Factors affecting oviposition and fecundity in the grain miteAcarus siro L. (Acarina:Acaridae), especially temperature and relative humidity

Oviposition and fecundity in the grain miteAcarus siro were studied at 5–30°C and 62.5–90% RH. At and above 20°C, 80% RH, mating and oviposition occurred soon after emergence, but at lower temperatures and humidities egg laying was progressively delayed from one to several days. Females needed to mate repeatedly in order to achieve maximum egg production, optimum conditions for which were 15°C, 90% RH, where total output per female averaged 435 with a maximum of 858. Oviposition rates were highest at higher temperatures, the mean daily rate at 20 and 25°C, 90% RH, rising to maximum levels of 28/29 eggs per female per day on day six.Oviposition followed clearly defined patterns, favourable conditions producing rapid increases in the mean daily oviposition rate to high peak levels reached at an early stage in the oviposition period. Less favourable conditions resulted in reduced outputs and lower, more uniform rates of egg laying. The mean oviposition period, varying with humidity, fell from 72–122 days at 5°C to 9–13 days at 30°C and the mean incubation period from 42–70 days at 5°C to 3–4 days at 30°C. Egg viability increased with increasing humidity but was little affected by temperature and unaffected by age of the female at time of oviposition.Males tended to live longer than females at most conditions; longevity—depending on humidity—averaging 13–15 days at 30°C and 129–175 days at 5°C. Adult life for females averaged 12–19 days at 30°C and 88–169 days at 5°C. An index of suitability, calculated from egg number, viability and duration of the egg stage and oviposition period, indicated that the most favourable conditions for oviposition and hatching were 20–25°C and 80–90% RH.     

Effect of temperature on the ovipositional biology and egg viability of the cattle tickBoophilus annulatus (Acari: Ixodidae)

The effect of temperature on the ovipositional biology ofBoophilus annulatus (Say) was determined under laboratory conditions. Engorged females subjected to constant temperatures of 12 and 45°C died without ovipositing, while females held at 15 and 40°C laid eggs which did not hatch. The preoviposition period at 25–40°C was 2–3 days; however, significant increases occurred at 20°C (5.2 days) and at 15°C (16.3 days). The number of eggs laid per female was ca. 2700 at temperatures of 25–35°C, but decreased significantly at 20°C (ca. 2300 eggs/female), 15°C (ca. 1800 eggs/female), and at 40°C (ca. 300 eggs/female). No differences were observed in the Conversion Efficiency Index (CEI) values at temperatures of 20–30°C (ca. 50%), while temperatures of 15 and 40°C produced the lowest CEI values at 35.6 and 4.9%, respectively. Hatch-ability of eggs was ca. 80% at temperatures of 20–35°C. Incubation period of eggs ranged from 52.2 days at 20°C to 16.2 days at 35°C. The thermal threshold for egg development determined by linear regression was 12.9°C. Females subjected to four fluctuating temperature regimes produced no differences in number of eggs/female (ca. 2400), CEI (ca. 50%), or hatchability of eggs (ca. 75%). Preoviposition period and incubation were significantly affected by a change in the thermoperiod, becoming longer in duration as the temperatures were decreased. From studying females exposed for various intervals from 0 to 105 days at 12°C, indications were that the longer the exposure period the more adverse the effects were on oviposition and egg-hatch. Correspondingly, exposure of eggs to a temperature of 15°C for up to 105 days gave indications that the longer the eggs remained at 15°C, the lower the hatch would be after transfer back to a temperature of 25°C.     

Biology of Ixodes Rubicundus Ticks under Laboratory Conditions: Observations on Oviposition and Egg Development

Observations on oviposition and egg development of Ixodes rubicundus were made under laboratory conditions. Engorged females were exposed to temperatures in the range 10–25°C and relative humidities (RHs) of 33 and 93%. The pre-oviposition period, oviposition period, incubation period, conversion efficiency index (CEI) values and fecundity were determined. The mean pre-oviposition period varied from 13.3 days (temperature 25°C and RH 33%) to 68.3 days (temperature 10°C and RH 93%). Oviposition extended from a mean of 39 days (temperature 25°C and RH 93%) to 201.7 days (temperature 10°C and RH 93%). The developmental zero temperature for the pre-oviposition period was 9.2°C. The mean total number of eggs produced by engorged I. rubicundus females varied from 2045.7 (temperature 10°C and RH 93%) to 3777.7 (temperature 20°C and RH 93%). Both female mass and RH significantly (p < 0.01) influenced the number of eggs produced. CEI values varied between 43.1–54.4% (RH 93%) and 34.1–42.5% (RH 33%). At 93% RH females produced between 14.2 and 17.7 eggs per mg body mass compared to the 13.2–14.6 eggs per mg body mass at 33% RH. The shortest mean incubation period recorded was 164.3 days (temperature 25°C and RH 93%). The developmental zero temperature for incubation was 6.5°C. Both the pre-oviposition and oviposition periods of I. rubicundus are more extended compared to other species of the genus. Ixodes rubicundus produces a large number of small eggs compared to other prostriate ticks.     

