Influence of egg size on embryos and larvae of Fundulus heteroclitus (L.)

Egg size for Fundulus heteroclitus (L.) populations is concordant with the distribution of the two F . heteroclitus subspecies, i.e. F. h. heteroclitus eggs are considerably larger than F. h. macrolepidotus eggs. The influence of egg size on survival of embryos during incubation and survival and growth of newly-hatched larvae was estimated for four populations representing both subspecies along the Atlantic coast of the United States and in Delaware Bay. Survival of embryos was determined for incubation periods of 14, 21 and 28 days. Greatest differences in survival were detected following the longest incubation period where less than 50 per cent of the smaller F. h. macrolepidotus eggs survived while little or no mortality was detected among the larger F. h. heteroclitus eggs . Influence of egg size on larval survival was also greatest among those larvae hatched after 28 days where F. h. macrolepidotus larvae survived without food, for an average of 6 days, while F. h. heteroclitus larvae survived 11–12 days. F. h. heteroclitus larvae were significantly larger at hatching than F. h. macrolepidotus larvae. Larval growth rates were the same (0.4 mm day⁻¹) in both subspecies. As a result, size differences at hatching were still maintained after 42 days of growth. The differences in egg size along with other morphological and reproductive characteristics of F. heteroclitus populations probably represent genetically based adaptations to environmental conditions, of which the length of the spawning season is one of the major components stimulating the coevolution of these traits.     

Muscle growth in yolk-sac larvae of the Atlantic halibut as influenced by temperature in the egg and yolk-sac stage

Atlantic halibut eggs and yolk-sac larvae were incubated at 1, 5 and 8° C. Eggs incubated at 8° C gave slightly shorter larvae at hatching with a significantly smaller total cross-sectional area of white muscle fibres than eggs incubated at 5° C. Transport of eggs 2 days prior to hatching gave significantly longer larvae at hatching with a significantly larger red fibre cross-sectional area than when eggs were transported shortly after the blastopore closure. A higher survival until 230 degree days after hatching was also observed in the former group. All eggs incubated at 1° C died before hatching and all larvae incubated at 1° C died before 45 degree days after hatching. From hatching until 230 degree days the total white cross-sectional area increased threefold in all temperature groups. The increase in white cross-sectional area was entirely due to hypertrophy between hatching and 150 degree days (10 mm L _S). Recruitment of new white fibres increased in germinal zones at the dorsal, ventral and lateral borders of the myotome from 150 degree days onwards, but at 230 degree days (12–13 mm L _S) the recruitment fibre zone constituted <10% of the total white cross-sectional area. Larval incubation at 8° C gave slightly longer larvae with a significantly larger cross-sectional area of recruitment fibres at 230 degree days than incubation at 5° C. The larval group incubated at 8° C also had a significantly lower survival until 230 degree days than did the 5° C group. Incubation temperature regimes did not affect the volume density of myofibrils in the axial muscle fibres at 230 degree days. Thus hypertrophy is the predominant mechanism of axial white muscle growth in Atlantic halibut yolk-sac larvae and an increased rearing temperature during the yolk-sac stage increases white muscle fibre hyperplasia.     

Sequestration and Transfer of Cry Entomotoxin to the Eggs of a Predaceous Ladybird Beetle

In the past 10 years, sequestration of Cry toxins and transfer to offspring has been indicated in three insect species in laboratory studies. This work directly demonstrates the sequestration and intergenerational transfer of Cry1F by the parents of the aphidophagous coccinellid predator, Harmonia axyridis, to its offspring. Recently emerged adults (10 individual couples/cage/treatment) were exposed during 20 days to aphids (100 Myzus persicae each day) that fed on a holidic diet containing 20 μg/mL Cry1F (and a control-group). Egg batches and neonate larvae were monitored daily, and counted and weighed for immunodetection of Cry1F by ELISA. At the end of the bioassay, the parents were weighed and analyzed by ELISA. Cry1F was detected in the offspring, both eggs and neonate larvae, of exposed H. axyridis adults. On average the neonate larvae had 60% of the Cry1F concentration of the eggs from the same egg batch. The Cry1F concentration in the adults was positively correlated with the concentration in their eggs. These three results provided independent evidence of transfer to offspring. No detrimental effects of Cry1F were observed on the age of first reproduction, total number of eggs laid per female, age-specific fecundity, egg development time, hatching rate, or fertility rate. The occurrence and generality of intergenerational transfer of Cry toxins should be investigated in the field to determine its potential ecological implications.     

