Ecology of diapausing copepodids of Cyclops kolensis Lill. in reservoirs of the Upper Volga

Cyclops kolensis Lill. forms dense populations in different water-bodies of the Upper Volga basin. In spring, when the other planktonic crustaceans have not yet appeared, C. kolensis is an important food object for fishes. Its active reproduction occurs from April to the beginning of June. A rapid accumulation of stage IV copepodids in the plankton occurs in June and at 12–14° they sink into the pelogene in a diapause stage. During the summer stagnation period the diapausing copepodids are distributed evenly over the bottom; their abundance here is 0.7–0.8 million ind. m^-2 (Rybinsk reservoir). During storms and autumn active water mixing the copepodids together with detritus are disturbed and brought to the deepest, silt rich, part of the water-bodies. After the ice formation and at the beginning of bottom heating the diapausing copepodids are transported by near bottom currents and are concentrated in depressions; their biomass here reaches 60 g m^-3. After the thermo-oxy-cline formation they revive and begin to live actively. Copepodids feed, accumulate adipose matter and in February–March they begin to moult.     

Ultrastructural studies on the early cuticular metamorphosis of adult female Lernaeocera branchialis (L.) (Copepoda,Pennellidae)

After its final moult and fertilization an adult female of the marine fish-parasitic copepod, Lernaeocera branchialis, begins an extensive metamorphosis. This commences while the parasite is still on the flounder intermediate host and is completed once the female has established itself on the whiting final host. One early component of the metamorphosis is a considerable elongation of the parasite's abdominal region. S.e.m. and t.e.m. studies have revealed that part of the mechanism of the elongation consists of a straightening out of a highly folded abdominal cuticle. Before fertilization, the epicuticle and outer procuticular layers of this integument are thrown into a series of transverse, 4–6 µm deep pleats or folds with a density of 1–1.2 folds/µm of abdominal length. Straightening these folds can generate an approximately 6-fold length increase. The folds are already present beneath the female chalimus IV cuticle when the epidermis of this development stage starts to secrete the adult cuticle. Immediately before the final moult, the adult cuticle is super-folded with the whole cuticle displaying second-order folds, 8–10 µm deep.The capacity of Lernaeocera to engage in extensive cuticular modifications without recourse to a moult is compared with similar abilities shown by some insect species.     

Temperature influence on cohort parameters and demographic characteristics of the two cowpea coreids Clavigralla tomentosicollis and C. shadabi

Age-specific life tables of two important pests of cowpea, Vigna unguiculata (L.) Walp., the pod sucking bugs Clavigralla tomentosicollis Stål and C. shadabi Dolling (Heteroptera: Coreidae), were obtained from observations carried out at different temperatures. A biophysical model was found satisfactory to describe the temperature-response of developmental and mortality rates of egg and nymphal stages, with a peak developmental rate around 34°C in both species. The variability in development times was small and the experimental data did not permit any conclusion with regard to the Erlang probability density function. Survival of eggs and nymphs remained high between 20° and 30°C for both species. At temperatures above 34°C, C. tomentosicollis survivorship and fecundity was higher than that of C. shadabi, which in turn laid more eggs at temperatures between 20° and 30°C. Maximum fecundity is estimated to be at 29°C for C. tomentosicollis (99 eggs/female) and 26°C for C. shadabi (261 eggs/female). At 30°C, the intrinsic rate of increase reached a maximum in both species, 0.152 per day for C. tomentosicollis and 0.145 per day for C. shadabi, and remained high for C. tomentosicollis until 36°C. C. tomentosicollis performed significantly better on pigeonpea, Cajanus cajan Millsp., than on cowpea at higher temperatures.     

