Termination of diapause in the Cinnabar moth (Tyria jacobaeae) by chilling

The effect of chilling time on the termination of pupal diapause was studied in the Cinnabar moth, Tyria jacobaeae L., Lepidoptera: Arctiidae. Chilling followed by a temperature of 20°C was effective in terminating diapause. Chilling for 120 days immediately after pupation yielded the highest percentage emergence and resulted in the shortest total pupal development time (162 days). A more natural treatment, a warm period before cold treatment, did not result in a higher percentage of emergence or in a shorter total pupal development time.During hibernation this species experiences two successive processes: diapause development during the first three to four months of cold, followed by a period of quiescence. Application of high temperatures in this latter period immediately starts morphogenesis. The impact of a relative humidity of 70% during the pupal stage for complete wing unfolding is demonstrated. The underlying mechanism of diapause is discussed.

---

Résumé L'effet sur la levée de la diapause de différents régimes de température infligés aux chrysalides est étudié chez Tyria jacobaeae L. (Lepidoptera: Arctiidae). Une mise au froid suivie de hautes températures lève efficacement la diapause. Un refroidissement pendant 120 jours immédiatement après la nymphose entraîne le plus grand pourcentage d'éclosions et la durée totale du développement des chrysalides la plus courte (162.3 j). Un traitement plus naturel, une période chaude avant la période froide, n'entraîne pas un plus grand pourcentage d'éclosions ni une durée plus courte de développement.Il est proposé que durant l'hibernation cette espèce passe par deux processus successifs: un diapause durant les premiers trois ou quatre mois de froid, suivie d'une période de quiescence. Le transfert à des hautes températures pendant cette derpériode déclanche immédiatement la morphogénèse. L'influence d'un taux élevé d'humidité relative durant le stade chrysalide sur le déploiement complet des ailes est démontré. Le méchanisme de diapause sous-jacent est discuté.

     

The population ecology of the Cinnabar Moth,Tyria jacobaeae L. (Lepidoptera,Arctiidae)

Summary This paper describes the results of a study of the factors determining the abundance and distribution of the Cinnabar Moth in Britain. The main part of the study was on a population of the moth at Weeting Heath in Norfolk. This is an area of sandy heath which is heavily overgrazed by rabbits. Here the moth fluctuates violently in number and periodically it completely defoliates its food plant (ragwort, Senecio jacobaea L.) over large areas. This happened in 1960, 1961, 1967, and 1968.Since 1966, the numbers of the moth have been studied in detail and Life Tables are presented for five years.Adult fecundity varies considerably between years. This is due mainly to fluctuations in adult size resulting from changes in larval density. By comparison adult mortality and dispersal have little effect on fecundity; although there is some evidence to suggest that dispersal is density dependent. Because the number of eggs laid in one generation depends on the size of the previous generation, fecundity tends to be acting as a delayed density dependent factor.Mortality is low during the egg stage, but is high amongst young larvae, due mainly to arthropod predation. As the caterpillars grow they become immune from this predation. They are distasteful to vertebrate predators.A larval parasite, Apanteles popularis, kills many of the fully grown larvae. The highest rates of parasitism have coincided with the lowest densities of the moth, however, so that over the five years it has acted as an inverse density dependent factor.In 1967, the population became so large that the ragwort was completely defoliated, and about 20% of the caterpillars died from starvation. In the following year the population was still large and the ragwort plants were small, owing to the effects of defoliation in the previous year. Food ran out early in the season and about 50% of the larvae starved. Because of the overriding effect of starvation, total larval mortality tends to be density dependent.Mortality is high at, or immediately after, pupation and this is thought to be due primarily to predation by moles (Talpa europaea). Pupal mortality does not appear to be density dependent.The upward growth of the population is limited by food supply. Starvation led to a population crash, so that in 1969 only 62 eggs/150 m² were laid compared with 17110 and 16493 in the previous two years. The rate of recovery of the population after this crash was dependent upon the rapid recovery of the ragwort plants. Owing to the wet summer in 1968, plant numbers actually increased after defoliation, due to regeneration from root buds. This was in spite of the fact that no seed was produced in the area in either 1967 or 1968.The only factor which appears to buffer the population against extinction in years when food runs out early in the season, is the heterogeneity within the moth and ragwort populations. The earliest individuals manage to obtain sufficient food in those patches of ragwort which survive longest.Large fluctuations in number only occur in some localities. Other populations of the moth persist at low density and never eat out their food supply. Some data are presented from such a population at Monks Wood. This site is on a heavy clay soil, rabbit grazing is less marked than at Weeting, and ragwort occurs only at a low density. The lusher vegetation supports a very large population of arthropod predators and these take a higher percentage of the young caterpillars than was found at Weeting. Pupal survival is also low due probably to waterlogging of the soil. Pupae can withstand considerable desiccation, but excessive moisture soon leads to their death.The distribution of the moth in Britain and its use for the biological control of ragwort are discussed.     

