The effect of temperature on the photoperiodic 'clock' and 'counter' of a Scottish clone of the vetch aphid, Megoura viciae

Photoperiodic response curves were determined for a Scottish clone of the vetch aphid, Megoura viciae Buckton, at three temperatures: 12.5, 15, and 17.5 degrees C. Critical night lengths (CNLs) for ovipara (sexual female) induction were 6 h, 7 h and 8 h, respectively. High incidences of ovipara production were observed in all night lengths longer than the CNL including continuous darkness (DD), as well as in continuous light (LL) at 12.5 and 15 degrees C. At the same three temperatures, the number of long- or short-night cycles required for half of the experimental aphids to be ovipara producers (i.e. the required day number, RDN) was determined. The RDN for long-night cycles (LD12:12) could not be determined at 12.5 degrees C, but was temperature compensated between 15 and 17.5 degrees C. The RDN for short-night cycles (LD20:4) could not be determined at any temperature. However, as induction of oviparae was always 100% in 12.5 degrees C, 94-100% in 15 degrees C and dropped from 100% to between 47 and 71% in 17.5 degrees C, it seems that short-night accumulation was temperature dependent. When fourth-stadium larvae were transferred from LD20:4 at 20 degrees C to the same light-dark cycle at 15 degrees C, the aphids, when adult, switched to the production of oviparae after about 4 weeks. First-born progeny kept in LD20:4 and 15 degrees C switched to the production of oviparae about 7 days after the moult to adult. Thus, the photoperiodic response can be directly affected by temperature, irrespective of photoperiod. Model-generated response curves using the 'double circadian oscillator model' for photoperiodic time measurement (Vaz Nunes, M., 1998. A double circadian oscillator model for quantitative photoperiodic time measurement in insects and mites. Journal of Theoretical Biology 194, 299-311) closely resembled the observations. Differences between these data and the results of previous experiments with an English clone of M. viciae could be accounted for by differences in the photoperiodic clocks (damping rate and period) as well as the photoperiodic counters.     

The influence of natural enemies on wing induction in Aphis fabae and Megoura viciae (Hemiptera: Aphididae)

Previous studies have shown that the aphid species, Aphis fabae Scopoli and Megoura viciae Buckton, do not produce winged offspring in the presence of natural enemies, in contrast to results for the pea aphid (Acyrthosiphon pisum (Harris)) and the cotton aphid (Aphis gossypii Glover); but these studies did not involve exposing aphids directly to natural enemies. We exposed colonies of both A. fabae and M. viciae to foraging lacewing (Chrysoperla carnea (Stephens)) larvae and found that the predators did not induce winged morphs among offspring compared to unexposed controls. Colonies of A. fabae responded to an increase in aphid density with increasing winged morph production, while such response was not found for M. viciae. We suggest that different aphid species differ in their susceptibility to natural enemy attack, as well as in their sensitivity to contact.     

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.     

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.     

PHOTOPERIOD IN XANTHIUM POPULATIONS FROM TEXAS AND MEXICO

Photoperiodic responses of Xanthium strumarium L. originating between 19° N in Mexico and 34° N in Texas varied among seedlings grown from seed under controlled conditions. The critical night lengths form a gradient from 9.5 hr in northern Texas to 10.75 hr in southern Texas and northeastern Mexico. Populations with critical night lengths of 9.5 and 9.75 hr showed a longer interval to flower bud formation under cooler temperatures (24 C day/15 C night) than under warmer temperatures (30 C day/24 C night). Three of four populations with a 10.75-hr critical night length showed a shorter interval under the cooler temperature regime. Although the Texas populations demonstrate a strong correlation of photoperiodic response with latitude, the Mexico populations show diverse photoperiodic timing from approximately the same latitude. The study emphasizes that a combination of critical night length and ripeness-to-flower (maturity) response forms the basis for reproductive adaptation in different climatic regimes in Texas and Mexico.     

Inheritance of photoperiodic response in the bird cherry aphid, Rhopalosiphum padi

Abstract. The photoperiodic induction of presexual females (gynoparae) and males of the aphid Rhopalosiphum padi (L.) was examined in single clones collected from different latitudes (N clone from Blair Atholl, 56.5N 3.1W; C clone from Leeds, 53.5N 1.4W and S clone from Exeter, 50.4N 3.3W). Critical night lengths (CNLs) for gynopara and male production (CNLs: 50% of maximum production) and inter-clonal differences, defined by the different forms of progeny produced at a single discriminating night length (12 h 30 min), were measured at 16 ± 1C. The aphid clones differed in CNL and in the morphs produced at the discriminating night length. These differences were used to investigate the inheritance of the photoperiodic response. In crosses between clones the photoperiodic response showed considerable overall variation. The variation in CNLs indicated that the photoperiodic response was unlikely to affect the overwintering success after long-distance movement of clones from one latitude to another.     