Laboratory studies of factors affecting egg hatch of triops longicaudatus (LeConte) (Notostraca : Triopsidae)

Egg hatch was greatest (78.33%) for eggs not previously desiccated. A reduction in numbers hatched occurred as the relative humidity at which they were dried decreased. Some eggs hatched (0.67–79.33%) at pH levels of 3.10–10.01 with the highest hatch at pH 5.60. Water temperature greatly affected egg hatch. No hatch occurred until temperatures were above 14°C. A constant 29°C significantly inhibited hatching. Egg hatch increased 13.00 to 43.42% as salinity decreased from 2200 to 9.24 micromhos/cm. As little as 13 mm of flooded soil covering the eggs prevented them from hatching for 14 days. Eighteen percent hatch resulted when soil and eggs were redistributed to a 1 mm soil layer. Egg samples from the same parent, even though treated similarly, often hatched at greatly varying rates and only rarely was hatching 100% within a replication.     

Biology of the shore fly Scatella stagnalis in rockwool under greenhouse conditions

The development times and survival of immature stages in rockwool and the fecundity and longevity of adult Scatella stagnalis were determined and stage-specific life-tables constructed for the species at constant 20 and 25 °C and at a fluctuating temperature (23–34 °C, mean 28.5 °C). Development time from egg to adult decreased with temperature, being 15.9±0.1 days at 20 °C, 11.4±0.1 days at 25 °C and 10.1±0.2 days at fluctuating temperature with mean of 28.5 °C. The lower threshold for egg-to-adult development was 6.4±2.7 °C and the total quantity of thermal energy required to complete development was 212.8±.0 °C. The proportion of females in two populations studied was 0.521. High temperature increased the mortality of pupae from 7% (20 °C) and 10% (25 °C) to 29% at 28.5 °C. At 25 °C, female longevity was 15.5±0.7 days and fecundity 315±19 eggs/female (20.4 eggs/female/day). Males lived for 22.0±1.1 days. At constant 25 °C, the net reproductive rate was 126.1 female eggs/female, generation time was 18.4 days, the doubling time of the population 5.3 days, and the intrinsic rate of increase (r _m) 0.263 day^–1.     

Environmental influences on fecundity, egg viability and egg cannibalism in the scale insect predator, Chilocorus nigritus

The effects of temperature on age-specific fecundity, egg viability and egg cannibalism were examined in the coccidophagous coccinellid, Chilocorus nigritus being fed on the cyanophyllum scale, Abgrallaspis cyanophylli. There were no significant differences in lifetime fecundity or oviposition rate at constant temperatures in the range of 20 to 30°C although there was a trend for both parameters to increase with increasing temperatures. Total fecundity ranged from five to 1890 eggs per female whilst the oviposition rate varied from 0.2–12.1 eggs day^-1. Egg viability was significantly greater at 26 and 30°C (63 and 74%, respectively) than at lower temperatures (18 to 30%) whilst egg cannibalism was highest at 24 and 26°C (being the mid range of the temperatures tested). Mean pre-oviposition periods varied from 54 days at 20°C to 8.2 days at 30°C. The effect of relative humidities in the range of 33% to 75% on oviposition rate, egg viability and egg cannibalism was measured and found to have no significant effect on either parameter.     

The influence of temperature and resource level on the fecundity of a predatory planktonic mite,Piona exigua Viets

Summary Piona exigua Viets is a predaceous freshwater mite that can potentially affect the population densities of its cladoceran prey. As part of a study of the effect of Piona exigua on its prey populations we measured the effects of water temperature and prey density on the lifespan, age at first reproduction and per capita egg production of adult female mites. Mites were raised in the laboratory at five prey (Ceriodaphnia, Daphnia) densities (5, 15, 30, 60, 120/l) at 15° C and at four temperatures (10, 15, 18, 22° C) at c. 60 prey/l. In response to increased food level, mites increased the number of eggs laid to reach a maximum at 60 prey/l, the rate at which they were laid increased and the pre-reproductive period was shorter. Low temperatures prolonged the pre-reproductive period. At temperatures above 10° C, food level and temperature had more influence on the timing of reproductive events (growth rate, oviposition rate, age at first reproduction) than on the size of females at first reproduction. When temperatures exceed 10° C and food levels exceed 5 prey/l the major scope for reproductive plasticity in Piona lies in the timing and duration of egg production.     