印楝素乳油对梨小食心虫的防控效果研究

【目的】探索0.3%印楝素乳油对梨小食心虫Grapholita molesta的控制效果。【方法】根据梨小食心虫的生物习性,采用浸渍法和浸虫法对梨小食心虫1日龄、3日龄、5日龄的卵和3龄、5龄幼虫进行了杀虫活性测定,采用药膜法对梨小食心虫初孵幼虫进行毒力测定,并通过田间试验测定0.3%印楝素乳油对梨小食心虫的控制效果。【结果】0.3%印楝素乳油对梨小食心虫1日龄、3日龄和5日龄卵的致死中量分别为6.5195、4.5789、6.6268 mg/L,对初孵幼虫的致死中量为6.0495 mg/L,效果较好,而对3龄和5龄幼虫几乎没有杀伤作用。使用有效成分为2.0 mg/kg~3.0 mg/L的印楝素乳油在田间进行梨小食心虫防治试验时,药后5 d和10 d的防治效果在63.18%~76.22%之间,至药后15 d时,防效则下降到27%以下,果实受害明显,表明该药剂已失去控制作用。【结论】印楝素乳油不能作为防治梨小食心虫的专用药剂,仅可在其发生危害的初期,防治其他害虫时,作为兼治的药剂来使用。     

Transovarial passage of Leishmania infantum kDNA in artificially infected Rhipicephalus sanguineus

Phlebotomine sand flies are the only proven biological vectors of Leishmania parasites. However, Rhipicephalus sanguineus ticks have long been suspected to transmit Leishmania infantum in studies carried out in laboratory and natural conditions. In the present study, 5 μl of L. infantum promastigotes (1 × 10⁶ cells per ml) was injected into the hemocel through the coxa I of four engorged females (F1, F2, F3 and F4). Control ticks (F5 and F6) were injected with sterile phosphate-buffered saline (PBS) using the same procedure. Then, these females, their eggs, and the originated larvae were tested by real time polymerase chain reaction (real-time PCR) for the presence of L. infantum kinetoplast DNA (kDNA). Females and eggs were tested after the end of the oviposition period (about 5 weeks post-inoculation) whereas larvae were tested about 4 months after the inoculation of females. All artificially infected females were positive for L. infantum kDNA. In addition, two pools of eggs (one from F2 and other from F4) and four pools of larvae (one from each F1 and F4 and two from F2) were positive for L. infantum kDNA. These results showed, for the first time, the transovarial passage of L. infantum kDNA in R. sanguineus ticks, thus suggesting that the transovarial transmission of L. infantum protozoa in ticks is worth to be investigated.     

Euplectrus melanocephalus Girault (Hymenoptera: Eulophidae), an ectoparasitoid of larvae of fruit-piercing moths (Lepidoptera: Noctuidae: Catocalinae) from northern Queensland

Euplectrus melanocephalus is a gregarious, primary ectoparasitoid of larvae of the fruit-piercing moth genus Eudocima Billberg (Noctuidae: Catocalinae). In northern Queensland, E. melanocephalus parasitised second- and third-instar larvae of Eud. aurantia (Moore), Eud. cocalus (Cramer) , Eud. fullonia (Clerck), Eud. iridescens (Lucas), Eud. jordani (Holland) and Eud. materna (L.). In the laboratory, E. melanocephalus also parasitised Eud. salaminia (Cramer) but failed to oviposit on larvae of two other noctuids, Erebus terminitincta (Gaede) (Catocalinae) and Spodoptera litura (F.) (Amphipyrinae). When parasitising Eud. materna , eggs of E. melanocephalus were deposited dorsolaterally on one of the first five abdominal segments of second- and third-instar larvae. Fourth instars were occasionally parasitised when the density of parasitoids was increased, but successful development to adults was markedly reduced. Pupation took place between the leaf substrate and host. Female parasitoids provided with honey survived 21 days (range = 1–42) and deposited 112 eggs (range = 11–196), while development from egg to adult occupied 12–13 days at 25°C. The minimum temperature threshold for oviposition was 17.5°C, while minimum and maximum development thresholds for larvae were 18.5°C and 30°C, respectively. Studies on the parasitoid/host interactions of E. melanocephalus indicate that it is adapted principally to the larvae of Eudocima spp.     

