Restriction fragment length polymorphisms of Anisakinae larvae

The analysis of restriction fragment length polymorphisms (RFLPs) was applied to distinguish several kinds of Anisakinae larvae, Anisakis larvae (type I) collected from two different paratenic hosts, Anisakis larvae (type II) and Contracaecum larvae. The patterns of the two different paratenic host-derived DNA of Anisakis larva (I) were exactly the same in hybridized fragments generated by six endonucleases. The quite different patterns in RFLPs of genomic DNA were observed among the Anisakis larva (I), Anisakis larva (II) and Contracaecum larvae. The results suggest that the RFLPs analysis may be useful for distinguishing Anisakinae larvae and clarifying the relationships between Anisakis larvae and their adult worms.     

Cocoon-spinning larvae of Oriental fruit moth and Indianmeal moth do not produce aggregation pheromone

1 Mature larvae of the Oriental fruit moth (OFM) Grapholita molesta (Lepidoptera: Tortricidae) and the Indianmeal moth (IMM) Plodia interpunctella (Lepidoptera: Pyralidae) leave their food source in search of suitable pupation sites in which to spin cocoons. These sites are typically well-concealed cracks and crevices within the environment. Such cocooning behaviour is also observed in larvae of the codling moth (CM) Cydia pomonella (Lepidoptera: Tortricidae), which aggregate prior to pupation in response to a pheromone blend produced by cocoon-spinning conspecific larvae.
2 In laboratory experiments, we tested whether cocoon-spinning OFM and IMM larvae produce aggregation pheromones and whether CM larvae are cross-attracted to closely-related OFM larvae.
3 Fifth-instar OFM and IMM larvae were not attracted to, or arrested by, cocoon-spinning conspecifics. Moreover, fifth-instar CM larvae were not cross-attracted to either cocoon-spinning OFM or IMM larvae.
4 Analyses of volatiles released from cocoon-spinning OFM and IMM larvae revealed that both OFM and IMM lack components that are present in the aggregation pheromone of CM larvae. This information may help explain why CM larvae are not cross-attracted to cocooning OFM or IMM larvae.     

Larval size relative to larval feeding, cannibalism of larvae, egg or adult female size and larval–adult setal patterns among 13 phytoseiid mite species

Phytoseiid mite larvae vary in size and feeding type. We compared larval size to feeding by larvae, cannibalism of larvae by adult females, egg and adult female size and the setae lengths of larvae and adults among 13 species. There was no relationship between size of larvae and either feeding by larvae or cannibalism of larvae by adult female mites. Correlations were highest between larval size as measured by idiosoma plus extended leg lengths and adult female size of idiosoma plus extended leg lengths (r²=0.746), while next highest was larval idiosoma length and adult female idiosoma length (r²=0.662) and then larval idiosoma length and egg length (r²=0.579). Based on idiosoma length, Phytoseiulus persimilis had the largest larvae (non-feeding) among species and Euseius finlandicus had the smallest larvae (obligatory feeding). However, based on idiosoma length plus extended leg length, obligatory feeding larvae (on pollen or mites) of E. finlandicus and Euseius hibisci were largest and facultative feeding larvae (on mites) of Neoseiulus californicus and obligatory feeding larvae (on mites) of Galendromus occidentalis were the smallest. Among species with non- or facultative feeding larvae, Amblyseius andersoni and Neoseiulus barkeri had larger larvae and Typhlodromus pyri and Neoseiulus fallacis had smaller larvae when leg lengths were included in larval size. Setae lengths of larvae versus adult females (after adjustment for body sizes) showed high correlation for j6 (r²=0.942) and s4 (r²=0.854), but low correlation for larval Z4 versus adult female Z4 (r²=0.084) or Z5 (r²=0.063). Overall, larval morphological traits were most closely correlated to traits of other life stages, although for setae there were some exceptions. Differences in the functions of setae j6, s4 and Z4 in the larva versus adult female are discussed.     