The identification of an aphid juvenile hormone, and its titre in relation to photoperiod

ABSTRACT. Whole body extractions from larval and adult apterous forms of Megoura viciae , and from adult Aphis fabae , were analysed for the known insect juvenile hormones (JHs) by a gas chromatography-mass spectrometric method. Low levels of JH III were detected in both aphid species, the first identification of a juvenile hormone from an homopteran insect. Although the mean titre in adult M. viciae is higher in long-day than in short-day reared insects (0.12±0.03 v. 0.04±0.01 ng/g), titres were variable and measurements overlapped. The results are discussed in the context of the hormonal control of aphid polymorphism and the question of identity of homopteran and hemipteran JH.     

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.     

Inheritance of photoperiodic induction of larval diapause in the Asian corn borer Ostrinia furnacalis

The Asian corn borer Ostrinia furnacalis (Guenée) enters facultative diapause as fully‐developed larvae in response to short‐day conditions. As a consequence of geographical variation in photoperiodic response, moths from Nanchang (28°46′N, 115°50′E) enter diapause in response to short day‐lengths (D strain), even at the high temperatures whereas moths from Ledong (18°47′N, 108°89′E) exhibit almost no diapause under the same conditions (N strain). In the present study, crosses between the two strains are used to evaluate the inheritance of diapause under different photoperiods at temperatures of 22, 25 and 28 °C. The moths, both reciprocal crosses and backcrosses, show a clear long‐day response, similar to that of the D strain, suggesting that the photoperiodic response controlling diapause in this moth is heritable. However, the critical day‐length for induction of diapause is shorter in hybrids than in the D strain. The N strain also shows a short‐day photoperiodic response at the lower temperature of 22 °C, indicating that the N strain still has the capacity to enter a photoperiodically‐induced diapause, depending on the rearing temperature. The incidence of diapause in all crosses is highest with D strain fathers or grandfathers and lowest with N strain fathers or grandfathers, indicating that the male parent has significantly more influence on the incidence of diapause of subsequent progeny than the female. The results obtained from all crosses under LD 12 : 12 h or LD 13 : 11 h photocycles at 25 °C show that inheritance of diapause in O. furnacalis does not fit an additive hypothesis and that the capacity for diapause is transmitted genetically in the manner of incomplete dominance.     

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.     

Photoperiodic induction of winged females in the black bean aphid. Aphis fabae

Abstract. The Photoperiodic of winged females (alatae) in the black bean aphid, Aphis fabae Scop. (Homopetera: Aphididae), is investigated in detail with emphasis on the interaction of the maternal and embryonic/young larval photoperiodic clocks. Previous work had shown that in uncrowded conditions the induction of gynoparae (winged females that produce sexual females) requires both prenatal and postnatal exposure to long-night (12 h) Photoperidic cycles: present results show that sole postantal exposure to long nights of any lenght does not induce wing formation in early-born aphids.
When aphids were exposed to experimental light-dark cycles postanatally only, their daughters developed as alate in long nights and as apterae in short nights: the critical night lenght (CNL) was 11:1 h. Additional prenatal exposure to experimental regimes resulted in a significantly shorter CNL (10.6 h). This difference could be accounted for by the fact that more experimental light-dark cycles were experienced in the latter case.
Apterous aphids transferred from LD 16:8 h to LD 12:12 h as either third-or fourth-stadium larvae, or young adults, switched for aptera-production to alata-production. The transition form aptera- to alata-production was rather abrupt in third-stadium transfers but more gradual when transfers occurred as fourth-stadium larvae and adults. Moreover, s the number of days required for 50% of the aphids to become alata-producers increased from 7–8 in third-stadium transfers, to 9–10 and 11–12 in the later transfers.     