Uptake and Transfer of a Bt Toxin by a Lepidoptera to Its Eggs and Effects on Its Offspring

Research on non-target effects of transgenic crop plants has focused primarily on bitrophic, tritrophic and indirect effects of entomotoxins from Bacillus thuringiensis, but little work has considered intergenerational transfer of Cry proteins. This work reports a lepidopteran (Chlosyne lacinia) taking up a Bt entomotoxin when exposed to sublethal or low concentrations, transferring the entomotoxin to eggs, and having adverse effects on the first filial generation (F1) offspring. Two bioassays were conducted using a sublethal concentration of toxin (100.0 ng/µl Cry1Ac) for adults and a concentration equal to the LC10 (2.0 ng/µl Cry1Ac) for larvae. Cry1Ac is the most common entomotoxin expressed in Bt cotton in Brazil. In the adult diet bioassay there was no adverse effect on the parental generation (P0) adults, but the F1 larvae had higher mortality and longer development time compared to F1 larvae of parents that did not ingest Cry1Ac. For the 3rd instar larvae, there was no measurable effect on the P0 larvae, pupae and adults, but the F1 larvae had higher mortality and longer development time. Using chemiluminescent Western Blot, Cry1Ac was detected in F₁ eggs laid by P₀ butterflies from both bioassays. Our study indicates that, at least for this species and these experimental conditions, a ∼65 kDa insecticidal protein can be taken up and transferred to descendants where it can increase mortality and development time.     

Ca2+ release from intracellular stores by thapsigargin in sea urchin eggs: Relationship to larval development and relevance in egg activation

Thapsigargin (Tg), an inhibitor of microsomal Ca²⁺ ATPase, is used as a tool to study the changes in Ca²⁺ sequestration in sea urchin eggs and their relationship to embryonic development. Micromolar amounts of Tg inhibit ATP-dependent Ca²⁺ sequestration in a dose-dependent and non-reversible manner, depending on the bulk of biological material used. IC_5O values are 1 nmol/L and 1–10μmol/L, respectively, in the cortical Ca²⁺ stores (isolated cortices preparation) and in digitonin-permeabilized eggs, a preparation giving access to the deeper reticulum compartment. Micromolar Tg does not induce Ca²⁺ release from ⁴⁵Ca pre-loaded cortices but leads to a loss of 25% of the total Ca²⁺ content from the cortical area. Using microspectrofluorimetry of fura-2-loaded eggs, we found that 10 μmol/L Tg induced a moderate rise in cytosolic Ca²⁺ activity as compared with the fertilization-induced Ca²⁺ transient whether eggs were fertilized or not. Early events related to fertilization as, for example, elevation of the fertilization envelope, proton excretion and sustained increase of amino acid uptake, are triggered by 10μmol/L Tg but with a delayed onset relative to sperm-induced effects. The present findings indicate that although it triggers most fertilization-related events, Tg cannot be considered as a true mitotic agent in sea urchin eggs. When added after fertilization, Tg affects cleavage and the further embryonic development giving rise to abnormalities comparable to the animalized larvae obtained with other compounds responsible for the inhibition of reticular Ca²⁺ sequestration.     