Facultative defences and specialist herbivores? Cinnabar moth (Tyria jacobaeae) on the re growth foliage of ragwort (Senecio jacobaea)

Abstract. 1. Ovipositing females of cinnabar moth lay just as many eggs on regrowth foliage as on normal rosette leaves of ragwort.
2. Larvae reared on regrowth tissues achieve the same weight at pupation as insects fed on primary leaves and capitula. Diet affected neither survival rate nor development time.
3. Larvae from eggs laid on normal foliage achieve lower pupal weights when fed regrowth tissues, and larvae from eggs laid on regrowth leaves perform less well on a diet of normal foliage.
4. The complex of changes associated with re growth following defoliation does not appear to reduce the fitness of this specialist herbivore, nor does it reduce the likelihood that the plant will be attacked by ovipositing adult moths.
5. A facultative response which consisted of an increase in 'qualitative defences' is unlikely to be effective against adapted herbivores.     

Increase in respiratory rate during feeding in larvae of the cinnabar moth Tyria jacobaeae

ABSTRACT. This study tested the effect of diet and phase of the feeding cycle on oxygen consumption by fifth-instar larvae of the cinnabar moth Tyria jacobaeae (L.) (Lepidoptera: Arctiidae). There was no significant variation in respiratory rates among larvae fed different diets, which were floral parts, upper, middle and lower leaves of the host plant tansy ragwort, Senecio jacobaea. The respiratory rates ( x ± 95% Cl μlO₂h^-1) of feeding larvae (279.5 ± 30.9) were higher than those of larvae at rest (179.7 ± 12.2), but were not significantly different from those of larvae in the post-ingestive phase (272.8 ± 35.8).
The respiratory rates of feeding larvae increased linearly with the ingestion rate, such that an additional 21.1 μl O₂ were consumed for every mg dry mass of plant material eaten per hour.     

The influence of nutritional and genetic factors on larval performance of the cinnabar moth, Tyria jacobaeae

In a laboratory experiment using full-sibs, 60% of the variation in pupal weight of the monophage Tyria jacobaeae L. (Lepidoptera, Arctiidae) could be explained by variation in the nitrogen concentration of the food plant, Senecio jacobaea L. and only 4% by variation in sugar concentration. Larval weight and growth rates of young and old larvae were also positively correlated with nitrogen and sugar concentration. Developmental time was negatively correlated with nitrogen concentration. In a second experiment full-sib families differed significantly in larval weight at day 7, mortality, growth rate and developmental time. Pupal weight did not differ significantly among families, but was positively correlated with nitrogen concentration of Senecio. Larval performance was not significantly influenced by concentrations of sugars or alkaloids. We conclude that larval performance of Tyria during most of the larval period is mainly determined by genetic factors, but pupal weights are primarily determined by nitrogen concentration of the food plant.     

