Endogenous timing mechanism controlling the circannual pupation rhythm of the varied carpet beetle Anthrenus verbasci

This paper describes the detailed characteristics of the circannual pupation rhythm in Anthrenus verbasci determined by laboratory experiments under various photoperiods and temperatures. The frequency distribution of larval duration showed a periodic pattern over 2-3 years and the period was 37-40 weeks under a constant short-day photoperiod (light:dark 12:12) at 20 degrees C. This rhythm showed temperature compensation to some extent under a short-day photoperiod between 17.5 degrees C and 27.5 degrees C. Under alternations of a long-day (light:dark 16:8) and a short-day photoperiod, pupation occurred 21-24.5 weeks after transfer from a long-day to a short-day photoperiod. Therefore, we concluded that the timing of pupation in A. verbasci is controlled by a circannual rhythm and its zeitgeber is a change in photoperiod. Furthermore, when larvae were transferred from a long-day to a short-day photoperiod at various ages, the larval duration after the photoperiodic transfer depended on the time of the transfer. This difference can be explained by phase-dependent phase shifts in the circannual rhythm.     

Circannual pupation rhythm in the varied carpet beetle Anthrenus verbasci under different nutrient conditions

Anthrenus verbasci pupates in spring and the timing of pupation is controlled by a circannual rhythm. Although A. verbasci is considered to be a univoltine species in Japan, it is assumed that larval development in its natural habitats, including bird nests, varies with nutrient availability, and that the life cycle often takes two or more years to complete. In the present study, larval development and pupation times were compared under constant and outdoor conditions in larvae provided a diet of either high‐nutrient bonito powder or low‐nutrient pigeon feathers. Although a circannual pupation rhythm was observed irrespective of the diet used, larval development was slower on feathers than on bonito powder. The pupation times on feathers varied over three years or more under both constant and outdoor conditions. Under outdoor conditions, larvae grown on feathers needed three years to approach the weight gained within a year by larvae grown on bonito powder. It is considered that life cycle length in A. verbasci is often two years or more in nutritionally unstable natural habitats, and that this species has probably evolved a circannual rhythm as a seasonal adaptation to nutrient‐poor environments.     

Hormonal regulation of pupation in the codling moth, Laspeyresia pomonella

ABSTRACT. According to the different reactions to the juvenoid Altosid®, the last larval instar (L₅) of Laspeyresia pomonella (L.) (Tortricidae) reared under 'long day' conditions (constant light) was subdivided into three sensitive phases: an additional larval instar, a larval–pupal intermediate, or a pupa. Under short day conditions, the prothoracotropic effect of juvenile hormone (JH) in L₅, which have a continuous high titre of JH during the whole instar, indicated that it is not a particular titre of JH but a rise in the titre that can induce the production of moulting hormone. Neck-ligation experiments showed that JH acts not directly on the prothoracic glands but via the head, probably via the neurosecretory system. The meaning of the JH-peak in mature L₅ reared under long days was determined either by injections with the anti-JH, precocene II, in combination with applications of Altosid, or by forcing precocene-treated larvae to a precocious moult by injecting them with ecdysterone. Precocene delayed, and JH accelerated pupation if administered 4.5 days after the L₅ -moult. JH was also found to stimulate the growth and differentiation of the imaginal discs. Moulting hormone in long-days reared insects was detected one day after the larvae had spun their cocoon, with a maximum on the second day after spinning. The hormone was also present in freshly moulted pupae. Neck-ligation of mature larvae indicated that the delay between activation of the prothoracic glands and the production of an effective amount of moulting hormone is less than one day.     

Drosophila salivary gland proteins and pupation

Pulse-labeling experiments of salivary glands from the prepupal stages of development showed selectively high rates of synthesis of a set of low molecular weight proteins (6K–12K). These proteins are stably maintained in the salivary glands during prepupal development and are subsequently transported to the pupation fluid (found between the pupal case and the prepupal cuticle) when pupation occurs. These small polypeptides are very basic with the major components having isoelectric points of 8.6–8.7 and the minor components having isoelectric points of 9.1–9.5. This study shows the continuing function of the salivary glands—specifically, the synthesis and secretion of a set of proteins with a putative role in pupation.     