Metallothionein induction in early larval stages of tilapia (Oreochromis mossambicus)

Amounts of whole-body metallothionein (MT) in tilapia (Oreochromis mossambicus) larvae increased to a peak (1,500 ng mg(-1) protein) 1 d after hatching (H1), decreased rapidly thereafter, and was maintained at a constant level (700 ng mg(-1)) 3 d after hatching (H3). Waterborne Cd(2+) could stimulate MT expression in newly hatched (H0) larvae in dose-dependent and time-dependent patterns. H0 larvae, which were treated with 35 microg L(-1) Cd(2+) for 24 h, showed a 1.7-fold increase in the MT amount (174.0+/-64.7) and a 6. 5-fold increase in accumulated Cd(2+) but no significant change in Ca(2+) content, compared with the H0 control (MT, 102.6+/-48.1). H3 larvae with the same treatment revealed about a 10-fold increase in accumulated Cd(2+), a 10% decrease in Ca(2+) content, but no change in MT (261.2+/-120.0), compared with the H3 control (MT, 330+/-74.0). H0 larvae could synthesize more MT to bind Cd(2+) for detoxification in 35 microg L(-1) Cd(2+), a dose that would not affect normal physiology or survival of H0 larvae. On the other hand, 35 microg L(-1) Cd(2+) caused H3 larvae to experience hypocalcemia, an abnormal physiological condition, in which H3 larvae could not synthesize sufficient MT, thus causing greater than 25% mortality. These results indicate for the first time that the inducibility of MT by waterborne Cd(2+) is development dependent, being correlated with inconsistent sensitivities to Cd(2+) during larval development.     

Biological studies of the Australian predatory mite Typhlodromalus lailae (Schicha) (Acari: Phytoseiidae)

Abstract The biology of the Australian phytoseiid mite Typhlodromalus lailae is described from material collected in Western Australia and New South Wales in 1994. At 25°C, when fed on cumbungi ( Typha sp.) pollen, the life cycle is completed in approximately 6 days, with an intrinsic rate of natural increase ( r _m ), of 0.38. Female−male pairs produced a mean total of 44.6 eggs within 22 days of oviposition, with 39% of these females living in excess of 29 days. Females that were deprived of males after first mating stopped laying eggs after 4−9 days, but if another male was added they resumed egg laying and produced close to a full complement of eggs (mean 42 eggs). At 25°C, fecundity on a diet of cumbungi pollen or thrips larvae (first-instar Frankliniella schutzei Trybom) was high, averaging 3.71 and 3.33 eggs per day, respectively, over a 3-day period. The sex ratio was approximately 1.5 females to 1 male. Consumption rate of thrips was also high, with an average of approximately seven first-instar or two second-instar F. schultzei larvae eaten per day. The species was also observed to feed on broad mite, Polyphagotarsonemus latus (Banks), and tomato russet mite, Aculops lycopersici (Massee). No diapause was observed under conditions of 25°C 8 h light and 10°C 16 h dark. Eggs were sensitive to low humidity, with 50% failing to hatch below 71.1% relative humidity. This species is of interest as a candidate biological control agent for thrips, broad mite and tomato russet mite in protected crops.     

Larval survival and feeding by immature Metaseiulus occidentalis,Neoseiulus fallacis,Amblyseius andersoni and Typhlodromus pyri on life stage groups of Tetranychus urticae Koch and phytoseiid larvae

When 20 newly hatched larvae either of Metaseiulus occidentalis (Nesbitt), Neoseiulus fallacis (Garman), Amblyseius andersoni Chant or Typhlodromus pyri Scheuten were held in arenas without food at 95% RH and 20°C, the percentages of mites surviving to protonymphs were 5.0, 81.3, 86.3, and 83.8%, respectively. Unfed M. occidentalis larvae starved within 2–3 days, while immatures of the other three species lived up to 12–14 days, with some becoming adults by cannibalizing and/or scavenging. Phytosciid larvae given eggs, larvae/protochrysalis/protonymphs (L/P), deutochrysalis/deutonymphs (D) or teleiochrysalis/female adult (T/A) of Tetranychus urticae Koch, fed at different incidences during 6 h tests. Larvae of T. pyri never fed, but almost all larvae of M. occidentalis fed on eggs and L/Ps and 60–70% of M. occidentalis larvae fed on Ds and T/As. N. fallacis and A. andersoni larvae fed at incidences from 20–75% depending on the stage of spider mite given. Larvae fed more commonly on eggs and L/Ps than Ds and T/As for M. occidentalis and N. fallacis but not A. andersoni. Protonymphs and deutonymphs of all four species, readily fed on T/As after 3 h of exposure, but incidences were higher for A. andersoni and T. pyri. Feeding on phytoseiid larvae by protonymphs and deutonymphs also was more common for A. andersoni and T. pyri. Except for M. occidentalis, deutonymphs fed more than protonymphs on phytoseiid larvae. Results are discussed in relation to individual species life histories and the value of these traits in predicting a species role in a biological control system.     

