Abstract
Timing seasonal events, like reproduction or diapause, is crucial for the survival of many species. Global change causes phenologies worldwide to shift, which requires a mechanistic explanation of seasonal time measurement. Day length (photoperiod) is a reliable indicator of winter arrival, but it remains unclear how exactly species measure day length. A reference for time of day could be provided by a circadian clock, by an hourglass clock, or, as some newer models suggest, by a damped circadian clock. However, damping of clock outputs has so far been rarely observed. To study putative clock outputs of Acyrthosiphon pisum aphids, we raised individual nymphs on coloured artificial diet, and measured rhythms in metabolic activity in light-dark illumination cycles of 16:08 hours (LD) and constant conditions (DD). In addition, we kept individuals in a novel monitoring setup and measured locomotor activity. We found that A. pisum is day-active in LD, potentially with a bimodal distribution. In constant darkness rhythmicity of locomotor behaviour persisted in some individuals, but patterns were mostly complex with several predominant periods. Metabolic activity, on the other hand, damped quickly. A damped circadian clock, potentially driven by multiple oscillator populations, is the most likely explanation of our results.
Similar content being viewed by others
Introduction
The environment cycles in a daily manner due to the earth’s rotation around its own axis. In order to cope with these rhythmic changes, organisms rely on endogenous circadian clocks. Clocks drive behavioural and physiological rhythms with periods of approximately 24 h, and thus align the organism with the environmental rhythm1,2. These rhythms persist even without environmental time cues (Zeitgebers) such as light or temperature3. Therefore, circadian clocks enable organisms not only to react to, but also to predict environmental oscillations, which may be adaptive4. Hence, circadian clocks play an important role in coping with daily environmental changes.
Circadian timekeeping might also be involved in the photoperiodic calendar and control of diapause induction, although this hypothesis is still under discussion5,6. Bünning proposed that the circadian clock forms the basis of photoperiodism7, and this idea was later formalized as external8 and internal9 coincidence models. In contrast, Lees did not observe any circadian pattern in the photoperiodic reaction of aphids and excluded therefore the involvement of a circadian oscillator. He proposed an hourglass mechanism instead, in which some biochemical product accumulates during night, so that only sufficiently long nights can trigger a photoperiodic response10,11. But some phenomena of long night experiments cannot be explained by an hour-glass mechanism, and a model with a damping circadian oscillator describes diapause induction better12. By rephrasing the hour-glass mechanism as a damping oscillator, the model unites these apparently contrary views13. However empirical data demonstrating the actual damping of circadian oscillations is largely lacking.
Aphids are central to the discussion about photoperiodic clock involvement. During summer the insect produces offspring via parthenogenesis, thereby ensuring quick population growth. In autumn sexual morphs are induced, which produce cold resisting eggs able to survive winter14. The switch in reproductive modes is induced by shortening day length15,16 and, to a lesser extent, drops in temperature. This extraordinary phenotypic plasticity allows aphids to cope with seasonal changes, and is probably one reason for their global distribution. Due to the rapid population growth in summer, various species are classified as crop pests17, and climate change with associated shifts in phenology (seasonal timing) will likely exacerbate the pest pressure of aphids18. Thus, aphids are well-suited models for circadian and seasonal time-keeping, not only due to their long research history, but also because the timing matters for applied pest management.
There is ongoing interest in the circadian clock of aphids. Several behavioural studies suggest the existence of a functional circadian clock in sexual as well as in parthenogenetic aphid forms of various aphid species19,20, although the experimental protocols did not allow to investigate damping of the clock. More recently, two studies identified putative clock genes and the location of clock gene expressing neurons in the pea aphid Acyrthosiphon pisum (Harris)21,22. Unfortunately the challenge to uncouple the aphid’s activity from the plant’s influence remained unattended in most studies. Recently we described the first daily rhythms of aphids completely independent of their host plant23, but have so far not monitored aphid rhythms in constant darkness for methodological reasons.
In the present study we investigate two different outputs of the circadian clock, namely locomotor activity and metabolic activity independently of the host plant. We show that the aphid clock drives weak, but stable, circadian output rhythms in locomotion, whereas oscillations in metabolic activity dampen quickly in constant conditions.
Material and Methods
In order to investigate the circadian behaviour of aphids, we performed two experiments: First, we supplied a coloured diet and tested for rhythms in honeydew excretion. Secondly, we applied a novel method that allows constant locomotor activity monitoring of sap-sucking insects. All experiments were performed independently of the host plant on an artificial diet (based on Febvay, et al.24, 20% (w/v) sugar). The aphids were reared in a small containment and separated from the food source by a parafilm M membrane (BEMIS COMPANY INC., USA)25, so they could access the diet from below by piercing the parafilm. The artificial diet was sterile filtrated through a 0.45 µm Minisart® syringe filter (Sartorius, Germany), and all materials that came in contact with the diet were sterilized before use. For the metabolic activity experiments we reduced the diet by eight ingredients, reordered the ingredients list, and supplemented it with 1.25 mg/ml Brilliant blue FCF26.