Pleistophora finisterrensis n. sp., a microsporidian parasite of blue whiting Micromesistius poutassou

Pleistophora finisterrensis n. sp. is a microsporidian parasite of the hypoaxial musculature of the blue whiting Micromesistius poutassou (Risso). Foci of infection are between 3 and 6 mm in length and have no evident effects on adjacent muscle fibres. We found only a single type of spore (uninucleate, with mean dimensions of 4×2 µm in fresh preparations), contained within sporophorous vesicles (mean diameter 19 µm in fresh preparations; 150–250 spores per vesicle). All of the development stages of this microsporidian are monokaryotic. The meronts are initially uninucleate and bounded by a plasmalemma. Towards the end of merogony, meronts are multinucleate plasmodia with a well-defined surface coat. Sporogony is polysporous, with multinucleate sporonts, which likewise have a well-defined surface coat (about 130 nm thick), dividing by plasmotomy to give rise to uninucleate sporoblasts. The polar tube is isofilar and consists of 8–9 turns in the posterior half of spore. The polaroplast is made up of an anterior lamellar part and a posterior vesicular part.     

A microsporidium,Nosema pilicornis sp. n., of the purslane sawfly,Schizocerella pilicornis

A new microsporidian species, Nosema pilicornis, which infects the purslane sawfly, Schizocerella pilicornis, is described. This microsporidium infects most body tissues of the host. N. pilicornis was compared to other microsporidian species infecting Hymenoptera and to a group of similar microsporidia infecting Lepidoptera. N. pilicornis could be distinguished from all other microsporidian species on the basis of host range and ultrastructural characteristics of the spore. Spores were oval, containing 11 to 12 polar filament coils, and the polar filament had an angle of tilt of about 80°. N. pilicornis infected lepidopteran larvae, but only when heavy spore dosages were fed to early larval instars. S. pilicornis is a good but sporadic biological control agent of common purslane, Portulaca oleracea, a pernicious weed of vegetable, ornamental, and orchard crops. N. pilicornis, which is transovarially transmitted and causes high mortality in infected larvae, affects the performance of S. pilicornis as a biological control agent.     

Nosema parkeri sp. n., a microsporidan from the argasid tick, Ornithodoros parkeri Cooley.

Nosema parkeri sp. n. is described from nymphs and adults of the argasid tick, Ornithodoros parkeri Cooley, from a laboratory colony. Schizogonic and sporogonic stages are described from various tick tissues. Spores are binucleate, measuring 3.2 (3-4) x 1.9 (1.8-2.5) micronm. Transmission is transovarial and transstadial. The parasite does not appear to affect adversely the development or reproduction of the tick. Dermacentor andersoni Stiles was experimentally infected. Attempts to infect Swiss mice by tick feeding or by injection of infected tick suspensions were unsuccessful. The microsporidan differs in structure from Encephalitozoon ixodis Weiser) and Nosema slovaca Weiser & Rehácek, the only other microsporidans known from ticks.     

Nosema parkeri sp. n., a Microsporidan from the Argasid Tick, Ornithodoros parkeri Cooley

SYNOPSIS. Nosema parkeri sp. n. is described from nymphs and adults of the argasid tick, Ornithodoros parkeri Cooley, from a laboratory colony. Schizogonic and sporogonic stages are described from various tick tissues. Spores are binucleate, measuring 3.2 (3–4) × 1.9 (1.8–2.5) μm. Transmission is transovarial and transstadial. The parasite does not appear to affect adversely the development or reproduction of the tick. Dermacentor andersoni Stiles was experimentally infected. Attempts to infect Swiss mice by tick feeding or by injection of infected tick suspensions were unsuccessful. The microsporidan differs in structure from Encephalitozoon ixodis Weiser) and Nosema slovaca Weiser & Reháček, the only other microsporidans known from ticks.     