Temperature-dependent development and growth of Calanus sinicus (Copepoda: Calanoida) in the laboratory

The calanoid copepod Calanus sinicus was reared in the laboratory under excess food conditions, and its development and growth rates were measured at various temperatures. Egg development time (D_H, days) was dependent on temperature (T °C), and was expressed as D_H = 55.3 (T + 0.7)^–1.44. Post-embryonic development followed the equiproportional rule. The stage duration was short in NI and NII, but compensatingly longer in NIII. Between NIV and CII, it was nearly isochronal, and beyond CII, it tended to increase gradually. The time from egg to adult was expressed as D_CVI = 1258 (T + 0.7)^–1.44. The specific growth rate was also temperature-dependent and highest from CI to CIII, intermediate from NII to CI and from CIII to CV, and lowest from CV to CVI. The growth rates of C. sinicus are higher than those of co-occurring small copepods such as Paracalanus, Acartia and Microsetella.     

Spatial distribution of resting stages,rate of emergence from diapause and times to adulthood and to the appearance of the first clutch in 3 species of cyclopoid copepods

The spatial distribution of dormant copepodids of 3 species of cyclopoid copepods — Cyclops vicinus, Mesocyclops leuckarti and Thermocyclops crassus — was studied in 4 small lakes in South Germany. The rate of emergence from diapause and times from the resting stage to adulthood and from adulthood to the appearance of the first clutch was studied at 4 constant temperatures (5, 10, 15, 20 °C) in the laboratory. Resting stages of C. vicinus were always concentrated in the deepest parts of the lakes and were found relatively deep in the mud. M. leuckarti- and T. crassus-copepodids preferred shallow areas in deep lakes but were concentrated in the deep areas in shallow lakes. Copepodids of both species were always concentrated in the uppermost mud layers.Rate of emergence from diapause was strongly temperature-dependent. At high temperatures (20 °C) copepodids of all species under study emerged within 2 weeks. At lower temperatures C. vicinus copepodids showed the highest rate of emergence. At 5 to 10 °C only few M. leuckarti- and T. crassus-copepodids had emerged after the investigation period (7 weeks). Both C. vicinus and T. crassus showed the highest rate of emergence at the natural end of diapause but even at that time only few T. crassus-copepodids emerged at 5 °C. Times to adulthood at 5 °C were shortest in C. vicinus. At higher temperatures this species was passed by M. leuckarti. Times from adulthood to the appearance of the first clutch at 5–15 °C were shortest in C. vicinus. T. crassus produced no clutch at 5 and 10 °C.     

The life-cycle of the flatfish nematode Cucullanus heterochrous

Mature specimens of Cucullanus heterochrous Rudolphi, 1802 (Nematoda: Cucullanidae) were obtained from the intestine of the flounder, Platichthys flesus, from Danish waters. Eggs embryonate in seawater but do not hatch. Fully developed larvae pressed out of eggs are 430 microm long with amphids and dereids and enclosed within the cuticle of a previous larval stage. Infective larvae are believed to be in their third stage. Experimental studies showed that the polychaetes, Nereis spp., Scoloplos armiger, Brada villosa and Capitella sp., may act as intermediate hosts. In N. diversicolor the larvae increase their length to 1 mm within four weeks (15 degrees C) without moulting. Experimental infections showed that larvated eggs are not infective to fish, whereas >550 microm long larvae from polychaetes survived in 4-24 cm long flounders and plaice, Pleuronectes platessa. Third-stage larvae 550 microm to 1.1 mm long were found in the submucosa of the intestine one week post infection. At a length of about 800 microm to 1.4 mm they moult to fourth-stage larvae. Fourth-stage larvae, immature and mature worms occur in the intestine and rectum. Fourth-stage larvae and adults survived experimental transfer from one flounder to another. Similar developmental stages survived for two weeks in the intestine of experimentally infected cod, Gadus morhua.     