Setting tools for the early assessment of the quality of thawed Pacific oyster (Crassostrea gigas) D-larvae

Parameters used to assess the survival of larvae after cryopreservation generally misestimate the damages that prevent larval development. The objectives of the present study were to 1) define the reliability of the survival rate, assessed at 2 and 7 days post fertilization, to estimate Pacific oyster larval quality after thawing, and 2) select complementary tools allowing an early and reliable estimation of their quality. Oyster larvae were reared for 25 h after fertilization at 19 °C and cryopreserved at early D-stage. Then, thawed larvae were incubated in 2-L beakers. At 2 days post fertilization, the survival rate of thawed Pacific oyster larvae was lower than that of fresh larvae for only one experiment (Experiment 3) among the four identical experiments carried out in this work (Experiments 1-4). By contrast, the survival of thawed larvae, as assessed 7 days after fertilization, was lower than that of fresh larvae for the four experiments. These results confirm that the quality of thawed larvae is lower than that of fresh larvae and that the survival rate, estimated 2 days post fertilization, is not adapted to a reliable estimation of the subsequent development ability of thawed larvae. Then, complementary parameters were tested at 2 days: the movement characteristics (Experiments 1 and 2) and the morphologic features (Experiments 3 and 4) of thawed larvae. Compared to values observed on fresh larvae, the percentage of thawed motile larvae was different for only one experiment (Experiment 2) of the two. Compared to control, a reduced Average Path Velocity (VAP) of larvae (determined at the D-larval stage using a CASA-Computer Assisted Sperm Analysis-system) was observed after thawing for both experiments (Experiments 1 and 2), suggesting the ability of larval movement velocity to assess the decrease of the quality of thawed oyster larvae. Using an ASMA (Automated Sperm Morphology Analysis) device, a lower area of thawed larvae was observed, compared to control and for the two experiments (Experiments 3 and 4). By contrast, the Crofton perimeter of thawed larvae was lower than that of control larvae for only one experiment (Experiment 3) and no significant difference of circularity between fresh and thawed larvae was recorded for Experiments 3 and 4. In conclusion, changes in the movement velocity (assessed by CASA) and in the area (measured by ASMA) of D-larvae allow an early and reliable estimation of the quality of thawed Pacific oyster larvae.     

Helicoverpa armigera granulovirus interference with progression of H. zea nucleopolyhedrovirus disease in H. zea larvae

Capsular proteins from Helicoverpa armigera granulovirus (HaGV) have previously been shown to enhance H. armigera nucleopolyhedrovirus (HaSNPV) infection in H. armigera larvae. Yet, HaGV and HaS-NPV, as viable viruses, interfered with one another. In our study, we have examined the effects of co-infection of the slow-killing virus HaGV with the fast-killing virus Helicoverpa zea NPV (HzSNPV) on H. zea larvae. The mortality parameter measured was survival time. Virus stocks had 50% lethal concentrations of 3.2x10(-9) g HaGV-infected cadavers (GVC) (HaGV) and 32 occlusion bodies (HzSNPV) per cup. Average survival times were 16.8 and 5.5 days for larvae treated with HaGV and HzSNPV, respectively; death of HzSNPV-treated larvae was as early as 72 h posttreatment. In co-infection experiments in which larvae were treated concurrently with both viruses, the viruses competed in typical fashion for host resources. However, interference with disease progression in HzSNPV-fed larvae occurred even when HaGV was fed to larvae up to 36 h after the NPV, a time at which NPV infection should have been well established in host larvae. At death, co-infected larvae were observed microscopically to be filled with HaGV granules rather than HzSNPV polyhedra. The time study results imply that HaGV might be outcompeting HzSNPV by inhibiting its replication. We also observed that H. zea larvae treated with high dosages of HaGV (> or =3x10(-5) g GVC) were initially stunted but had survival times similar to those of larvae treated with lower dosages.     

Sublethal parameters in morphologically deformed Chironomus larvae: clues to understanding their bioindicator value

1. Parameters of condition between normal and deformed fourth instar larvae of Chironomus gr. thummi (Kieffer 1911) were compared in four populations: one reference (PE) and two metal-polluted sites (NP and SCH) in the River Dommel, and one site polluted by domestic sewage and copper in the River Ijse (NEI).
2. The site PE ranked lowest for metal body burdens, deformities, mortalities and emergence duration, while SCH and NEI ranked highest.
3. Deformed and non-deformed larvae most often did not differ in length and weight ( in situ end-points for growth); when differences occurred, deformed larvae tended to be smaller.
4. The energy content and dry weights in one population (NEI) were lower in normal larvae than in the weakly deformed ones. The percentage of ash-free dry weight was lower in deformed larvae of the polluted Dommel sites, compared to the normal ones.
5. The in vitro emergence rate (end-point for development of fourth instars) for the reference population PE, both in its own sediment and in artificial cellulose substrate, was better than for the other sites. In two populations (NEI, SCH) the development of deformed larvae in their own sediment was slower, with higher mortality, than for the normal larvae. In one population (NP), normal and deformed larvae survived and developed equally well. The emergence rates of the respective populations were similarly ranked when the larvae were raised in an artificial cellulose substrate.
6. Elution peaks of alleged metal-binding proteins were lower in deformed larvae from SCH and NEI, but higher in deformed larvae from NP, than in normal larvae.
7. A different development rate and mortality of deformed larvae in non-adapted populations and the possibility of metal adaptation, as in site NP, may modulate the final outcome of deformity frequencies, thus having an impact on the biomarker value of deformities in benthic midge larvae.     