The effect of temperature and light pulses on the induction of diapause in the Toyama strain of the Indian meal moth, Plodia interpunctella

Abstract.The photoperiodic response in Plodia interpunctella collected at Toyama (36.7°N) was of long-day type and highly sensitive to temperature. The critical photoperiod giving 50% diapause was between 14 and 16 h at 20°C, between 12 and 14 h at 25°C and between 6 and 8 h at 30°C. Effects of night interruption by a 2-h light pulse on the diapause response were examined at 25°C on different background photoperiods ranging from LD 12:12 h to LD 2:22 h. Percentage diapause was very low when the middle portion of dark period was interrupted, so that U- or V-shaped response curves were obtained with background scotophases longer than 12 h. In these curves, the descending slopes were less steep than the ascending slopes. The critical dark period measured from dusk to an interrupting light pulse was about 1.5 h longer than the critical dark period ( c . 10 h) in the normal photoperiodic response. The critical dark period from the interrupting light pulse to dawn, on the other hand, was not parallel to dawn but shorter than the normal critical period in LD 12:12 h and LD 10:14 h and longer than that in LD 7:17 h to LD 4:20 h, indicating that the priming effects of the light pulse might be under the influence of the photophase.     

Effects of photoperiod and temperature on diapause induction in Conogethes punctiferalis (Lepidoptera: Pyralidae)

The yellow peach moth, Conogethes punctiferalis (Guenée), a multivoltine species that overwinters as diapausing larvae, is one of the most serious insect pests on maize in China. Effect of photoperiod and temperature on larval diapause was examined under empirical laboratory conditions. Short‐day treatments caused larval diapause at 25°C, and the critical photoperiod was between 12 and 13 h (or 12 h 51 min) light per day. No sensitive instar was identified for diapause induction under alternated short‐ (L : D 11 : 13 h) and long‐day (L : D 14 : 10 h) treatments at different larval stages. However, accumulative treatment of three instars and 10 d under short‐day treatment was required for the induction of 50% larval diapause. All larvae entered diapause at 20°C, whereas less than 3% did so at 30°C, irrespective of the long‐ or short‐day treatment. Furthermore, under the short‐day treatment, more than 90% of larvae went into diapause with temperatures ≤ 25°C, but less than 17% did so at 28°C. In contrast, under the long‐day treatment, less than 19% of larvae went into diapause with temperatures ≥ 23°C. The forward shift (5°C) of critical temperature under the long‐day regime demonstrated the compensatory effect of temperature and photoperiod on diapause induction. In conclusion, C. punctiferalis had a temperature‐dependent type I photoperiodic diapause response; there was no sensitive instar for diapause determination, but the photoperiodic accumulation time countermeasures both of the short‐day cycles and the number of instars exposed, and the photoperiodic diapause response, was a temperature‐compensated phenomenon.     

Requirement for far-red light to maintain secondary needle extension growth in northern but not southern populations of Pinus sylvestris (Scots pine)

Extension growth of secondary needles is under photoperiodic control in Pinus sylvestris . To test for the effects of far-red light on maintaining this extension growth, seedlings of six populations originating from latitudes between 57° and 67°N were raised for 11 weeks in continuous incandescent (metal halogen) light at 300 µmol m⁻² s⁻¹ and 20°C and then transferred at the same temperature to a daily regime of 8 h incandescent light (230 µmol m⁻² s⁻¹) followed by a 16 h day extension with cool white fluorescent light (40 µmol m⁻² s⁻¹, R/FR ratio 7.5) or with incandescent lamps (20 µmol m⁻² s⁻¹, R/FR ratio 2.0). For the seedlings from the three populations north of 64°, needle extension growth over 42 days in the FR-poor day extension treatment was lower by up to 40% than in the FR-rich day extension treatment, whereas for the seedlings from the three southern populations the needle extension growth was similar in both day extension treatments. The requirement for FR in day extensions is characteristic of 'light-dominant' photoperiodic control mechanisms. It appears that P. sylvestris changes from dark-dominant night timekeeping to light-dominant day timekeeping with increasing latitude, as with the photoperiodic control of budset in Picea abies .     

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.     

Effects of thermoperiods on the reproductive activity of females and on the maternal induction of larval diapause in the blowfly, <Emphasis Type="Italic">Calliphora vicina</Emphasis> R.-D. (Diptera,Calliphoridae)

The interaction of thermoperiod and photoperiod in their influence on the reproductive maturation of females and on the induction of the maternal effect determining larval diapause of the progeny of the blowfly, Calliphora vicina, was first investigated under laboratory conditions. Under the combination of a day length of 12 h with a thermoperiod (the alternation of 12 h long periods with temperatures of 10 and 20°C) the reproductive maturation of females was faster than at the corresponding mean constant temperature of 15°C. Under the “natural” thermoperiod, when the period with a temperature of 10°C coincided with “night-time” (the dark phase of the diurnal light-dark cycle) the maturation of females was slower than that under the “inverted” thermoperiod, when the period with a temperature of 10°C coincided with “day-time” (the light phase of the diurnal light-dark cycle). The proportion of diapausing individuals was maximal in the progeny of females kept at 20°C and decreased with the increase in temperature. Under thermoperiods (the alternations of 12 h long periods with temperatures of 20 and 26°C) the proportion of diapausing progeny was lower than that under the corresponding mean constant temperature of 23°C, but under the inverted thermoperiod with a high night temperature this effect was much stronger. In combination with the results of our previous studies, these data support the hypothesis that the effects of “night” and “day” temperatures are substantially different only when the thermal response interacts with a strong photoperiodic response.     