Selection for pupation height in Drosophila melanogaster

Divergent directional selection for high and low pupation height was practiced in D. melanogaster. A quick response was observed in the two directions of selection. This is the first time selection for low pupation sites was successful. Realized heritabilities were 18% and 13% for the high and low lines. Reciprocal crosses between divergent lines showed little or no dominance for low pupation sites. The need for a strict control of environmental factors when measuring pupation height is emphasized.     

Diapause, pupation sites and parasitism of the horn fly, Haematobia irritans, in south-eastern Brazil

In order to verify the occurrence of diapause, preference for pupation sites and hymenopteran parasitism, the pupae of the horn fly, Haematobia irritans (Diptera: Muscidae), were collected from undisturbed cattle dung pats in pastures, and adults of the fly were sampled from cattle in São Paulo State, south-eastern Brazil, from April 1993 to July 1994. Diapause was verified in 7.7% of pupae sampled from pastures in June and July of 1993 and in 9.9% of those sampled in May, June and July of 1994 (overall rate of 9.1%). Approximately 8.3% of the pupae were parasitized by microhymenopterans, mostly Spalangia nigroaenea and S.cameroni (Hymenoptera: Pteromalidae). Horn fly pupae were found almost exclusively inside the pat or in the soil immediately beneath and adjacent to it, and very few were collected elsewhere. Pupa mortality was 54.4% and did not change significantly during the year, but mortality was greater among pupae collected in pastures when compared to those obtained from experimental pats, lacking natural enemies.     

稻纵卷叶螟卷叶有虫率与化蛹率关系的研究

探索利用稻纵卷叶螟 Cnaphalocrocis medinalis（Guenée）卷叶有虫率估测化蛹率的方法和途径。本文基于稻纵卷叶螟化蛹进度的田间调查数据,用化蛹率（y）和卷叶有虫率（x）分别拟合直线函数、一元二次函数、一元三次函数、对数函数、指数函数和幂函数6种不同模型。结果表明,以一元三次函数方法估计精度最高,误差最小,应用效果最好,并根据最优数学模型建立化蛹率（y）与卷叶有虫率（x）的关系速查表。生产中可以应用拟合的 最优数学模型对田间稻纵卷叶螟化蛹进度进行监测。     

Implications of Chaoborus pupation and ecdysis in cold water

1. Cold water acted differently to delay and lengthen the pupation period for the larvae of two species of the zooplankton predator Chaoborus (Diptera: Chaoboridae). During Chaoborus pupation, the zooplankton community is released from predation, while the dark-coloured Chaoborus pupae are more susceptible to their own predators.
2. Fourth instar larvae of Chaoborus americanus and C. trivittatus , collected from an oligotrophic lake, were reared individually at 5 °C in the dark. Chaoborus americanus was also reared at 9 and 12 °C under spring photoperiod conditions (L : D, 16 : 8 h). Individuals were observed through pupation to emergence (ecdysis) or death.
3.  Chaoborus americanus pupated at 5, 9 and 12 °C with substantial emergence only at 12 °C. In comparison, C. trivittatus emerged at 5 °C. Light was not a necessary cue for pupation and ecdysis, contrary to previous reports. Cold water delayed the onset and lengthened and increased the variability of the duration of pupation.
4. In Shirley Lake, C. americanus pupated in late June–early July while C. trivittatus pupated first in April and again in June–July.
5.  Chaoborus americanus pupae needed a temperature cue to complete ecdysis. The ecdysis temperature threshold helps to explain the difference in pupation timing, and the geographical distribution, of C. americanus and its relatively inflexible life history contrasted with C. trivittatus . Delayed predator pupation in years with low spring temperature can affect the community dynamics of the prey.     