Evaluation of a granular formulation containing Metarhizium brunneum F52 (Hypocreales: Clavicipitaceae) microsclerotia in controlling eggs of Aedes aegypti (Diptera: Culicidae)

We evaluated the potential of a granular formulation of Metarhizium brunneum F52 containing microsclerotia (MbMSc granules) for control of Aedes aegypti by targeting eggs. MbMSc granules produced infective conidia within 14 days after application to 2.5?g moist potting soil, producing 5.9?×?10⁵, 2.08?×?10⁶ and 6.85?×?10⁶ conidia from 1, 5 and 25?mg MbMSc granules, respectively. Application of MbMSc triggered premature eclosion of eggs (EC_50?=?12?mg) with percentages as high as 31?±?2.9% and 67?±?4.3% of the eggs treated with 5 and 25?mg MbMSc granules, respectively, after 14 days on moist filter paper. Premature eclosion of eggs started at 3 days subsequent to MbMSc granule application and survival of larvae was significantly reduced for granule treated eggs (74?±?2.2%, 39?±?2.0% and 23?±?4.9% larvae survived for 1, 5 and 25?mg granule treatments, respectively, EC₅₀?=?4.9?mg). When MbMSc granules were applied in moist potting soil with mosquito eggs, rates of 1, 5 and 25?mg of MbMSc granules significantly reduced adult emergence with only 81?±?2.1%, 47?±?1.9%, and 34?±?2.1% emergence, respectively (EC₅₀?=?7?mg). Eggs treated with increasing concentrations of fungal conidia enhanced premature eclosion of eggs with an EC₅₀?=?1.6?×?10⁶ conidia/mL. Our results demonstrate that MbMSc granules are a promising candidate for control of A. aegypti and that fermentative production of Mb F52 microsclerotia as the active propagule has the potential for use for mosquito control.     

Brugia malayi: effects of antibacterial agents on larval viability and development in vitro

Recent studies have suggested that intracellular Wolbachia bacteria are necessary for reproduction and survival of adult filarial worms. We now report results of in vitro studies of effects of antibacterial antibiotics (tetracycline, rifampicin, chloramphenicol, azithromycin, and doxycycline) on Brugia malayi infective larvae (L3) motility and molting. All of the antibiotics tested except chloramphenicol decreased L3 motility by 50% or more at 10 days, with minimal effective concentrations (MECs) of 20-100 microg/ml. Tetracyclines, rifampicin, and chloramphenicol inhibited L3 to L4 molting by 12 days in a concentration- and time-dependent manner, with MECs in the range of 1-20 microg/ml. These studies show that antibiotics active against Rickettsiaceae inhibit B. malayi L3 molting at low concentrations in vitro; higher concentrations kill the larvae. While it is possible that antibiotics directly affect filarial L3, we believe it is more likely that the effects seen are indirect effects related to bacterial killing.     

脱氧鬼臼毒素对美洲大蠊的毒力及几种酶系的影响

采用药膜法测试了脱氧鬼臼毒素对美洲大蠊Periplaneta americana初孵若虫的触杀活性,并测定了其对成虫中枢神经系统乙酰胆碱酯酶（AChE）和腺苷三磷酸酶(ATPase)离体活性的影响。结果表明：脱氧鬼臼毒素对美洲大蠊初孵若虫具有较强的毒杀活性,在接触时间24、48、72和96 h 的LC₅₀分别为26.26、4.68、1.51和0.62 μg/cm²;其对AChE没有明显影响; 对Na⁺ -K⁺ -ATPase有明显抑制作用,并存在浓度 效应关系,IC₅₀为44.9 μmol/L; 对Ca²⁺-Mg²⁺-ATPase表现出低剂量激活,高剂量抑制的现象。结果提示美洲大蠊的AChE不是脱氧鬼臼毒素靶标,而ATPase可能是脱氧鬼臼毒素的重要靶标之一。     