微流水培养条件下斑鳜仔鱼的摄食与生长

在孵化环道连续微流水培养、水温(24±2)℃条件下,斑鳜(Siniperca scherzeri Steindachner)初孵仔鱼全长为(4.87±0.10)mm(n=50),卵黄囊体积为(1.461±0.172)mm3(n=50),油球直径为(0.47±0.04)mm(n=50).仔鱼孵出12h,胸鳍增大,具有一定阵发性水平游动能力,1日龄巡游模式建立;2日龄口膜消失,开始主动摄食,进入混合营养期,3 日龄外源性摄食关系完全建立.5日龄仔鱼的卵黄和油球全部消失.进入外源营养期;15日龄全长达到(13.72±0.76)mm(n=12).仔鱼发育过程中,其全长生长存在内源性营养阶段的较快速生长,混合营养阶段的慢速生长以及外源性营养阶段的快速生长三个生长期相,平均增长率为0.59 mm/d,对仔鱼全长TL(mm)与日龄D(d)进行同归,其生长模型为:TL=-0.0004D3+0.0283D2+0.2159D + 4.9335(R2=0.985,n=261).2-15 日龄,口宽与全长呈正比关系.仔鱼从初孵到PNR仅为5-6d,具有摄食能力的时间4d,仔鱼依赖外源性营养开始时间较早,对饥饿的耐受力较差.     

Effects of Microplitis croceipes Teratocytes on Host Haemolymph Protein Content and Fat Body Proliferation

Qualitative and quantitative changes in haemolymph proteins in Heliothis virescens were observed in larvae injected with either Microplitis croceipes teratocytes or teratocyte secreted proteins (TSP). Haemolymph protein titres in hosts receiving either 0.5 or 1 larval equivalent (LE) of teratocytes were similar to those of parasitized larvae, whereas a single injection of 4LE of TSP was required to induce a similar response. SDS-PAGE showed that the 82kDa monomer of riboflavin-binding protein and the 74/76kDa monomers of storage proteins were significantly reduced in parasitized larvae and in nonparasitized larvae treated with TSP. Concentrations of a 155kDa monomer (insectacyanin chromoprotein) also were reduced in parasitized larvae and those injected with either teratocytes or TSP. Two monomers (56 and 60kDa) were unique to parasitized larvae. Treated larvae required several days longer than controls to reach a comparable premetamorphic stage (burrowing-digging). Reductions in fat body proliferation similar to those seen in parasitized larvae were observed in larvae treated with either 1LE of teratocytes, or with 2 or 4LEs of TSP. Perivisceral fat body weights from larvae treated with either 0.25 or 0.5LE of teratocytes were significantly reduced, but less so than those which received 1LE. Thus, fat body proliferation in both teratocyte- and TSP-treated larvae was inhibited in a dose-dependent manner. Both light- and transmission electron microscopy observations revealed cytological differences in fat body tissues of larvae injected with either teratocytes or TSP from the condition observed in parasitized larvae and noninjected controls. Gross dissection of periviseral fat body from parasitized, teratocyte-injected and TSP-injected larvae showed tissue much less developed and differing considerably in appearance from controls. Observed differences included reduced size and/or number of lipid bodies and qualitative and quantitative changes in other cytoplasmic organelles.     

Asymmetric resource competition in a filter-feeding stream insect (Hydropsyche siltalai; Trichoptera)

SUMMARY. 1. Field experiments in a lake outlet stream were carried out on filter-feeding larvae of the caddisfly Hydropsyche siltalai Döhler, to assess whether microhabitat quality, establishment and growth rate is affected by position (upstream—downstream) within a dense aggregation of larvae.
2. Artificial substrates holding high-density aggregations of hydropsychid larvae were used. Marked III-instar H. siltalai larvae were implanted either in the upstream end or in the downstream end of an aggregation and recovered after 17 days.
3. Larvae recovered from the downstream end of an aggregation were smaller than those that had been implanted in the upstream end.
4. Fewer larvae had settled in the downstream end of aggregations compared to the exposed upstream part.
5. Naturally colonizing H. sitalai larvae were, in contrast to implanted larvae, more numerous behind aggregations. Small (first and second instar) Hydropsyche angustipennis (Curtis) and/or H. pellucidula (Curtis) larvae were more numerous in front of aggregations.
6. Current velocities, measured with a microcurrent velocity meter, and density of drifting prey, were significantly lower behind aggregations of hydropsychid larvae. Food availability decreased by about 50% behind aggregations.     