Asynchronous pupation of univoltine insects as evolutionarily stable phenology

Evolutionarily stable seasonal timing of larval feeding stages is studied theoretically for univoltine insects. In the evolutionarily stable (or ESS) population, each individual maximizes its own lifetime reproductive success by choosing the hatching and pupation dates, given the resource availability curve with a peak in the middle of a year, a higher daily mortality in the feeding stages, and the growth rate decreasing with the larval biomass in the population. If growth rate is proportional to the body size, the population at the ESS is composed of a mixture of phenotypes differing in hatching and pupation, but pupation interval over which some popation occur every day is much longer than hatching interval. If growth rate increases with the body size at a speed slower than linearly, large sized larvae should pupate earlier than small ones.     

纳米银对果蝇化蛹、羽化、寿命及细胞凋亡和蛋白表达的影响

纳米银因具有强有效的抗菌作用而被广泛应用于医药领域,然而它存在潜在的生物毒性.本研究选取经典的模式生物黑腹果蝇,探究纳米银对生物体的毒性作用机理.测定不同浓度纳米银处理下的Oregon R、w1118、MTF突变体等品系的化蛹率、羽化时间、羽化率及寿命;用rpr-lacZ品系的lacZ活性测定不同纳米银浓度处理下翅成虫盘的细胞凋亡情况; 通过SDS-PAGE研究不同浓度纳米银浓度处理下MTF突变体中肠蛋白的表达差异,并利用质谱分析差异蛋白的氨基酸序列.结果显示: 纳米银处理浓度升高至200 μg·mL^-1及以上时,MTF突变体化蛹率和羽化率显著降低; 纳米银处理浓度升高至800 μg·mL^-1时,Oregon R和w1118化蛹率和羽化率显著降低,而化蛹时间和羽化时间与纳米银处理浓度无显著关系.不同浓度纳米银处理对Oregon R和w1118的寿命无影响,而200 μg·mL^-1纳米银显著降低MTF突变体平均寿命.随纳米银处理浓度升高,细胞凋亡也逐渐增多.SDS-PAGE及质谱分析表明,随纳米银浓度上升,质子泵ATP激酶、热激蛋白、糖代谢相关酶系等蛋白的表达量上升.本研究表明,高浓度的纳米银会促进细胞凋亡致使部分蛋白表达量发生改变,从而降低果蝇存活率,为后续进一步了解其毒性作用机理提供理论依据.     

Larval pupation site preference in a few species of Drosophila

Larval pupation site preference (PSP) is an important event in preadult development. The PSP was studied on the basis of the number of larvae pupated at different sites in the cultures. The results revealed that the larval PSP in different species of Drosophila varies significantly at different sites. The sympatric species also differ in their PSP and the pupation behaviour does not correspond with the taxonomic relationship between the species.     

Granulovirus prevents pupation and retards development of Adoxophyes honmai larvae

Abstract Larvae of Adoxophyes honmai (Lepidoptera: Tortricidae) infected with granulovirus (AdhoGV) do not pupate; instead, they undergo prolonged larval development and die during the final stadium. Non-infected larvae, however, pupate after five larval stadia. Insect metamorphosis is regulated by fluctuations of ecdysteroid and Juvenile Hormone (JH). JH esterase activity and titres of ecdysteroid must be measured to understand fully the interaction of an insect virus and its host. JH esterase activity is consistently low in AdhoGV-infected larvae, which suggests that JH in AdhoGV-infected larvae is not degraded during the final stadium. The ecdysteroid titre in non-infected larvae showed a large peak in the final stadium before pupation, whereas that in AdhoGV-infected larvae increased from day 2 to day 5 in the final stadium, and then remained at a high level until death. Furthermore, an ecdysteroid UDP-glucosyltransferase (EGT) assay showed that this activity occurs in haemolymph from AdhoGV-infected larvae, but not in haemolymph of non-infected larvae. PCR and sequencing analysis revealed that the AdhoGV genome contains an egt gene, which encodes a protein of 445 amino acids, located approximately 1 kbp upstream from the granulin gene. These results suggest that AdhoGV-infected larvae are prevented from pupating because JHE activity is suppressed and EGT expression inactivates ecdysteroid in the haemolymph.     