Effect of incubation temperature on the hatching of rotifer resting eggs collected from sediments

Sediment samples from Loch Leven, Scotland, were incubated at 5°C, 10°C and 15°C to induce hatching of rotifer resting eggs. The emergent animals were identified and counted. The temperature which induced hatching varied among the nine species studied. These results are discussed in relation to seasonality and temperature preferences previously recorded for the most abundant species. Resting egg densities of 2.2–13.9 eggs cm^–3 were recorded in the upper 5 cm of sediment.     

The combined effects of temperature and food consumption on body weight,egg production and developmental time in Chaoborus crystallinus De Geer (Diptera: Chaoboridae)

Summary Chaoborus crystallinus fourth-instar larvae were reared individually at 14°, 17° and 20° C under different food conditions. Daphnia magna of 1.25 mm average length served as prey. The following were measured: amount of prey ingested, larval weight gain, duration of fourth instar, body weight of the adults, and egg number per female. At a given temperature, the body weight, egg-number and developmental rate increased with food consumption. At a given food consumption, higher temperatures caused a decrease in body weight and egg number, and an increase in developmental rate. Gross production efficiencies for fourth-instar larvae were highest at temperatures around 17° C. The results clearly indicate that from an energetic point of view higher temperatures are disadvantageous. In C. crystallinus vertical migration is evidently a way of lowering the temperature to which the animals are exposed and hence optimizing food conversion into biomass and offspring production, especially if prey densities are below the saturation level.     

Reproductive bionomics of the soft tick, Ornithodoros turicata (Acari: Argasidae)

The effects of different temperatures and relative humidities (RHs) were tested on various reproductive parameters of Ornithodoros turicata, an argasid tick that inhabits gopher tortoise burrows in Florida, USA. The pre-oviposition, oviposition and incubation periods of the ticks decreased as temperature increased. These periods were also affected by the RH. The number of eggs oviposited was affected significantly by the combined effect of temperature and RH. Fewer eggs were laid by ticks in the 24°C regimes and the 27°C/95%RH regime compared to those in the other temperature/RH groups. There was an inverse relationship between the number of eggs oviposited and the percentage of hatched larvae that was correlated with the temperature and RH. Ticks reared at 27°C/90%RH and 30°C/90%RH laid more eggs than those reared in the other combinations of temperature and humidity but fewer larvae hatched from these eggs. The reproductive fitness index (RFI) values were highest in females held in the 24°C groups and the 30°C/95%RH group, although significantly more larvae hatched at the lower temperatures. The optimum reproductive conditions for O. turicata under laboratory conditions appear to be 24°C and 90–95%RH. While mating occurred at all temperatures, none of the females laid eggs at 22°C. The ticks may move preferentially to low temperatures when not feeding to remain above the critical equilibrium humidity and/or below the critical metabolic level necessary for prolonged survival. However, most female ticks oviposited after 45 days when moved to 27°C/95%RH. Ornithodoros turicata females may have a limited capability to delay oviposition until an optimal microenvironment for egg deposition can be located in the burrow.     

The influence of exposure to cold on the incidence of gastric ulcers after reserpine in rats

Groups of female rats (n=20) exposed from 0 to 13 days to T_a's from 8.0° to 29.0°C were given 2.5 mg/kg reserpine i.p.; T_re and gastric ulcers (GU) were recorded 24 h afterwards. At exposure temperatures below 21.0°C there was a highly significant positive correlation between T_a and T_re (r=0.85) and a negative correlation between T_a and GU (r=–0.92). The GU rate after reserpine was not affected by temperatures above 21°C up to 29°C. Below 16.5°C a difference of the reserpine response was found between rats with less and more than 3 days acclimation to a given T_a. In rats with less than 3 days acclimation the mean T_re after reserpine was 1.0°C lower and the mean GU rate was 1.7 ulcers/rat higher than in rats with more than 3 days acclimation. The correlation of T_re with GU rate revealed that the mean number of GU increased with decreasing T_re · T_re and GU were negatively correlated in both series of experiments: r= –0.92 for non-acclimated rats and r= –0.95 for >3d acclimated rats. Cold acclimation of rats for 8 days at 13.0 °C or 13 days at 10.0 °C did not significantly affect T_re and the GU rate if the rats were taken to 21.0°C after reserpine administration. The results show that with and without cold-acclimation the extent of hypothermia in rats after a standard reserpine dose depends on the prevailing ambient temperature below the comfort range and the GU rate depends on the extent of the hypothermia.     