中红侧沟茧蜂寄生对寄主粘虫血淋巴糖类、脂类和蛋白质含量的影响

为揭示寄生蜂寄生对其寄主的生理调控机制, 室内对中红侧沟茧蜂Microplitis mediator寄生与未被寄生寄主粘虫Mythimna separata幼虫血淋巴中糖类、脂类和蛋白含量变化进行了测定。结果显示: 在滞育与非滞育条件下, 被寄生的粘虫血淋巴中糖原浓度均比未被寄生的粘虫高。滞育条件下寄生后12 d差异显著（P<0.05）, 被寄生粘虫糖原含量为7.93 μg/mL, 未被寄生粘虫糖原含量为4.70 μg/mL; 非滞育条件下寄生后6 d差异显著（P<0.05）, 被寄生粘虫糖原含量为14.35 μg/mL, 未被寄生粘虫糖原含量为5.47 μg/mL。海藻糖含量测定结果显示, 在滞育条件下寄生蜂对被寄生粘虫无明显影响, 而非滞育条件下影响效果差异显著（P<0.05）, 寄生后4 d被寄生粘虫海藻糖含量为46.82 μg/mL, 未被寄生粘虫含量为26.72 μg/mL。在滞育与非滞育两种条件下, 寄生与未被寄生寄主脂类和蛋白含量没有显著性差异。结果说明: 寄生蜂的存在使寄主血淋巴中的糖原含量增高; 非滞育条件是影响被寄生粘虫海藻糖含量变化主要因素; 粘虫对中红侧沟茧蜂的寄生表现相当强的适应性和忍受力。     

The possible contribution of pituitary hormones to the heterochronic development of gonads and external morphology in overwintered larvae of Hynobius retardatus.

In Hynobius retardatus, most larvae in regions of low elevation metamorphose by autumn of the same year. However, larvae of some populations found in cold, mountainous ponds cannot metamorphose within the year and become aged, overwintered larvae. Gonadal development in larvae under the age of 1 year (larvae developed from eggs spawned in the same year) and in aged, overwintered larvae (spawned and hatched in previous years) was examined at the same developmental stage (stage 63, full-grown larval stage). The number of germ cells and the cross-sectional areas of the gonads were much larger in 2-season-overwintered (third year) larvae than in larvae under the age of 1 year.To obtain reliable probes for investigating the possible contribution of TSH, FSH and LH to metamorphosis and gonadal development, cDNAs for Hynobius TSHbeta, FSHbeta and LHbeta genes were cloned. Their expressions were analyzed by means of semi-quantitative RT-PCR in larvae under the age of 1 year and in 2-season-overwintered larvae. No differences were observed in expression levels of either TSHbeta or LHbeta between larvae under the age of 1 year and the overwintered larvae. In contrast, expression of FSHbeta was much higher in the overwintered larvae than in larvae under the age of 1 year. These results suggest that gonadal development proceeds gradually with age even in the overwintered larvae, but that metamorphosis is retarded, probably due to the larvae's cold habitat. Heterochronic development of gonads and external morphology has been demonstrated in H. retardatus, suggesting a potency for neotenic reproduction in this species.     

A Tipula paludosa population with a high incidence of two pathogens

The incidence of lethal parasites in the larvae of a Tipula paludosa population was monitored for two seasons. The proportions of larvae infected with Tipula iridescent virus (TIV) and a tachinid insect were similar to those in previously studied populations, whereas the proportions of larvae infected with Tipula nuclear polyhedrosis virus (NPV) and a spore-forming bacterium (SFB) were higher. Conservative estimates of mortality due to these four agents were 10.7% in 1977–1978 and 7.7% in 1978–1979. The mean population density and the proportion of SFB-infected larvae were lower in 1978–1979 than in 1977–1978, while the proportion of NPV-infected larvae was higher. In 1979 the proportion of NPV-infected larvae was positively correlated with population density, which was highest in the wettest part of the study area. In both seasons the proportion of SFB-infected larvae was negatively correlated with population density. Larvae infected with the NPV or the SFB became pallid at an advanced stage of infection, but, although infected larvae were found throughout the larval period, pallid larvae were only found in the later part. It is suggested that larvae become infected in an early instar, then the infections slowly develop throughout the remainder of the larval period. Five larvae were found with mixed infections; four were infected with the SFB and NPV, while the fifth was infected with the SFB and TIV.     