The earliest evidence of holometabolan insect pupation in conifer wood

Background

The pre-Jurassic record of terrestrial wood borings is poorly resolved, despite body fossil evidence of insect diversification among xylophilic clades starting in the late Paleozoic. Detailed analysis of borings in petrified wood provides direct evidence of wood utilization by invertebrate animals, which typically comprises feeding behaviors.

Methodology/Principal Findings

We describe a U-shaped boring in petrified wood from the Late Triassic Chinle Formation of southern Utah that demonstrates a strong linkage between insect ontogeny and conifer wood resources. Xylokrypta durossi new ichnogenus and ichnospecies is a large excavation in wood that is backfilled with partially digested xylem, creating a secluded chamber. The tracemaker exited the chamber by way of a small vertical shaft. This sequence of behaviors is most consistent with the entrance of a larva followed by pupal quiescence and adult emergence — hallmarks of holometabolous insect ontogeny. Among the known body fossil record of Triassic insects, cupedid beetles (Coleoptera: Archostemata) are deemed the most plausible tracemakers of Xylokrypta, based on their body size and modern xylobiotic lifestyle.

Conclusions/Significance

This oldest record of pupation in fossil wood provides an alternative interpretation to borings once regarded as evidence for Triassic bees. Instead Xylokrypta suggests that early archostematan beetles were leaders in exploiting wood substrates well before modern clades of xylophages arose in the late Mesozoic.     

Influence of parasitism and soil compaction on pupation of the green bottle fly,Lucilia sericata

The influence of parasitoids and soil compaction on pupation behavior of blow flies was examined in a host–parasitoid system involving Lucilia sericata (Meigen) (Diptera: Calliphoridae) and Nasonia vitripennis (Walker) (Hymenoptera: Pteromalidae). Larvae of L. sericata were introduced to containers with soil of different compaction levels, with or without parasitoids. Although females of N. vitripennis did not significantly affect the pupation depth of L. sericata, they increased the rate of pupal development by 15.0–23.7 h at 28.4 ± 1.2 °C, and increased the clumping of puparia. Pupation depth of L. sericata was negatively related to soil compaction; mean depth of pupation was 4.4 cm in uncompacted soil and 0.5 cm in high‐compaction soil. In high‐compaction soil, pupal development increased by 10.5–18.8 h at 25.2 ± 0.3 °C, and puparia were clumped. These results provide a framework for locating puparia in forensic investigations and releasing appropriate parasitoids for biological control of blow flies.     

Pupal colour dimorphism in California Battus philenor: pupation sites, environmental control, and diapause linkage

ABSTRACT.

• 1 Natural pupation sites and corresponding pupal colour (green or brown) were determined for samples of Battus philenor (L.) from two Californian populations.
• 2 Larvae pupate off the ground on trees, shrubs and man-made objects.
• 3 The vertical distribution of pupation sites and relative frequencies of pupae formed on narrow twigs and broad substrates show interpopulation variability, and seem to be determined by habitat-specific and possibly behavioural differences among populations.
• 4 The percentage of‘mismatched’pupae in green leafy environments (brown) is greater than that on wide substrates (green). Heterogeneity in samples of the latter suggest strong but sporadic predation pressure on non-cryptic pupae in exposed areas.
• 5 Green and brown substrates generally promoted formation of cryptic green and brown pupae although rearing conditions modified pupal colour response to substrate colour and larval pupation site choice.
• 6 Warm temperatures and long days increased the production of brown pupae. Short photoperiods increased the tendency of larvae to pupate on narrow twig-like substrates and to form green pupae.
• 7 Green pupae show less tendency to diapause than brown pupae. The difference between percentage diapause in the two colour forms increases under conditions favouring progressively more continuous development.