Adaptability and efficacy of transgenic and wild-type Metaseiulus occidentalis (Acari: Phytoseiidae) compared as part of a risk assessment

Comparisons between transgenic (T) and wild-type Metaseiulus occidentalis colonies (COS) were made under laboratory conditions as part of a risk assessment effort prior to proposed field releases. There were no differences between the transgenic T18 colony and the COS strain in the daily egg production, hatchability at three temperatures and four relative humidity (RH) conditions, diapause incidence, or proportion of female progeny produced. Metaseiulus occidentalis eggs do not hatch at 38°C under any RH tested, nor at 33.5°C under 100% RH, indicating that high temperature and extreme RH affect egg hatch negatively. At 28.5 and 33.5°C, fewer eggs hatched at 32.5% than at 75.5 and 93% RH. Metaseiulus occidentalis cannot survive on any plant tested without prey nor on a diet of pollen alone; adult female mites cannot prey or survive on a diet of eggs and larvae of two lepidopteran species, indicating that the suitability of food sources has not been altered in the transgenic strain. Two subcolonies, derived from two transgenic strains using single females, differed in the rate of egg hatch at 28.5°C under 32.5 and 100% RH, indicating that reduced genetic variation and/or random genetic drift in the two lines may have led to differences in some biological characters. Since we did not find any significant differences between the T18 and COS colonies in the traits tested, the T18 colony is not expected to exhibit any new biological attributes in a proposed short-term field release.     

Field and laboratory studies on the timing of oviposition and hatching of the western black-legged tick, Ixodes pacificus (Acari: Ixodidae)

The timing of oviposition and hatching of Ixodes pacificus was investigated in the field and at constant temperatures in the laboratory. Replete females held at temperatures between 9 and 29°C began depositing eggs a mean of 9–70 days after drop off. Egg masses held between 12 and 25°C commenced hatching 25–178 days after the onset of oviposition. Eggs held at 9 or 29°C did not hatch. The lower temperature thresholds for development (LTD) for oviposition and hatching were 6.5 and 9°C, respectively. The number of degree days required for oviposition and hatching was 173 and 588, respectively. Replete females placed in the field on 2 December through to 8 March deposited eggs from 2 February through to 24 April; the eggs commenced hatching between 2 July and 21 August. Unfed larvae from two of 20 egg masses survived through the winter and fed readily when exposed to deer mice (Peromyscus maniculatus) on 22 April. Replete larvae were returned to the field and moulted between 9 and 21 August. Larvae exposed to deer mice in August, 4 weeks after hatching, also fed readily. Although further studies are needed to clarify the timing of nymphal development, the present study suggests that I. pacificus requires more than 1 year to complete its life cycle.     

An analysis of diapause and resistance in the egg stage of Floronia bucculenta (Araneida: Linyphiidae)

