiodic time measurement for diapause induction in this butterfly resembles an hourglass-like timer or a damped circadian oscillator.     

On critical night lengths and temperature compensation in the photoperiodic response of two geographical clones of the black bean aphid, Aphis fabae

Photoperiodic response curves were determined for two clones of the black bean aphid, Aphis fabae Scopoli, at three temperatures, 12.5, 15 and 17.5°C. Critical night lengths for the induction of winged females in an English clone (52° N) were 10.5, 11 and 11.5 h, respectively, and 10, 10.5 and 11 h in a Scottish clone (57° N). Critical night lengths for male induction were 10.5, 11 and 11 h at 12.5, 15 and 17.5°C in the English clone, and 10, 10.5 and 10.5 h, respectively, in the Scottish clone. High incidences of winged females and males were observed at all scotophases longer than the critical night length in both clones. In addition, in the English clone, the incidences of winged female and male producers in continuous darkness were 0% at 15 and 17.5°C, and 6% at 12.5°C. In the Scottish clone, however, continuous darkness resulted in high incidences of both winged female and male producers at 12.5 and 15°C, but 0% winged female producers and 6% male producers at 17.5°C. In scotophases shorter than the critical night length, including continuous light, no males or winged females were observed in either clone under the non‐crowded rearing conditions used. The results are discussed in terms of the ‘double circadian oscillator model’ for photoperiodic induction.     

Photoperiodic induction of diapause in the spider mite Tetranychus urticae: qualitative or quantitative time measurement?

Abstract. Insects and mites may measure photoperiods eitfier by classifying them as long or short relative to a critical value (qualitative time measurement) or by using the absolute value (quantitative time measurement). The spider mite Tetranychus urticae is thought to use a qualitative mechanism of time measurement. In this paper we present the results of experiments with an inbred line of the spider mite (to keep genetic variation in photoperiodic responses small), to test whether quantitative aspects also play a role. Differences in diapause incidence in different long-night photoperiods at different temperatures may be an indication of quantitative responses to photoperiod. The effect of temperature on the photoperiodic response curve was studied at 16^oC, 19^oC and 22^oC. The response curves appeared to be similar at 16^oC and 19^oC, with a critical nightlength between 10 and 11 h. At 22^oC, diapause induction was less than 100% in all long-night regimens and die critical nightlength had shifted to 12 h. Maximum diapause induction (93%) occurred in a light-dark cycle with a 16 h dark phase (LD 8:16 h). Diapause induction was lowest in long-night photoperiods with dark phases of 20 h and longer. The number of light-dark cycles needed for 50% diapause induction at 19^oC varied. between 12.1 and 14.7 for LD 6:18 h, between 10.9 and 12.5 for LD 8:16 h, between 10.6 and 11.6 for LD 10:14 h, and between 10.1 and 10.7 for LD 12:12 h. Independent of die light-dark regimen, diapause induction took place in some individuals after receiving 8 cycles and virtually all individuals entered diapause after 16 cycles. No effect was found of the photoperiodic treatment during prediapause development (LD 6:18 h, LD 8:16 h, LD 10:14 h, LD 12:12 h) on diapause duration. The average diapause duration at LD 10:14 h and 19^oC was 61 days over all four treatments. We explained the results by hypothesising that nightlengths are assessed qualitatively and mat the photoperiodic clock operates more accurately near the critical nightlength.     

Induction and termination of prepupal summer diapause in Pseudopidorus fasciata (Lepidoptera: Zygaenidae)

The seasonal life cycle of the zygaenid moth, Pseudopidorus fasciata is complicated by two different developmental arrests: a winter diapause as a fourth larval instar and a summer diapause as a prepupa in a cocoon. Both larval diapause induction and termination are under photoperiodic control. Short days induce larval diapause with a critical daylength of 13.5h and long days terminate diapause with a critical daylength of 14h. In the present study photoperiodic control of summer diapause was investigated in Pseudopidorus fasciata. Under long photoperiods ranging from LD 14:10 to LD 18:6, only part of the population entered summer diapause, the rest continued to develop. The lowest number of prepupae entered diapause at LD 14:10, followed by LD 16:8 and LD 17:7. The highest incidence of diapause occurred with photoperiods of LD 15:9 and LD 18:6. By transferring the diapausing prepupae induced by various long photoperiods (LD 14:10, LD 15:9, LD 16:8, LD 17:7, LD 18:6) to LD 13:11, 25 degrees C, the duration of diapause induced by LD 14:10 was significantly shorter than those induced by longer photoperiods. By keeping aestivating prepupae induced by LD 15:9, 28 degrees C or by natural conditions at short photoperiods (LD 11:13 and LD 13:11) and at a long photoperiod (LD 15:9), the duration of diapause at LD 15:9 was more than twice as long as than those at LD 11:13 and LD 13:11. Moreover, adult emergence was highly dispersed with a high mortality at LD 15:9 but was synchronized with low mortality at LD 11:13 and LD 13:11. When the naturally induced aestivating prepupae were kept under natural conditions, the early aestivating prepupae formed in May exhibited a long duration of diapause (mean 126 days), whereas the later-aestivating prepupae formed in July exhibited a short duration of diapause (mean 69 days). These results indicate that aestivating prepupae require short or shortening photoperiod to terminate their diapause successfully. By transferring naturally induced aestivating prepupae to 25, 28 and 30 degrees C, the duration of diapause at the high temperature of 30 degrees C was significantly longer than those at 25 and 28 degrees C, suggesting that high temperature during summer also plays an important role in the maintenance of summer diapause in Pseudopidorus fasciata. All results reveal that summer diapause can serve as a "bet hedging" against unpredictable risks due to fluctuating environments or as a feedback mechanism to synchronize the period of autumn emergence.     