For all experiments we used an asexual Acyrthosiphon pisum line (LL01), a green alfalfa biotype from the Lusignan area that was kindly provided by G. Febvay (INRA Lyon, France). Stock cultures were kept on Pisum sativum (L.) var. Fuego plants in climate chambers (Sanyo/Panasonic MLR-H series; 18 ± 0.5 °C, 80% ± 10% RH, LD 16:08). All statistical tests were performed in R version 3.1.127.
Metabolic activity
We measured metabolic activity simultaneously under LD 16:08 and constant darkness for eight days. We conducted the experiment in climate chambers (Sanyo MLR-352H) at 18 °C and 70% humidity under a 15000 lux fluorescent light source. We placed 100 adult aphids on freshly cut broad bean leaves. On the next day, we discarded the adults, placed 120 nymphs individually in petri dishes (∅35 mm) and fed each with 500 µl coloured artificial diet. 60 aphids were moved into DD after five hours (Zeitgeber time (ZT) 12 = 12 hours after lights on), whereas the other 60 nymphs remained in LD, but at a reduced light intensity (7200 lux). At ZT 21 (i.e., three hours before lights-on), we counted and marked all honeydew drops which have been produced so far. Thus, the aphids in DD were given 9 hours to locate the food source before the start of measurements. We then counted honeydew every 3 hours (8 measurements per day). In addition, we counted all exuviae, as moulting individuals are not expected to produce honeydew.
Four observers have been involved in taking measurements. The time schedule was allocated in a non-random order, so that each observer occupied a different time slot every day. We always measured the replicates in the same order and timeframe. Measurements in the light phase were conducted under room light while measurements in the dark phase were made under red LED light. The excreted blue honeydew drops were equally visible under both light conditions.
The first half of the replicates in the LD treatment was removed from the experiment, because they were accidentally taken into room-light during lights-out in the first night. Hence, sample sizes were 30 in LD and 60 in DD. Because we did not renew the diet during the experiment in order to reduce disturbance, petri dishes became contaminated during the experiment and were subsequently removed. Thus, sample sizes decreased over time, with 80% of the samples remaining for at least 5 days. In LD sample size decreased in total from 30 to 14, and in DD from 60 to 17.
Only 3.4% of the aphids produced more than one honeydew drop in the observed time interval of three hours, so we treated the response as binomial. To test for metabolic rhythmicity, we applied a generalized linear mixed-effects model with binomial error distribution28 with the fixed factors “time of day” and “day”, and with the random term (“time of day” | “ID”). For the DD treatment, we expected the effect to dampen over the course of the experiment, so we incorporated a change in effect size over time. Hence, we used the fixed factor “time of day”, interacting with the continuous variable “time since start”, and the random term (“time of day” | ID). We checked all models for overdispersion. Because p-values are not reliable for GLMMs29, we report only confidence intervals30 for all models.
Honeydew production was infrequently interrupted by moulting, usually three times per individual. Thus, the aphids were in the final larval stage at the end of the experiment. To test whether moulting individuals produce less honeydew, we pooled all time points and applied a chi-square test of goodness of fit (2 × 2 contingency table: drop production vs moulting). Because moulting individuals indeed produced less honeydew (see results), we repeated the analysis with a reduced dataset that included only non-moulting individuals (6% of all measurements removed). In addition, we tested whether moulting itself was rhythmic, using the same model as for honeydew production in LD.
Locomotor activity
For the locomotor activity experiments we used one day old offspring of aphids that were raised on plants and then kept on artificial diet for one day in order to control for age. We adapted the DAM2 (Drosophila Activity Monitor) (Trikinetics, USA), which monitors locomotor activity via an infrared-light barrier (IR-beam), to aphid specific requirements (Fig. 1). Aphids were provided with food ad libitum in a shortened micropipette tip (volume 1000 µl) on top of the monitor tube (∅7 mm) while the activity monitors were located horizontally. We positioned the IR-beam directly under the micropipette tip and limited the animals roaming space to 1 cm. The setup allowed monitoring 32 aphids simultaneously. All animals were entrained as nymph to an LD 16:08 regime (16 hours light and 8 hours darkness) for at least 12 days. A light intensity of 200–400 lux was produced by white light LEDs (depending on the position of the monitor tube) in the light phase and 0 lux in the dark phase while temperature and humidity were kept constant (18 ± 0.5 °C, 80% ± 10% RH) in the climate chamber (Percival INTELLUS, CLF Plant Climatics GmbH, 86637 Wertingen, Germany). On day 13 one treatment group (32 aphids) was released into constant DD conditions whereas another group of 32 aphids received LD conditions throughout their life.