Preliminary results of providing various combinations of live foods to grouper (Epinephelus coioides) larvae

Fertilized oyster eggs, S-rotifer (Brachionusrotundiformis) and SS-rotifer (Brachionus sp.),were tested either solely or in combination fortheir suitability as feed for early stage grouper (Epinephelus coioides) larvae. Sizes ofS-rotifers ranged between 143-224 µm lorica lengthwith mean 182±21µm, and SS-rotifersbetween 122-176µmlorica length with mean 154±13µm. Theresults indicated that both fertilized oyster eggs andSS-rotifers were suitable as feed at F1 (first feedingday). However, poor growth was recorded when providing oyster eggs solely for the periodsF1-F3. Although growth of larvae at F6 had nodifference between the sole SS-rotifers and the oystereggs additionally provided for F1-F3, better survivalof larvae at F15 was obtained when providingcombinations of SS-rotifers with oyster eggs for F1-F3.Besides, better growth and survival of larvae at F15was found when providing S-rotifers enriched withKirin yeast for F7-F15. The highest survival andfastest growth of larvae at F15 was found whenproviding oyster eggs for F1-F3, SS-rotifers forF1-F6, S-rotifers for F7-F15, both rotifers enrichedwith Kirin yeast, and Isochrysis for F1-F15.Total fatty acid (TFA), EPA, DHA content, and DHA/EPA(D/E) ratio of larvae changed with their sizes andcorresponded to that of their feeds. The F15 larvaehaving a higher TFA grew faster, having higher DHA orEPA survived better.     

Effect of Bacillus thuringiensis Cry1 toxins in insect hemolymph and their neurotoxicity in brain cells of Lymantria dispar

Little information is available on the systemic effects of Bacillus thuringiensis toxins in the hemocoel of insects. In order to test whether B. thuringiensis-activated toxins elicit a toxic response in the hemocoel, we measured the effect of intrahemocoelic injections of several Cry1 toxins on the food intake, growth, and survival of Lymantria dispar (Lepidoptera) and Neobellieria bullata (Diptera) larvae. Injection of Cry1C was highly toxic to the Lymantria larvae and resulted in the complete inhibition of food intake, growth arrest, and death in a dose-dependent manner. Cry1Aa and Cry1Ab (5 microg/0.2 g [fresh weight] [g fresh wt]) also affected growth and food intake but were less toxic than Cry1C (0.5 microg/0.2 g fresh wt). Cry1E and Cry1Ac (5 microg/0.2 g fresh wt) had no toxic effect upon injection. Cry1C was also highly toxic to N. bullata larvae upon injection. Injection of 5 microg/0.2 g fresh wt resulted in rapid paralysis, followed by hemocytic melanization and death. Lower concentrations delayed pupariation or gave rise to malformation of the puparium. Finally, Cry1C was toxic to brain cells of Lymantria in vitro. The addition of Cry1C (20 microg/ml) to primary cultures of Lymantria brain cells resulted in rapid lysis of the cultured neurons.     

甲醛致酵母菌与大肠杆菌DNA-蛋白质交联作用的比较

为了探讨甲醛致真核生物与原核生物DNA-蛋白质交联(DNA-protein crosslinks,DPC)的作用,以毕赤酵母(Pichia pastoris)和大肠杆菌(Escherichia coli)DH5α为材料,采用KCl-SDS沉淀法检测液态甲醛染毒后酵母菌与大肠杆菌中DPC含量。结果表明,低浓度(25μmol/L)甲醛不能引起酵母菌和大肠杆菌的DPC(P>0.05),而较高浓度(125和625μmol/L)甲醛可引起酵母菌和大肠杆菌明显的DPC(P<0.05);另外,酵母菌的DPC系数是大肠杆菌的DPC系数的10倍左右。这表明甲醛致真核细胞和原核细胞的DPC作用具有剂量效应关系,而且真核细胞的DPC系数比原核细胞的DPC系数更高。     

