'Bistability' experiments and photoperiodic morph determination in the aphid Aphis fabae

Abstract. Newly born larvae (presumptive gynoparae) of the aphid Aphis fabae were exposed to 'symmetrical skeleton' photoperiods, consisting of two equal pulses of light per 24 h. The general form of the photoperiods tested was LDLD 1:10:1:12 h. This regime is open to two 'interpretations', LDLD 1:10:1:12 h (PP_s12) and LDLD 1:12:1:10 h (PP_s14). As both light pulses are close to 12 h apart, it is expected that the interpretations result in two distinct steady state phase relationships, i.e. this regime would show bistability. If this is true and both interpretations could be adopted, PP_s12 is expected to result in a low and PP_s14 in a high percentage of 'apterized' insects.
Experiments undertaken with the aphid showed that bistability did not occur either at 15C or 20C, and the results could be entirely explained on the basis of an 'instantly' damping circadian oscillator clock.     

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.     

Net biome production of the Amazon Basin in the 21st century

Global change includes multiple stressors to natural ecosystems ranging from direct climate and land‐use impacts to indirect degradation processes resulting from fire. Humid tropical forests are vulnerable to projected climate change and possible synergistic interactions with deforestation and fire, which may initiate a positive feedback to rising atmospheric CO₂. Here, we present results from a multifactorial impact analysis that combined an ensemble of climate change models with feedbacks from deforestation and accidental fires to quantify changes in Amazon Basin carbon cycling. Using the LPJmL Dynamic Global Vegetation Model, we modelled spatio‐temporal changes in net biome production (NBP); the difference between carbon fluxes from fire, deforestation, soil respiration and net primary production. By 2050, deforestation and fire (with no CO₂ increase or climate change) resulted in carbon losses of 7.4–20.3 Pg C with the range of uncertainty depending on socio‐economic storyline. During the same time period, interactions between climate and land use either compensated for carbon losses due to wetter climate and CO₂ fertilization or exacerbated carbon losses from drought‐induced forest mortality (?20.1 to +4.3 Pg C). By the end of the 21st century, depending on climate projection and the rate of deforestation (including its interaction with fire), carbon stocks either increased (+12.6 Pg C) or decreased (?40.6 Pg C). The synergistic effect of deforestation and fire with climate change contributed up to 26–36 Pg C of the overall decrease in carbon stocks. Agreement between climate projections (n=9), not accounting for deforestation and fire, in 2050 and 2098 was relatively low for the directional change in basin‐wide NBP (19–37%) and aboveground live biomass (13–24%). The largest uncertainty resulted from climate projections, followed by implementation of ecosystem dynamics and deforestation. Our analysis partitions the drivers of tropical ecosystem change and is relevant for guiding mitigation and adaptation policy related to global change.     

Sexual selection is stabilizing selection in pupfish [Cyprinodon pecosensis)

One of the predictions of the 'good genes' model of sexual selection is that reproductively successful males with well-developed indicator traits should show smaller variances for non-indicator traits, that are not directly associated with mating success, when compared to non-breeding males and females. Thus sexual selection should reinforce stabilizing natural selection in reducing the variance in quantitative traits. This prediction is tested by analysing variation in eight morphological traits of breeding males, non-breeding males, and females of pupfish (Cyprinodon pecosensis). Breeding males tended to be less variable than non-breeding males for all principal component factors, and for all morphological traits except for depth, although these differences were statistically significant only for PC2, and PC5 and for pelvic fin length, number of pelvic fin rays and number of preopercular and preorbital pores. Similarly, breeding males tended to be less variable than females for all principal component factors and for all morphological traits except for number of preopercular pores. These differences were statistically significant for PC2, and for depth, pelvic fin length, number of preorbital pores and pectoral fin rays. The overall pattern of reduced variability in independent traits of breeding males revealed by principal component analysis is very consistent and highly significant (P<10⁵). These results support the prediction of the 'good genes' model and show that reproductively active males are subject to more severe stabilizing selection for several quantitative traits than non-breeding males and females. Thus sexual selection, through male-male competition, female choice, or an interaction of both selective processes, results in stabilizing selection on quantitative morphological traits.     

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.     

Untersuchung zum Einfluß des Erkundungs- und Spielverhaltens auf das Lernen bei Iltisfrettchen (Mustela putorius X M. furo)

This paper investigates the dependence of learning performance on previous exploration and playing with objects. The subjects are polecats (Mustela putorius X M. furo). Behaviour of social animals, who are offered changing tube systems in certain periods, is described and analysed. A maze-test shows that subjects with tube training are superior to subjects without tube training as regards acquisition and reversal learning. The learning performance in pattern recognition tests is the same in all tests with the different groups, however.     

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.