Activity data was recorded in beam crosses per minute and evaluated with the ImageJ software plugin ActogramJ31 (Fiji ImageJ Version 1.49, © Wayne Rasband, National Institutes of Health, USA). We calculated the average day activity profile and mean activity in light and dark phase with the activity data of several consecutive days in Microsoft Excel (2013 Microsoft Office) and day activity was tested with Wilcoxon rank sum test. We excluded days 8–12, as earlier trials have shown that aphids undergo their last moulting in this time. It was impossible to appoint the aphids to either nymph or adult status reliably during this period without interrupting data acquisition.
We tested for rhythmicity in activity of individual adult aphids across at least five consecutive days in entraining (LD) and free-running (DD) conditions with Lomb-Scargle (LS) and chi-square periodogram (CS) analysis (period 1140–1740 minutes; smoothing factor 10 (only in chi-square method); p-level 0.05). In case of several narrow spikes that barely exceeded the significance level, we appointed the periodogram as false positive and the animals as arrhythmic (see definition in32). Differences in the groups “arrhythmic”, “rhythmic” (with simple circadian rhythms) and “complex” (with complex rhythms) between LD and DD conditions were tested with Fisher’s exact test. Individuals that did not undergo all four moultings were excluded from analysis.
Data availability
All data generated or analysed during this study are included in this published article (and its Supplementary Information files). This includes R - scripts for analysis and figure reproduction of the metabolic activity experiment.
Results
Metabolic activity: Bimodal rhythmicity profile under LD and DD
We monitored metabolic activity of individual aphids over a period of eight days, by counting the number of exuviae and of visibly coloured honeydew drops every three hours. The aphids moulted three times during the eight days of measurement, on average after 24 (±3.25), 71 (±3.21) and 127 (±4.19) hours (days 1, 3 and 6). In total, we observed 252 of the expected 270 occurrences of moulting, because some aphids died during the course of the experiment. These occurrences of moulting suppressed honeydew excretion, because only 13.75% of the moulting individuals in LD produced honeydew drops, compared to 33.76% of the non-moulting individuals (χ² = 13.75, p < 0.001). In DD 18.13% of the moulting, and 29.41% of the non-moulting individuals excreted honeydew (χ² = 9.38, p < 0.01). We therefore excluded moulting individuals from the analysis of honeydew excretion. Moulting itself was not rhythmic, neither in LD nor in DD (not shown).
The aphids which did not moult produced on average 2.7 drops per day in LD and 2.4 drops per day in DD (1230 drops in total). The data for LD conditions was best described with a model that only incorporates ‘time of day’ and ‘day’ (Fig. 2A; AIC = 1736), because the inclusion of a damping component (‘time of day’ * ‘time’ interaction) estimated more parameters but did not significantly improve the model fit (AIC = 1752). Using the ‘Effects’ package, we isolated the factor of interest, ‘time of day’, while keeping the other elements (individual variance and day of experiment) constant (Fig. 2B). This procedure is akin to calculating an average day for an average individual, and allows calculating confidence intervals (CI). This plot shows that honeydew production was markedly rhythmic under LD conditions and peaked twice during day-time (ZT 0: mean 0.42, CI 0.34–0.51; ZT 9: mean 0.45, CI 0.37–0.54) and lowest activity at night time (ZT 18: mean 0.19, CI 0.13–0.27 drops). Activity appeared to be bimodal, though the confidence intervals overlap.
Under constant darkness the model with an interaction term (damping) was better suited (AIC = 3219) than the simpler model without damping (AIC = 3222). Honeydew excretion was rhythmic during the first days (day 1, peak at 20h after lights-off: mean 0.63, CI 0.51–0.75 drops; trough at 29h after lights-off: mean 0.24, CI 0.15–0.35 drops), but the only discernible peak damped quickly and disappeared after three days (Fig. 2C,D).
We decided to measure moulting mainly because it causes aphids to stop moving for longer time periods33, and thus disrupts the activity in the young aphids. By removing moulting individuals from the analysis of metabolism, we corrected for these gaps in activity. The disruption by moulting was more severe in our measures of locomotor activity. Therefore we considered metabolic activity of nymphs, but locomotor activity of adults for analysis of circadian rhythmicity.
Locomotor activity: diurnal rhythms in LD and complex rhythms in DD
We monitored locomotor activity rhythms of aphids during their whole live from nymphal stage L1 onward in a novel monitoring set up (Fig. 1). Both nymphs (age: 1–7 days; Fig. 3A) and adult aphids (age: 13–23 days; Fig. 3B) showed significantly higher average activity during the light phase than during the dark phase (p(nymphs) < 0.05, p(adult) < 0.05, paired Wilcoxon signed rank test). The activity patterns of the aphids were, however, disrupted by activity breaks lasting entire days during the first 9 days of their life (Fig. 4A/B), leading to lower activity levels in nymphs (0.08 ± 0.02 counts/min) than in adult aphids (0.31 ± 0.07 counts/min). The latter displayed two main activity bouts that were best visible in the average day, one after lights-on the other in the late light phase (Fig. 3B). In between the two activity bouts activity levels were lower.