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.     

白蛾周氏啮小蜂滞育诱导及滞育后发育

本研究针对人工繁育白蛾周氏啮小蜂Chouioia cunea Yang过程中出现的小蜂滞育现象, 对其滞育诱导的光周期反应及敏感光照虫态进行了调查。结果表明: 沈阳地区的白蛾周氏啮小蜂属长日照型昆虫, 以老熟幼虫进入滞育状态, 但在不同的温度条件下诱导滞育的临界光周期不同, 在18℃时诱导滞育的临界光周期处于13L∶11D和14L∶10D之间; 在21℃和24℃时诱导滞育的临界光周期变短, 处于12L∶12D和13L∶11D之间。白蛾周氏啮小蜂滞育诱导的敏感光照虫态为幼虫期, 且以幼虫的后期最为敏感, 但整个幼虫期接受短光照对滞育的形成更为有利。通过观察白蛾周氏啮小蜂滞育后在18℃, 21℃, 24℃和30℃的恒温条件下的发育历期, 由最小二乘法计算出白蛾周氏啮小蜂老熟幼虫滞育后发育起点温度和有效积温分别为14.60±0.31℃和209.38±8.72日·度。这些结果可为进一步研究白蛾周氏啮小蜂的种蜂长期保存技术和指导商品蜂生产, 正确把握放蜂时机提供理论依据。     

Effect of temperature on development rate and fecundity of apterous Aphis gossypii Glover (Hom., Aphididae) reared on Gossypium hirsutum L.

The developmental time, survival and reproduction of the cotton aphid, Aphis gossypii Glover (Hom., Aphididae), were evaluated on detached cotton leaves at five constant and two alternating temperatures (15, 20, 25, 30, 35, 25/30, and 30/35°C). The developmental periods of the immature stages ranged from 12.0 days at 15°C to 4.5 days at 30°C. A constant temperature of 35°C was lethal to the immature stages of A. gossypii. The lower developmental threshold for the cotton aphid was estimated at 6.2°C and it required 108.9 degree-days for a first instar to become adult. The average longevity of adult females was reduced from 39.7 days at 15°C to 12.6 days at 30/35°C. The average reproduction rate per female was 51.5 at 25/30°C and 20.9 at 30/35°C. Mean generation time of the population ranged from 10.4 days at 30°C to 24.5 days at 15°C. The largest per capita growth rate ( r _m = 0.413) occurred at 30°C, the smallest at 15°C ( r _m = 0.177). It was evident that temperatures over 30°C prolonged development, increased the mortality of the immature stages, shortened adult longevity, and reduced fecundity. The optimal range of temperature for population growth of A. gossypii on cotton was 25/30–30°C.     

The sensitivity of larval Plodia interpunctella and Ephestia elutella (Lepidoptera) to light during the photoperiodic induction of diapause

ABSTRACT. The incidence of diapause in larvae of Plodia interpunctella and Ephestia elutella held under two light systems was examined. Both systems progressively shortened the photophase of 24-h cycles, one with a motorized dimming switch providing dawns and dusks about 1 h long, the other switching the lights instantaneously. The mean critical photoperiod for P. interpunctella was about 131/4 h and for E. elutella just over 14 h. In both species light intensities as low as 0.2 lx influenced the induction of diapause. In P. interpunctella the critical photoperiod and sensitivity to light were similar at 23.±.;5°C and 20.5±0.5°C. At 22.5°C the percentage of diapausing larvae of E. elutella increased from 2% in long photoperiods (> 15 h light), to 100% in short photo-periods (t 12.5h light). Fox P. interpunctella , at 22.5°C the percentage increased from zero in long photoperiods (> 14 h light) to about 98% in short photoperiods (< 11.5h light), and at 20°C from 12% to 100% over a similar photoperiodic range. Similar results were obtained under selected fixed photoperiods, switched on or off instantaneously.