Summary Floronia bucculenta hibernates in the egg stage; the egg sacs are deposited on the leaves of grass tussocks without any shelter. The morphogenesis of the eggs was divided into 10 arbitrarily chosen stages, in order to test the dependence of embryonic development on temperature in the laboratory. The eggs developed slowly at 23°C, 16°, 12.5°; embryogenesis stopped after 70–45 days, when prosomal appendage rudiments began to form. At 10°, 7.5°, 5°, 0° complete embryogenesis was possible until the emergence of the first complete stage. The eggs developed most rapidly at 5° (mean developmental time 203 days). The egg development was normal at 5° and 0°, when compared with the timetable of the embryogenesis of the linyphiid Bathyphantes gracilis, a species which has no egg diapause. At 7.5° and 10° the embryogenesis was strongly delayed during the median phases of development (elongation of the germ band, formation of prosomal appendages); after reversion the development was accelerated (postdiapause phase). After long exposure to low temperatures (-10° to +10°) the diapause was terminated. A temperature of 0° was optimal (minimal time of exposure 8–9 weeks). The time required for embryonic development of postdiapause eggs decreased hyperbolically with increasing temperature. In the field the median phases of embryogenesis were retarded by low ambient temperatures; diapause was terminated from late December to mid-January. The spread of hatching in spring was 7–15 days.During the diapause phase the O₂-consumption of the eggs at 25° was depressed. It rose from 1.55 (in late diapause) to 4.21 ml/100 eggs·h at the onset of postdiapause, whereas O₂-utilization did not change significantly at 5° (from 0.54 to 0.61 ml/100 eggs·h just after the termination of diapause).The diapause phase was not characterized by higher resistance to cold, drought, or flooding. As compared with single eggs removed from the cocoon, the silken wall of the intact egg sac did not affect the survival of postdiapause eggs exposed to-15° (LD₅₀=28 days); it raised, however, the survival time of eggs exposed to a R.H. of 32% (at 5°) or flooding by distilled water (at 5°): from LD₅₀=37 to 68 days at drought, from LD₅₀=30 to 92 days at flooding.Diapause is important for synchronizing the life-cycle of F. bucculenta with the seasonal fluctuations of environment. The egg stage is highly tolerant to the extreme factors of the winter. Some implications of the relation of the studied spider to its habitat are discussed.     

The predatory mite Hypoaspis miles: biological and demographic characteristics on two prey species, the mushroom sciarid fly, Lycoriella solani, and the mould mite, Tyrophagus putrescentiae

The biology of Hypoaspis miles Berlese (Acarina: Hypoaspidae) fed on mushroom sciarid larvae (Lycoriella solani Winnertz) (Diptera: Lycoriidae) and mould mites (Tyrophagus putrescentiae Schrank) (Acari: Acaridae), was investigated by laboratory experiments at 20 °C, 75% r.h. and LD16:D8 hours. H. miles had a significantly shorter development time and a significantly lower juvenile mortality when fed on sciarid larvae than on mould mites, the development time being 14.5 days and the mortality 3.5% on the former prey. The preoviposition and postoviposition periods of H. miles were not uninfluenced by the prey species and were 5–9 and 32–37 days, respectively. Oviposition periods of 53.2 and 68.5 days and female longevities of 82 and 109.6 days were observed on diets of sciarid larvae and mould mites, respectively. Male longevity (168–219 days) was uninfluenced by the prey species. The egg production of H. miles on sciarid larvae was estimated to be 44.4 ± 4.33 eggs per female, as compared to 22.43 ± 1.79 eggs per female on mould mites. The sex-ratio of the offspring was significantly influenced by the prey species, the ratios (/(+)) being 0.66 on sciarid larvae and 0.54 on mould mites. The net reproductive rate (R₀) for H. miles fed on sciarid larvae was approximately 27 which was three times higher than for mites feeding on mould mites. The innate capacity of increase (r_m) was highest (0.0747 day^–1) when sciarid larvae served as food, giving a doubling time of 9.3 days as compared to 12.8 days on mould mites. The generation times were 44.28 on sciarid larvae and 40.67 days on mould mites. The daily food consumption rate of juvenile and adult H. miles was 0.24 and 0.86 sciarid larvae and 10.8 and 21.7 mould mites, respectively. In terms of weight consumed, however, the consumption of sciarid larvae was 2–3.5 times the weight of mould mites. The ratio of females to males influenced the oviposition period and egg production of H. miles, with virgin females laying fewer eggs over a longer period of time as compared with females with access to males. The egg production in relation to the sex-ratio was described by models predicting a maximum number of eggs per female of 22.3 to be attained at a sex ratio of 0.69 (/(+)) and a maximum daily number of eggs per female of 0.33 to be attained at a sex ratio of 0.37 (/(+)).     

Differences in development time,mortality and water loss between eggs from laboratory and wild populations ofDermatophagoides pteronyssinus (Trouessart, 1897) (Acari: Pyroglyphidae)

A total of four microcultures of adults ofDermatophagoides pteronyssinus, two each from laboratory and wild populations, were fed on separate diets of house dust and yeast granules. A total of 35 eggs of known age from each of the four microcultures were harvested and incubated at 15°C, 60% RH for 16 h/day and 30°C, 75% RH for 8 h/day to simulate diurnal microclimatic fluctuations in a bed. Eggs from females fed on yeast were larger and underwent more rapid rates of water loss, estimated by measurements of reduction in visible surface area (VSA), than eggs from females fed on house dust. There were no significant differences in mean egg development time between the four microcultures (range 6.0–6.88 days). Mortality of the eggs was as follows: from laboratory females fed on yeast, 31.4%; laboratory females fed on house dust, 11.5%; wild females fed on yeast, 2.9%; wild females fed on house dust, 0%. Thus diet and egg size at oviposition had no effect on mortality. Since the microclimates at which eggs from both populations were oviposited and incubated were identical, it is hypothesized that mortality was higer in eggs from laboratory cultures because the mites had become acclimated to the optimal conditions at which they had been kept and were less able to withstand the diurnal fluctuations in microclimate, similar to those imposed upon wild mites in their natural habitats.     