While we detected diurnal rhythms in activity of adult aphids in LD, they appeared largely arrhythmic under constant conditions, at least in the average actogram (Fig. 4A/B). Nevertheless, averaging concealed the temporal and inter-individual variation, so we supplement our analysis with an individual-based approach. We found that many of the adult subjects (67%) showed no activity at all during the first three days after switching to constant conditions of DD at day 13 (Fig. 4B). We therefore selected periods of at least 5 continuous days with activity, and determined the percentage of rhythmic adults (from day 13 on) in LD and DD conditions via periodogram analysis (Lomb-Scargle (LS) method in Fig. 4C and chi-square (CS) method in Fig. 4D). In DD (N = 15) 0% (CS) to 13% (LS) of the aphids were rhythmic with a single peak in the periodogram and further 80% (CS: 53%) displayed complex rhythms with more than one significant predominant period. In LD (N = 15) 60% (67% with CS method) were rhythmic with one periodogram peak and 33% (both methods) showed complex rhythmicity. Although the percentage of arrhythmic individuals was significantly higher with the CS method in DD conditions (p < 0.01, Fisher’s exact test), the results of both analysis methods are similar, as the difference in rhythmic individuals between light treatments was significant in both tests (LS: p < 0.05; CS: p < 0.01, Fisher’s exact test).
Discussion
By combining measurements of aphid honeydew production and locomotor activity, we find that aphid activity is bimodal under LD conditions. In constant darkness the rhythm persists initially, but then dampens quickly and individuals display complex rhythmicity.
We adapted a commercially available measurement system for locomotor activity of flies to monitor aphid rhythms with high data throughput. This novel monitoring method provides the first measurements of aphid locomotor activity rhythms independent of the host plant. It was sensitive enough to monitor adult aphids as well as nymphs, though the general activity level was lower than in most other insect species. For example Drosophila melanogaster 34, Musca domestica 35 and Apis mellifera 36 are approximately 10 times more active than the aphids in our locomotion setup. This finding can partly be explained by the unusual food source, which is known to compromise performance17. The aphids produced on average 2.5 honeydew drops per day, which is lower than the 4–8 drops/day reported in studies on plants37. On the other hand, different linden bug (Pyrrhocoris apterous) strains, which are of the same order (Hemiptera) and also feed by sucking, show similarly low activity levels38. Thus, the low locomotor activity levels might be related to the sap-sucking feeding behaviour.
Despite the low activity levels, aphids were clearly day active in both metabolism and locomotion. These results are in line with various studies that detected diurnal activity of aphids on plants20,39,40 as well as independently of the host plant23. Furthermore, aphids were shown to find their host plants more effectively in day light conditions41,42, indicating adaptation to a diurnal lifestyle.
The activity appeared bimodal in both behaviours with one peak around the time of lights-on and another one in the late light phase. Bimodal patterns of activity were described in a variety of different animals, for example fruit flies43, mosquitoes44, birds and rodents45, and have been linked to multi-oscillator systems46.
In the metabolic activity profile there is only one activity peak left in DD, which is probably due to a melting of the separate peaks like it has been observed in Drosophila melanogaster activity43. This peak damped quickly during the first 3–4 days in constant conditions. The observed damping of circadian rhythms could either be due to desynchronization of individual persisting rhythms or damping of individual rhythms, but the low number of honeydew drops and the resulting binomial data make it difficult to assess damping on the individual level. We thus incorporated inter-individual variation in a mixed-effects model to exclude population-level damping. The model is constrained in that the period length is fixed at 24 h, but we find it unlikely to affect our conclusions, given the 3-hour intervals of the data.
The results from locomotor activity are similar: As in the metabolic activity assay, the aphids showed clearly rhythmic behaviour in LD, and rhythmicity also persisted in DD, as the majority of individuals (LS: 93%, CS: 53%) remained rhythmic. This indicates that the behaviour is governed by the circadian clock. In contrast to the metabolic activity essay we found, however, no damping of rhythms, but instead the activity patterns transformed into complex rhythms in DD. Admittedly, most individuals in the locomotor assay were not active at all in the first few days in constant conditions, so we cannot exclude that the rhythmicity damped to some extent during the first days.