Some notes on the ecology of a GermanBranchipus schaefferi population (Crustacea: Anostraca)

Habitat preference, seasonal occurrence, starvation resistance, hatching eggs ofBranchipus schaefferi, and effects of predation onB. schaefferi were studied.Branchipus was only present in turbid, unvegetated ponds and absent in ponds which contain higher aquatic vegetation and theSpirogyra sp. The first individuals ofB. schaefferi appeared in April when water temperature was 10 °C and the last adults in November at a water temperature of 3.5 °C. Up to 6 reproducing generations were observed during this period. Abundance ofB. schaefferi was higher in temporary ponds than in permanent ponds. Sex ratio was close to unity for most of the year. Body size ofB. schaefferi males and females was significantly positively correlated with pond volume. Without foodB. schaefferi could survive for 1.5 to 2 days at 20 °C and 4 to 5 days at 10 °C. Hatching success of eggs decreased when eggs were dried for 7 months. Freezing of eggs had no effect on hatching success. From] the predators tested,Chaoborus sp. larvae clearly selected smallB. schaefferi; one consumed approximately 6Branchipus d–1 at a density of 6 to 12 prey 1–1. The other predators, dragonfly larvae, and larvae and adults ofTriturus alpestris selected alternative prey types, for exampleTubifex sp. and ostracods.     

Effect of egg dosage and host genotype on liver trapping in murine larval toxocariasis

In this study we examined the effect of various initial sensitizing doses of infective Toxocara canis eggs and the effect of murine host genotype on the level of trapping of larvae in the liver after larval challenge. In the initial experiments, C57BL/6J mice were infected with a sensitization dose of 5, 25, 75, 125, or 250 infective T. canis eggs on day 0 postinfection (PI). On day 28 PI all mice were challenged with 500 infective eggs. On days 7, 14, and 21 postchallenge (PC) larval numbers within individual livers were determined. Trapping of larvae was observed in mice receiving a sensitization dose of 25 or more eggs. At 7 and 14 days PC the level of trapping increased with sensitization egg dose up to a dose of 125 eggs. At 21 days PC the level of trapping reached a plateau at a sensitization dose of 75 eggs. The peak level of larval trapping was observed on day 7 and day 14 PC following sensitization doses of 125 and 250 eggs, respectively. In the subsequent experiments, mice of various strains and H-2 haplotypes were inoculated with an initial sensitization dose of 125 eggs and a challenge dose of 500 eggs on day 0 and day 28 PI, respectively. Larval trapping within the liver was determined on day 14 PC. C57BL/6J mice trapped significantly more larvae than DBA/2J mice (P less than 0.01); all other strains trapped larvae at a lower, but statistically similar, level to the C57BL6/J mice.(ABSTRACT TRUNCATED AT 250 WORDS)     

The development of Eustrongylides tubifex (Nematoda: Dioctophymatoidea) in oligochaetes

Egg development of Eustrongylides tubifex (Nitzsch in Rudolphi, 1819) J?gerski?ld, 1909, was studied at 5, 10, 15, 20, 25, and 30 C. Eggs developed at 20, 25, and 30 C. Development ceased at 0, 5, 10, and 15 C but resumed when temperatures were raised. Eggs contained first-stage larvae in 23-26 days at 25 C. Seven species of aquatic oligochaetes were exposed experimentally to eggs of E. tubifex containing first-stage larvae. Third-stage larvae of E. tubifex developed in the aquatic oligochaetes, Limnodrilus hoffmeisteri Claparède, 1862, and Tubifex tubifex (Müller, 1774). Larvae developed in the ventral blood vessel of oligochaetes. Second-stage larvae were seen first in oligochaetes 30 days postinfection and third-stage larvae were seen 70-109 days postinfection at 25 C. Third-stage larvae in oligochaetes retained the cuticle of the first and second molt.