Thermal dependence of reproductive allocation in a tropical lizard

In ectotherms, environmental temperature is the most prominent abiotic factor that modulates life-history traits. We explored the influence of environmental temperature on reproduction in the Madagascar ground gecko (Paroedura picta) by measuring reproductive traits of females at constant temperatures (24, 27, 30 °C). Females of this species lay clutches of one or two eggs within short intervals. For each female, we measured egg mass for the first five clutches. For one clutch, we also measured the energetic content of eggs via bomb calorimetry. Temperature positively influenced the rate of egg production, but females at 30 °C laid smaller eggs than did females at either 24 or 27 °C. Dry mass of eggs scaled allometrically with wet mass, but this relationship was similar among thermal treatments. Females at all temperatures produced eggs with similar energy densities. Females at 24 °C allocated less energy per time unit (≈8 mW) to reproduction than did females from higher temperatures (≈12 mW). However, females at either 24 or 27 °C allocated significantly more energy per egg than did females at 30 °C. Our results demonstrate that a complex thermal sensitivity of reproductive rate can emerge from distinct thermal sensitivities of egg size, egg composition and clutch frequency.     

Reproduction induced by blue light in female gametophytes of Laminaria saccharina

Summary In red light at 15°C, female gametophytes of Laminaria saccharina continue to grow indefinitely without becoming fertile, but 6–12 hours' irradiation with blue light induces the production of eggs. At lower temperatures, some gametophytes become fertile in red light, but blue irradiation increases the percentage of fertile gametophytes.     

Biology, life table and host specificity of the mushroom pest, Brennandania lambi (Acari: Pygmephoroidea)

Biology and life table parameters of Brennandania lambi (Krczal) were studied at different temperatures while feeding on white mushroom (Agaricus bisporus) mycelium cultured on mushroom compost. The duration of egg and larva development, preoviposition and oviposition period, female longevity, and the time to 50% mortality declined as temperature increased from 16 to 28°C. The threshold temperature of development (female) was 9°C and the thermal constant for completion of development (female) was 195 day-degrees. At 16, 20, 24 and 28°C, the total fecundity (eggs/female) was 71, 67, 66 and 57, respectively and the daily fecundity rate (eggs/female/day) was 5.6, 8.7, 8.7 and 9.1, respectively. The sex ratio (female/male) ranged from 1.9 to 2.1 at 16–28°C. At 16, 20, 24 and 28°C, the intrinsic rate of natural increase (r _m) was 0.11, 0.18, 0.22 and 0.27, respectively, and the population doubling time was 6.1, 3.9, 3.2 and 2.5 days, respectively. All life stages of the mite died when exposed to 35°C constant temperature for 24h, or to 32°C constant temperature for 12 days or to 31–35°C (average 32.9°C) ambient temperature for 4 days. Brennandania lambi completed development only when fed on Ag. bisporus mycelium growing on mushroom compost. It could not survive on mushroom mycelia of Auricularia auricula, Au. polytricha, Ganoderma lucidum, Hericium erinaceus, Lentinus edodes, Pleurotus ostreatus, P. sajor-caju and Tremella fuciformis.     

Life cycle of the microbivorous Antarctic Dry Valley nematode Scottnema lindsayae (Timm 1971)

The life cycle of the Antarctic Dry Valley soil nematode, Scottnema lindsayae (Timm 1971) was studied in laboratory culture at two temperatures, 10°C and 15°C. Soil yeast and bacteria isolated with the nematodes were used as the food source. The species reproduced sexually. The higher temperature had a negative effect on the life cycle. The number of eggs per female and the number of juveniles developing per female were greater at 10°C than at 15°C. Juveniles developed faster at 10°C and four juvenile stages were observed outside of the egg at both temperatures. The unusually long life cycle (218 d at 10°C) suggests that more than one austral summer may be required for successful completion. An increase in Dry Valley soil temperatures associated with potential global environmental change may have detrimental effects on soil nematodes.