At the moment we can only speculate about the mechanisms that give rise to complex rhythms and individual level damping in DD. Complex rhythms are not unusual, and have been described before for example in mosquitoes44 and New Zealand Weta47. Lewis and co-authors proposed a two population model of circadian oscillators, driving different output rhythms. In this model different clock neuron populations in the oscillator are weakly coupled and oscillations driven by them become asynchronous in DD. Therefore different free running periods (FRPs) for the oscillator subgroups are detected, which creates complex rhythms as well as a damping in one circadian output rhythm, and eventually arrhythmicity on the individual and/or population level. We find this model appealing for aphid clocks, because it simultaneously explains the damping in one output and complex rhythms in the other output. Moreover, the model provides an explanation why some studies found clear circadian patterns19, whereas other studies with different outputs indicate hour-glass mechanisms15. Further studies on the molecular organization of the clock are needed to verify this model.
Moreover, since aphids produce honeydew during feeding and therefore metabolic and locomotor activity is directly connected, it is likely that similar mechanisms operate for these two outputs. Like the complex rhythms in locomotor activity might lead to dampened rhythmicity of the individual, damping of metabolic activity could occur at the individual level. Overall we found complex circadian rhythms in locomotion and quick damping in metabolism, and we argue that the aphid circadian clocks cannot drive strong activity rhythms.
Aphids played a central role in the development of the hourglass mechanism of the endogenous clock, which Lees postulated for the diapause induction of aphids10,11. Lees found no circadian involvement in diapause induction, causing him to question the coincidence models.
However, various aphid behaviours were found to be controlled by a circadian oscillator. For example clock gene homologues have recently been characterized, and their mRNA was shown to cycle21,22. On the behavioural level the circadian clock was shown to govern the release of aphid sex pheromone19, and fresh weight-gain and larviposition20. In the latter experiment, aphids were disrupted by shifting the light phase and the rhythms needed more than 3–4 days to re-entrain to the new conditions, which led the authors to the conclusion that this behaviour is governed by a circadian oscillator.
As an alternative model to the hour-glass model, the circadian oscillator model with damping rhythms48 can simulate the “hour-glass reaction” observed in diapause induction of aphids. However, although this model fits to the data of Lees, only recently actual damping of circadian rhythms in aphids has been demonstrated21. In this study the cycling of mRNA levels extracted from whole mount aphid brains appeared to rapidly dampen in constant conditions. Although whole mount extracts provide only a population perspective and the animals were not kept independently of the host plant, these results point to a damped circadian clock in aphids. Our study adds the analysis of output rhythms independently of the host plant and supports the model of an oscillator driving damping circadian rhythms in two points.
Firstly we observe circadian oscillations in behaviour and metabolic activity in DD, which would not be the case if the aphid endogenous clock would have an hourglass mechanism. Secondly, we see a clear damping of activity rhythms in the first few days in constant conditions, at least in metabolic activity. Hence, our study provides a first empirical evidence for a damping oscillation in aphid activity.
Though anticipating daily reoccurring events is an advantage, an oscillator that drives strong circadian rhythms over a long time is potentially less flexible in resetting to seasonal changes. There are environmental situations on earth that require organisms to adapt to extreme deviations from daily rhythms. For example reindeer living in polar regions have been found to be arrhythmic during extreme illumination conditions of the arctic summer and winter49,50,51. This adaptation enables those animals to optimally use the short season for gaining resources and hence show a strong seasonal rhythm in locomotor and metabolic activity. A similar seasonal adaptation of the circadian system has been found in Drosophila species, D. montana, D. ezoana and D. littoralis, living in Northern Europe52,53,54. Unlike D. melanogaster, which has shallow photoperiodic diapause induction55, these flies are exposed to extreme photoperiods and evolved a very robust diapause induction, while they have poor circadian activity rhythms in constant conditions. We can certainly draw here parallels to our results on aphid rhythmicity. Like the polar reindeer or the Northern Drosophila species, aphids exhibit very weak circadian rhythms, while the seasonal response to shortening photoperiod is highly robust.
The weak circadian response in aphids might be the reason why most interest so far was put on the investigation of photoperiodism while the circadian clock remained widely unattended. But this way a complete picture of clock output characteristics was missing. Our study demonstrates that the investigation of different outputs, by combining expert knowledge of different disciplines is important to gain a better understanding about properties of the aphid circadian clock. There is an ongoing discussion whether the circadian clock and the annual photoperiodic clock are two independent timing systems or if they are at least partially the same5,6. While our study offers no direct causal link between damping activity rhythms and photoperiodism, it provides the tools of measuring two different clock outputs that could be used in future experiments with varying photoperiods. Further investigation of the circadian clock in aphids, also on the molecular level, might provide us with a deeper understanding of the potential involvement of the circadian system in seasonal timing.
References
Allada, R. & Chung, B. Y. Circadian organization of behavior and physiology in. Drosophila. Annu. Rev. Physiol. 72, 605–624, https://doi.org/10.1146/annurev-physiol-021909-135815 (2010).