Sexual forms of the pea aphid, Acyrthosiphon pisum, produced on an artificial diet

In recent years a number of aphid species have been successfully reared on chemically defined diets (Dadd & Mittler, 1966; Auclair, 1965; Dadd & Krieger, 1967; Ehrhardt, 1968). The development of such diets has offered an opportunity to study in detail several aspects of the physiology of these insects. In particular, the composition of the artificial diet has been shown to influence the production of winged forms by Myzus persicae (Sulzer) (Mittler & Dadd, 1966; Dadd, 1968). In all studies thus far, the aphids have been maintained in the parthenogenetic condition in order to accumulate data concerning the growth and fecundity of females of successive generations. However, it was clearly of interest to determine whether sexual forms could be produced by diet-reared aphids. If so, further information regarding the sexual reproduction of these insects would be forthcoming. Attempts to achieve this using local strains of Myzus persicae, Aphis fabae Scopoli and Acyrthosiphon pisum (Harris) were unsuccessful, presumably because these strains were anholocyclie (Kunkel, unpubl.). A clone of a green strain of A. pisum, previously found to be holocyclic (Sutherland, unpubl.), was then obtained from England and was cultured at 20° C in a photoperiodic regime of 16 hr light: 8 hr dark per day on young bean plants (Vicia faba). The artificial diet on which the experimental aphids were maintained was formulated according to Dadd (1967) and enclosed in sachets of stretched parafilm (Dadd, Krieger & Mittler, 1967). The aphids were provided with fresh sachets every 3–4 days. Adult apterous females taken from the plant culture were caged in groups of five, and exposed to a photoperiodic regime of 10 hr light: 14 hr dark per day at 15°. Successive batches of larvae deposited by these aphids were maintained in this environment until they were adult and had produced offspring for several days. These developed into oviparae and males. Compared to the sexual forms produced on host plants, these diet-reared individuals grew relatively poorly and mortality was high. Nevertheless, the surviving oviparae deposited numerous eggs, but these remained pale green whereas viable, fertilized eggs deposited by plant-reared oviparae rapidly become black. In the case of aphids reared on host plants in a short-day environment the possibility exists that the photoperiod may act indirectly via the plants and not directly on the insects themselves — a doubt which has been raised concerning Megoura viciae Buckton (von Dehn, 1967). However, our results with A. pisum reared on artificial diet demonstrate, as Lees did for M. viciae (Lees, 1960, 1967), that it is unnecessary to implicate the host plant in the determination of males and oviparae. This does not, of course, exclude the possibility that photoperiod-induced changes in a host plant may play a role as well. Nor have we ruled out the possibility that dietary composition may influence the aphids directly or their response to other environmental stimuli leading to the production of sexual forms.     

Photoperiodism of diapause induction in Thyrassia penangae (Lepidoptera: Zygaenidae)

Thyrassia penangae enters winter diapause as a prepupa in a cocoon. Photoperiodism of diapause induction was systematically investigated in this moth. The photoperiodic response curves under 24-h light-dark cycles showed that this insect is a typical long-day species. The critical daylength was 13 h 30 min at 25 °C, 13 h at 30 °C and 12 h 20 min at 28 °C. Transferring experiments from a short day (LD 12:12) to a long day (LD 15:9) or vice versa indicated that photoperiodic sensitivity mainly occurs during the larval period. In experiments using non-24-h light-dark cycles, when the length of photophase exceeded the critical daylength (13.5 h), was diapause inhibited effectively, even when the length of scotophase exceeded the critical nightlength (10.5 h). Only when a long scotophase was combined with a short photophase, diapause was induced effectively. This result suggests that daylength measurement is more important than nightlength measurement in T. penangae. Night interruption experiments under 24-h light-dark cycles exhibited two points of apparent light sensitivity, but the photosensitive position was highly influenced by temperature and the length of scotophase. Nanda-Hamner experiments failed to reveal the involvement of a circadian system in this photoperiodic time measurement. All light-dark cycles from LD 12:12 to LD 12:72 resulted in a short day response, and all cycles from LD 14:4 to LD 14:72 resulted in a long day response, suggesting that photoperiodic time measurement in this moth is performed by a day-interval timer or an hourglass-like clock.