Inter- and intra- species differences in plants as hosts to shape Tyria jacobaeae

The effects of sublethal doses of deltamethrin and propoxur, applied topically at LD10, LD30 and LD50 on German cockroaches, were studied by reciprocal crossing. Male and female longevities decreased curvilinearly with increasing sublethal doses of deltamethrin, and decreased linearly with increasing sublethal doses of propoxur. Fecundity of females treated with deltamethrin and propoxur was reduced with increasing sublethal doses of both insecticides. Oothecal production, oothecal hatchability and nymphal production also declined with increasing doses of deltamethrin and propoxur. Preoviposition and incubation periods were not affected by sublethal doses of deltamethrin and propoxur, although some significant differences were observed at certain oothecal numbers. Two-way analysis of variance indicated that only treated females showed an effect on oothecal production while oothecal hatch and nymphal production were governed by both treated females and males. Insecticide susceptibility tests on the progeny of parents treated with sublethal doses demonstrated that these doses did not increase insecticidal tolerance in the F1 generation.     

Erhardorina n. g., Ascogregarina polynesiensis n. sp., Eimeria golemanskii n. sp., Isospora tamariscini n. sp., Gregarina kazumii n. nom., new combinations and emendations in the names of apicomplexan protozoa

On the basis of a review of the approximately 4300 species of apicomplexan protozoa, the following new species, new names, new combinations, and emendations are given: NEW GENUS, Erhardovina; NEW SPECIES, Ascogregarina polynesiensis, Eimeria golemanskii, Isospora tamariscini; NEW NAME, Gregarina kazumii; NEW COMBINATIONS, Ascogregarina brachyceri (Purrini, 1980), Erhardovina euzeti (Lipa, 1981), E. scutovertexi (Erhardová, 1955), Haemorhormidium batrachi (Chaudhuri & Choudhury, 1983); EMENDATIONS, Selenidium francianum (Arvy, 1952) Tuzet & Ormières, 1965, Pyxinioides bolitoides D. P. Henry, 1938, P. japonicus H. Hoshide, 1951, P. kamenote H. Hoshide, 1951, P. kurofuji H. Hoshide, 1951, P. oshoroensis H. Hoshide, 1951, P. pugetensis D. P. Henry, 1938, Gregarina levinei Haldar & Sarkar, 1980, Retractocephalus halticae Haldar, Chakraborty & Kundu, 1982, Cnemidospora schizophylli Tuzet & Guerin, 1947, Grebneckiella indica (Merton, 1911) Watson, 1916, Quadruspinospora atractomorphae Haldar & Chakraborty, 1978, Haemogregarina acipenseri Nawrotzky, 1914, H. lobianci Yakimov & Kohl-Yakimov, 1912, H. yakimovikohlae Wladimiroff, 1910, Hepatozoon luehi (Sambon, 1909) Pessoa, Cavalheiro & de Souza, 1970, Eimeria beyerae Ovezmukhammedov, 1977, E. (?) gigantea (Labbé, 1896) Reichenow, 1921, E. (?) labbei Hardcastle, 1943, E. rufi Prasad, 1960, E. (?) scylii (Drago, 1902) Levine & Becker, 1933, Isospora corvi Ray, Shivnani, Oommen & Bhaskaran, 1952, I. melopsittaci Bhatia, Chauhan, Arora & Agrawal, 1973, I. seicerci Ray, Shivnani, Oommen & Bhaskaran, 1952, I. stomatici Chakravarty & Kar, 1944, I. triffitae Nukerbaeva & Svanbaev, 1973, Wenyonella mackinnonae Misra, 1947, Octosporella sanguinolentae Ovezmukhammedov, 1975, Lankesterella millani Alvarez Calvo, 1975, Sarcocystis woodhousei Dogel', 1916, Haemoproteus lari Yakunin, 1972, Babesia ninakohlyakimovae (Yakimoff & Shokhor, 1916), Theileria ninakohlyakimovae (Yakimov, 1916) Krylov, 1974, Haemohormidium batrachi (Chaudhuri & Choudhury, 1983).