Mohawk, J. A., Green, C. B. & Takahashi, J. S. Central and peripheral circadian clocks in mammals. Annu. Rev. Neurosci. 35, 445–462, https://doi.org/10.1146/annurev-neuro-060909-153128 (2012).
Roenneberg, T., Daan, S. & Merrow, M. The art of entrainment. J. Biol. Rhythms 18, 183–194, https://doi.org/10.1177/0748730403253393 (2003).
Vaze, K. M. & Sharma, V. K. On the adaptive significance of circadian clocks for their owners. Chronobiol. Int. 30, 413–433, https://doi.org/10.3109/07420528.2012.754457 (2013).
Danks, H. V. How similar are daily and seasonal biological clocks? J. Insect Physiol. 51, 609–619, https://doi.org/10.1016/j.jinsphys.2005.01.005 (2005).
Kostal, V. Insect photoperiodic calendar and circadian clock: Independence, cooperation, or unity? J. Insect Physiol. 57, 538–556, https://doi.org/10.1016/j.jinsphys.2010.10.006 (2011).
Bünning, E. Die endogene Tagesrhythmik als Grundlage der photoperiodischen Reaktion. Ber. Deut. Bot. Ges. 54, 590–607 (1936).
Pittendrigh, C. S. & Minis, D. H. The entrainment of circadian oscillations by light and their role as photoperiodic clocks. Am. Nat. 98, 261–294, https://doi.org/10.1086/282327 (1964).
Pittendrigh, C. S. Circadian surfaces and diversity of possible roles of circadian organization in photoperiodic induction. Proc. Natl. Acad. Sci. USA 69, 2734–2737, https://doi.org/10.1073/pnas.69.9.2734 (1972).
Lees, A. D. Photoperiodic time measurement in the aphid Megoura viciae. J. Insect Physiol. 19, 2279–2316, https://doi.org/10.1016/0022-1910(73)90237-0 (1973).
Lees, A. D. Some effects of temperature on the hour glass photoperiod timer in the aphid Megoura viciae. J. Insect Physiol. 32, 79–89, https://doi.org/10.1016/0022-1910(86)90160-5 (1986).
Vaz Nunes, M. & Hardie, J. Circadian rhythmicity is involved in photoperiodic time measurement in the aphid Megoura viciae. Experientia 49, 711–713, https://doi.org/10.1007/BF01923957 (1993).
Saunders, D. S., Bünning, E. & Lees, T. Two giants of chronobiology, and the problem of time measurement in insect photoperiodism. J. Insect Physiol. 51, 599–608, https://doi.org/10.1016/j.jinsphys.2004.12.002 (2005).
Simon, J.-C., Rispe, C. & Sunnucks, P. Ecology and evolution of sex in aphids. Trends Ecol. Evol. 17, 34–39, https://doi.org/10.1016/s0169-5347(01)02331-x (2002).
Lees, A. D. The role of photoperiod and temperature in the determination of parthenogenetic and sexual forms in the aphid Megoura viciae Buckton—I. J. Insect Physiol. 3, 92–117, https://doi.org/10.1016/0022-1910(59)90024-1 (1959).
Marcovitch, S. Plant lice and light exposure. Science 58, 537–538, https://doi.org/10.1126/science.58.1513.537-a (1923).
van Emden, H. F. & Harrington, R. Aphids As Crop Pests. (Cabi, 2007).
Bell, J. R. et al. Long-term phenological trends, species accumulation rates, aphid traits and climate: five decades of change in migrating aphids. J. Anim. Ecol. 84, 21–34, https://doi.org/10.1111/1365-2656.12282 (2015).
Eisenbach, J. & Mittler, T. E. An aphid circadian rhythm: Factors affecting the release of sex pheromone by oviparae of the greenbug. Schizaphis graminum. J. Insect Physiol. 26, 511–515, https://doi.org/10.1016/0022-1910(80)90125-0 (1980).
Hodgson, C. J. & Lane, I. R. Some effects of photoperiod on larviposition and fresh weight-gain in Myzus persicae. Physiol. Entomol. 6, 21–25, https://doi.org/10.1111/j.1365-3032.1981.tb00256.x (1981).
Barbera, M., Collantes-Alegre, J. M. & Martinez-Torres, D. Characterisation, analysis of expression and localisation of circadian clock genes from the perspective of photoperiodism in the aphid Acyrthosiphon pisum. Insect Biochem. Mol. Biol. 83, 54–67, https://doi.org/10.1016/j.ibmb.2017.02.006 (2017).
Cortes, T., Ortiz-Rivas, B. & Martinez-Torres, D. Identification and characterization of circadian clock genes in the pea aphid Acyrthosiphon pisum. Insect Mol. Biol. 19, 123–139, https://doi.org/10.1111/j.1365-2583.2009.00931.x (2010).