Use of freeze-dried microalgae for rearing gilthead seabream, Sparus aurata L., larvae. II. Biochemical composition

The objectives of this study were to test whether freeze-dried microalgae are nutritionally adequate for rearing rotifers as food for gilthead seabream larvae. The elemental composition (C, N, H) and fatty acid composition were analysed in larvae of gilthead seabream, Sparus aurata L., rotifers Brachionus plicatilis and Brachionus rotundiformis and freeze-dried microalgae Nannochloropsis oculata. Four larval feeding treatments were tested: (A) larvae fed rotifers cultivated with freeze-dried microalgae and daily addition of freeze-dried microalgae to the larval tanks; (B) larvae fed rotifers cultivated with freeze-dried microalgae and daily addition of live microalgae to the larval tanks; (C) larvae fed rotifers cultivated with freeze-dried microalgae, without addition of microalgae to the larval tank and (D) larvae fed rotifers cultivated with live microalgae and daily addition of live microalgae to the larval tanks. No significant differences were observed between the biochemical composition of larvae with treatment A (with freeze-dried microalgae) and the composition of larvae in treatment D that were obtained with the acceptable methods for culture systems (with live microalgae).     

Sublethal effects of a new antifouling candidate on lumpfish (Cyclopterus lumpus L.) and Atlantic cod (Gadus morhua L.) larvae

Sublethal effects of medetomidine, a new generation antifouling compound, on lumpfish (Cyclopterus lumpus L.) and cod (Gadus morhua L.) larvae were examined. The effects on respiration rate and on colour adaptation of newly hatched larvae were assessed after 24-96 h exposure. Exposure of lumpfish larvae to the experimental concentrations resulted in a significant decrease in respiration rate (Lowest Observed Effect Concentration (LOEC) = 5-10 nM) and in the percentage of dark larvae (LOEC = 4 nM). However, no effects on respiration rate of cod larvae were detected. In addition to lumpfish larvae being affected at low concentrations of medetomidine, a reversibility of the effects was observed when 96 h-exposed larvae were incubated in clean seawater for 24-48 h. Considerations relating to the future commercialisation of medetomidine for antifouling purposes are discussed.     

Algae as first food for cod larvae,Gadus morhuaL.: filter feeding or ingestion by accident?

Cod larvae. Gadus morhua L., 24 days posthatch, were fed different species of algae in order to evaluate both rates and mechanisms of ingestion. The results were compared with cod larvae feeding on a natural assemblage of algae in a lagoon. Small algae (Nannochloris atomus Butcher, 14 pm) were found to enter the larval gut in accordance with drinking rate. In contrast, the cod larvae concentrated larger algae [Dunaliella salina (Dunal) Teodor. 6 10 pm] in the gut at rates from 492 to 7251 times the drinking rate. D. salina was captured in the slits between the visceral arches, and increased activity when the algae was added indicate that the cod larvae are active filter feeders during early larval stages. In the gut of cod larvae from the lagoon the fraction of algal material with diameter larger than 8 pm was 39.2% in 7-day-old larvae while, in 12-day-old larvae it had decreased to 12.6%. The most conspicuous characteristics of gut content in the youngest larvae were green spheres (10 μn) and a naked dinoflagellate (20 μn). Short chains of the diatom Skeletonemu cosrarum (Greville) Cleve were also frequently found.     

Calcium localisation by X-ray microanalysis and fluorescence microscopy in larvae of zooxanthellate and azooxanthellate corals