Effects of temperature on larval eclosion of the winter moth, Operophtera brumata

The developmental threshold and heat-unit requirements for larval eclosion of the winter moth, Operophtera brumata (L.) [Lepidoptera: Geometridae], were determined from experiments involving eggs exposed to various chilling and warming treatments. The developmental threshold was determined to be 4 °C. Eggs which were chilled below the developmental threshold required fewer heat-units for larval eclosion than did eggs not given a chill treatment. Eggs cultured at 14 °C required 470 (±47) degree-days for 50% larval eclosion. However, eggs chilled for 2 weeks at 1 °C and subsequently placed at 14 °C required 382 (±33) degree-days while eggs chilled for 12 weeks at 1 °C and subsequently placed at 14 °C required 156 (±12) degree-days. The results are discussed in relation to chilling intensity, diapause, and physiological-time models.

---

Résumé Le seuil de développement et la quantité de chaleur nécessaires pour l'éclosion larvaire chez Operophtera brumata (L.) (Lepidoptera: Geometridae) ont été déterminés en exposant les oeufs à différents régimes de refroidissement suivis de périodes de réchauffement. Le seuil de développement déterminé est de 4 °C. Les oeufs placés d'abord à des températures inférieures à celle du seuil de développement demandent moins de quantité de chaleur pour l'éclosion larvaire, que les oeufs qui n'ont pas été exposés à de basses températures. Les oeufs maintenus à 14 °C demandent 470 (±47) degrés-jours pour permettre 50% d'éclosion. Cependant, des oeufs maintenus pendant 2 semaines à 1 °C, puis à 14 °C, exigent 382 (±33) degrés-jours; ceux placés pendant 12 semaines à 1 °C, puis à 14 °C, en exigent 156 (±12). Les résultats sont discutés en relation avec l'intensité du refroidissement, la diapause et les modèles physiologico-temporels.

     

The effect of temperature on development and fecundityof Scymnus levaillanti

Development and fecundity of Scymnus levaillanti(Mulsant) were recorded at fiveconstant temperatures ranging from 15 to 35 ± 1 °C in 5 °C increments, 60 ± 5% RHand 16 h of artificial light (5000 Lux). Developmentaltime (egg to adult) of S. levaillantisignificantly decreased with increasing temperatures,ranging from 63.9 days at 15 °C to 11.1 days at35 °C. Development from egg to adult required305.2 DD above a developmental threshold estimated as11.7 °C. Oviposition periods lasted 86.5, 76.1,47.2, and 31.5 days at 20, 25, 30 and 35 °C,respectively. No eggs were deposited at 15 °C.Higher temperatures resulted in shorter generationtimes (T_O) and in decreased net reproductiverates (R_O) of the coccinellid. S.levaillanti kept at 30 °C produced 0.151females/female/day, the highest per capita rate ofpopulation growth (r_m). The `functional response'of larvae and adults of S. levaillanti matcheswell that described by Holling (1959) as Type 2.Daily number of eggs deposited by females increased toa plateau with increasing prey density. Resultsobtained here provide information about the biology ofS. levaillanti, and its feeding capacityindicates that it may act as an important control agent.     

Induction of diapausing amictic eggs in Synchaeta pectinata

Amictic females of a clone of S. pectinata from Star Lake (Norwich, Vermont) may produce diapausing as well as non-diapausing (subitaneous) eggs. The proportion of diapausing eggs produced in cultures was unaffected by temperature (12 vs 19 °C) or rotifer population density (minima of 0.33 vs 3 ind. ml^–1) at 19 °C. However, at 19 °C this proportion was higher in cultures maintained at a low food level suppressing reproduction (5 × 10³ cells ml^–1 Cryptomonas erosa) than in those maintained at a high food level (2 × 10⁴ cells ml^–1); the treatment effect was marginally significant (p=0.067). Consistent with the effect of low food availability, a period of starvation was very effective in inducing the development of diapausing eggs. None of 19 females cultured individually from hatching at 19 °C on C. erosa (2 × 10⁴ cells ml^–1) in 1-ml volumes produced any diapausing eggs in 4 days (0 out of 349 eggs), while 13 out of 16 females subjected to a 15-hour starvation period 6 hours after birth produced one or more diapausing eggs during that time (34% of the 158 eggs produced by the 16 females were diapausing). Diapausing eggs produced and left at 19 °C hatched after 4 to 13 days. Those produced in cultures with a low food level took significantly longer to hatch (9.7 days) than those produced in cultures with a high food level (8.1 days) (p=0.022). In natural communities, S. pectinata should be able to respond directly and rapidly to poor food conditions by producing eggs that undergo an obligatory dormant period before resuming development.     