Joschinski, J., Beer, K., Helfrich-Förster, C. & Krauss, J. Pea aphids (Hemiptera: Aphididae) have diurnal rhythms when raised independently of a host plant. J. Insect Sci. 16, 31, https://doi.org/10.1093/jisesa/iew013 (2016).
Febvay, G., Delobel, B. & Rahbé, Y. Influence of the amino acid balance on the improvement of an artificial diet for a biotype of Acyrthosiphon pisum (Homoptera: Aphididae). Can. J. Zool. 66, 2449–2453, https://doi.org/10.1139/z88-362 (1988).
Mittler, T. E. & Dadd, R. H. Studies on the artificial feeding of the aphid Myzus persicae (Sulzer)—I. Relative uptake of water and sucrose solutions. J. Insect Physiol. 9, 623–645, https://doi.org/10.1016/0022-1910(63)90008-8 (1963).
Joschinski, J. & Krauss, J. Food colouring as new possibility to study diet ingestion and honeydew excretion by aphids. Entomol. Exp. Appl. 164, 141–149, https://doi.org/10.1111/eea.12598 (2017).
R: A language and environment for statistical computing (R Foundation for Statistical Computing, Vienna, Austria, 2014).
Bates, D., Mächler, M., Bolker, B. & Walker, S. Fitting Linear Mixed-Effects Models using lme4. J. Stat. Softw. 67, 48, https://doi.org/10.18637/jss.v067.i01 (2015).
Halekoh, U. & Højsgaard, S. A Kenward-Roger approximation and parametric bootstrap methods for tests in Linear Mixed Models-The R package pbkrtest. J. Stat. Softw. 59, 32, https://doi.org/10.18637/jss.v059.i09 (2014).
Fox, J. Effect displays in R for Generalised Linear Models. J. Stat. Softw. 8, 27, https://doi.org/10.18637/jss.v008.i15 (2003).
Schmid, B., Helfrich-Förster, C. & Yoshii, T. A new ImageJ plug-in “ActogramJ” for chronobiological analyses. J. Biol. Rhythms 26, 464–467, https://doi.org/10.1177/0748730411414264 (2011).
Helfrich-Förster, C. Robust circadian rhythmicity of Drosophila melanogaster requires the presence of lateral neurons: a brain-behavioral study of disconnected mutants. J. Comp. Phys. A 182, 435–453, https://doi.org/10.1007/s003590050192 (1998).
Auclair, J. L. Feeding and excretion by the pea aphid, Acyrthosiphon pisum (Harr.)(Homoptera: Aphididae), reared on different varieties of peas. Entomol. Exp. Appl. 2, 279–286, https://doi.org/10.1111/j.1570-7458.1959.tb00441.x (1959).
Menegazzi, P., Yoshii, T. & Helfrich-Förster, C. Laboratory versus nature: the two sides of the Drosophila circadian clock. J. Biol. Rhythms 27, 433–442, https://doi.org/10.1177/0748730412463181 (2012).
McCarthy, K. et al. The effect of social isolation on locomotor activity in the Houseflies (Musca Domestica). J. Insect Behav. 28, 288–296, https://doi.org/10.1007/s10905-015-9501-9 (2015).
Beer, K., Steffan-Dewenter, I., Härtel, S. & Helfrich-Förster, C. A new device for monitoring individual activity rhythms of honey bees reveals critical effects of the social environment on behavior. J. Comp. Phys. A 202, 555–565, https://doi.org/10.1007/s00359-016-1103-2 (2016).
Auclair, J. L. Honeydew excretion in the pea aphid, Acyrthosiphon pisum (Harr.) (Homoptera: Aphididae). J. Insect Physiol. 2, 330–337, https://doi.org/10.1016/0022-1910(58)90018-0 (1958).
Pivarciova, L. et al. Unexpected geographic variability of the free running period in the linden bug Pyrrhocoris apterus. J. Biol. Rhythms 31, 568–576, https://doi.org/10.1177/0748730416671213 (2016).
Gomez, S. K., Oosterhuis, D. M., Hendrix, D. L., Johnson, D. R. & Steinkraus, D. C. Diurnal pattern of aphid feeding and its effect on cotton leaf physiology. Environ. Exp. Bot. 55, 77–86, https://doi.org/10.1016/j.envexpbot.2004.10.001 (2006).
Taylor, S. H., Parker, W. E. & Douglas, A. E. Patterns in aphid honeydew production parallel diurnal shifts in phloem sap composition. Entomol. Exp. Appl. 142, 121–129, https://doi.org/10.1111/j.1570-7458.2011.01206.x (2012).
Hardie, J. Spectral specificity for targeted flight in the black bean aphid. Aphis fabae. J. Insect Physiol. 35, 619–626, https://doi.org/10.1016/0022-1910(89)90124-8 (1989).