X-ray microanalysis and fluorescence microscopy (Calcium Orangetrade mark) was used to determine the distribution of intracellular calcium (I(Ca)), in the form of total and ionic calcium respectively, in planulae and settled larvae of a zooxanthellate coral. The distribution of total calcium only was determined in larvae of an azooxanthellate coral. In azooxanthellate planulae and settled larvae, total I(Ca) concentration in the oral ectoderm was high and similar to that in seawater (SW). Calcium concentration did not vary (P > 0.05) between planulae and settled larvae. However, settled larvae accumulated large amounts of calcium in gastrodermal lipid-containing cells. In contrast, zooxanthellate planulae possessed significantly (P < 0.01) lower concentrations of total I(Ca) within ectodermal cells in comparison to settled larvae. In addition, in settled zooxanthellate larvae total calcium concentration in the mesogloea and coelenteron was significantly (P < 0.05) higher than in the oral ectodermal and gastrodermal cells, respectively. Total I(Ca) concentrations in the oral ectoderm of settled larvae were also significantly (P < 0.01) lower than that of the calicoblastic ectoderm. In zooxanthellate settled larvae, ionic I(Ca) levels in the aboral epithelium surrounding rapidly growing septa were high. These levels increased significantly (P < 0.05) within the tissue surrounding growing septa after incubation in high-calcium SW.     

Anopheles stephensi and Toxorhynchites amboinensis: aseptic rearing of mosquito larvae on cultured cells

Aseptic larvae of Anopheles stephensi and Toxorhynchites amboinensis were reared on a continuous cell line (RU TAE 12 V) from the mosquito, T. amboinensis, that grew in suspension as multicellular vesicles. Surface-sterilized eggs were hatched in a 24-well plate containing 0.2 ml of Leibovitz's L-15 medium per well and incubated in a humidified atmosphere. Toxorhynchites amboinensis eggs of 36 hr or older were placed singly to assure hatching and avoid cannibalism. Hatching rates were over 80%. All larval instars were maintained in L-15 medium at 28 C with a 12-hr photoperiod. Anopheles stephensi larvae were reared in 25-cm2 tissue culture flasks containing 10 ml of L-15 medium with 30 to 50 first and second instar larvae or 10 third and fourth instar larvae per flask. Toxorhynchites amboinensis larvae remained in the 24-well plate in 1.5 ml of medium through the second instar; third instar larvae were kept in 12-well plates (3 ml of medium per well) and transferred to 25-cm2 flasks (10 ml per flask) when they reached the fourth instar. First and second instar A. stephensi larvae were fed cultured cells once, and third or fourth instar larvae twice a day. Toxorhynchites amboinensis larvae were fed vesicles once during the first 4 days after hatching, and every 1 or 2 days thereafter. Each A. stephensi larva consumed approximately 2 X 10(6) cells, and T. amboinensis larvae 10 times more cells before pupating. Anopheles stephensi pupated after 7 to 8 days and adults emerged during days 9 to 11. Pupation in T. amboinensis began on day 21 after hatching and adults emerged 5 days later. Cell lines isolated from A. stephensi larvae or embryos of the ticks Rhipicephalus sanguineus and Anocentor (Dermacentor) nitens supported only limited growth of A. stephensi larvae. Defibrinated hamster (Mesocricetus auratus) blood, though readily ingested, did not support the growth of A. stephensi whereas larvae reared on blood cells plus T. amboinensis cells showed limited growth.     

Infection by the microsporidium Vairimorpha necatrix (Microspora: Microsporidia) elevates juvenile hormone titres in larvae of the tomato moth, Lacanobia oleracea (Lepidoptera: Noctuidae)

The effects of infection by a microsporidium, Vairimorpha necatrix (Kramer), on the endogenous levels of juvenile hormones in tomato moth (Lacanobia oleracea L.) larvae were investigated. Levels of juvenile hormone II (JH II) were 10-fold greater in the infected larvae on day two of the sixth stadium but no significant difference was observed on day seven. Juvenile hormone I (JH I) was also detected in day two and day seven sixth instar infected larvae but was not detected in non-infected larvae. The duration of the fifth and sixth stadia was significantly longer for infected larvae when compared with non-infected larvae. No evidence was found to suggest that supernumerary moults are a feature of infection by V. necatrix in L. oleracea larvae. Experiments were performed to determine whether the elevation in JH levels, which probably prevents pupation, is an adaptive mechanism of the microsporidium for extending the growth phase of the host, thereby allowing increased spore production. A proportion of infected larvae were collected on days 9 and 24 of the sixth stadium and spore extracts prepared from each larva. These days represent the average duration of the sixth stadium required for uninfected larvae to reach pupation, and the average number of days that V. necatrix-infected larvae survive in the sixth stadium before dying from infection. The mean spore yields from infected larvae 24 days into the sixth stadium were significantly higher than the spore yields obtained from day nine sixth instar larvae. The hypothesis that V. necatrix manipulates host endocrinology (i.e. prolong the host larval state to maximise spore yield) is discussed in context with the results obtained.