Narayandas, G. K. & Alyokhin, A. V. Diurnal patterns in host finding by potato aphids, Macrosiphum euphorbiae (Homoptera: Aphididae). J. Insect Behav. 19, 347–356, https://doi.org/10.1007/s10905-006-9029-0 (2006).
Helfrich-Förster, C. Differential control of morning and evening components in the activity rhythm of Drosophila melanogaster–sex-specific differences suggest a different quality of activity. J. Biol. Rhythms 15, 135–154, https://doi.org/10.1177/074873040001500208 (2000).
Clopton, J. R. Mosquito circadian and circa-bi-dian flight rhythms: a two-oscillator model. Journal of Comparative Physiology A 155, 1–12, https://doi.org/10.1007/bf00610925 (1984).
Aschoff, J. Circadian activity pattern with two peaks. Ecology 47, 657–662, https://doi.org/10.2307/1933949 (1966).
Saunders, D. S. Insect Clocks, Third Edition. (Elsevier Science, 2002).
Lewis, R. D., Bullivant, A. G. & King, V. M. A dual pacemaker model for the circadian system of the insect Hemideina thoracica. J. Interdiscipl. Cycle Res. 22, 293–309, https://doi.org/10.1080/09291019109360114 (1991).
Nunes, M. V. & Hardie, J. An instantly damping oscillator model for photoperiodic time measurement in the aphid Aphis fabae. J. Insect Physiol. 33, 831–841, https://doi.org/10.1016/0022-1910(87)90031-x (1987).
Lu, W. Q., Meng, Q. J., Tyler, N. J. C., Stokkan, K. A. & Loudon, A. S. I. A circadian clock is not required in an arctic mammal. Curr. Biol. 20, 533–537, https://doi.org/10.1016/j.cub.2010.01.042 (2010).
van Oort, B. E. H. et al. Circadian organization in reindeer. Nature 438, 1095–1096, https://doi.org/10.1038/4381095a (2005).
van Oort, B. E. H., Tyler, N. J. C., Gerkema, M. P., Folkow, L. & Stokkan, K. A. Where clocks are redundant: weak circadian mechanisms in reindeer living under polar photic conditions. Naturwissenschaften 94, 183–194, https://doi.org/10.1007/s00114-006-0174-2 (2007).
Kauranen, H. et al. Flies in the north: locomotor behavior and clock neuron organization of Drosophila montana. J. Biol. Rhythms 27, 377–387, https://doi.org/10.1177/0748730412455916 (2012).
Menegazzi, P. et al. Adaptation of circadian neuronal network to photoperiod in high-latitude european Drosophilids. Curr. Biol. 27, 833–839, https://doi.org/10.1016/j.cub.2017.01.036 (2017).
Vaze, K. M. & Helfrich‐Förster, C. Drosophila ezoana uses an hour‐glass or highly damped circadian clock for measuring night length and inducing diapause. Physiol. Entomol. 41, 378–389, https://doi.org/10.1111/phen.12165 (2016).
Saunders, D. S., Henrich, V. C. & Gilbert, L. I. Induction of diapause in Drosophila melanogaster: photoperiodic regulation and the impact of arrhythmic clock mutations on time measurement. Proc. Natl. Acad. Sci. USA 86, 3748–3752 (1989).
Acknowledgements
This research was supported by funds from the German Research Foundation CRC 1047 projects A1 and C3.
Author information
Authors and Affiliations
Contributions
K.B. and J.J. designed the study, collected and analysed data (K.B.: locomotor activity, J.J.: metabolic activity) and wrote the manuscript. A.A.S. contributed to study design and data collection (locomotor activity). J.K. and C.H.-F. conceived the project, contributed funding, guided research and revised the manuscript.
Corresponding authors
Ethics declarations
Competing Interests
The authors declare that they have no competing interests.
Additional information
Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Beer, K., Joschinski, J., Arrazola Sastre, A. et al. A damping circadian clock drives weak oscillations in metabolism and locomotor activity of aphids (Acyrthosiphon pisum). Sci Rep 7, 14906 (2017). https://doi.org/10.1038/s41598-017-15014-3
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-017-15014-3
This article is cited by
-
Drosophila ezoana uses morning and evening oscillators to adjust its rhythmic activity to different daylengths but only the morning oscillator to measure night length for photoperiodic responses
Journal of Comparative Physiology A (2023)
-
The circadian and photoperiodic clock of the pea aphid
Journal of Comparative Physiology A (2023)
-
Photoperiodic time measurement, photoreception, and circadian clocks in insect photoperiodism
Applied Entomology and Zoology (2022)
-
Antixenosis in Glycine max (L.) Merr against Acyrthosiphon pisum (Harris)
Scientific Reports (2021)
-
Variation in susceptibility of rapeseed cultivars to the peach potato aphid
Journal of Pest Science (2021)
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.