Experimental studies on the life cycle ofJassa falcata (Crustacea,Amphipoda)

Jassa falcata (Leach), an unselective suspension feeder, was cultivated in standing, unaerated finger bowls, feeding on a mixture ofBrachionus plicatilis, Scrippsiella faeroense, Ulva spec., and natural detritus. This amphipod can also be maintained with diets composed of dead or live material of both plant and animal origin, but an addition of living zooplankton is necessary for longterm cultivation. Starvation resistance is higher in females than in males, and it is increased by lower temperatures. The life span ofJ. falcata increases with decreasing temperature, and it is generally higher in females (maximum: 252 days at 10°C) than in males. In laboratory culture, a bimodal mortality pattern is typical with high juvenile death rates, low mortality during the reproductive phase, and again increasingly high death rates toward the end of the life cycle. Growth rate depends on temperature, sex, and individual age. The temperature dependence of growth is particularly high in males, and it is higher in adults than in juveniles. The total number of moults is lower in males (5 to 6) than in females (7 to 9). Sexual maturity is attained at moult IV to V. The average incubation time of eggs is about 9 to 16 days (highest value at 10°C). Three to 4 broods were observed, with largest numbers of offspring at 10°C.     

Temperature influence on life table statistics of the chicken miteDermanyssus gallinae (Acari: Dermanyssidae)

An age-specific life table for the chicken miteDermanyssus gallinae (DeGeer, 1778) was based on various observations carried out at 25°C. The generation time was calculated to be 16.8 days; the intrinsic rate of natural increase was 0.12 per day, and the net reproductive rate was 7.2. A nonlinear function was found satisfactory to describe the developmental rate of the different immature lifestages at temperatures below 40°C. The stage-specific survival of the immature life-stages was generally high between 10 and 37°C, but decreased quickly outside this temperature range. Most of the eggs were laid during the first three weeks of the adult life. The proportion of surviving females rapidly decreases after moulting to the adult stage. At a temperature of 30°C, the highest number of eggs (3 eggs per day) was laid.     

A method for hatching the eggs of the aphid Schizaphis graminum

Techniques are described for the collection of fertile eggs of Schizaphis graminum (Rond.) on filter paper, and for the subsequent sterilization and incubation of the eggs under various temperature and photoperiodic conditions.19% of the eggs incubated continuously at 16°C in complete darkness hatched in 81 days after deposition. 45% of the eggs chilled at 6°C for 40 days (starting 10 days after deposition) hatched in 71 days if the postchilling incubation at 16°C was completed in darkness. The results indicate a further enhancement in the percentage egg hatch and a reduction in developmental time when the eggs were subjected to a light-dark regime during the post-chilling incubation.

---

Zusammenfassung Es wird eine einfache und effektive Methode beschrieben, die Eier von Schizaphis graminum auf Filterpapier zu sammeln, sie nachfolgend zu sterilisieren und unter verschiedenen Temperatur- und Photoperiodebedingungen bis zum Schlüpfen zu inkubieren.Hierbei wurden folgende Resulate erzielt: (a) Inkubation der Eier in vollkommener Dunkelheit bei 16°C führte zu einem Schlupferfolg von 19% nach einer Entwicklungszeit von im Mittel 81 Tagen; (b) Kühlung der Eier bei 6°C während 40 Tagen (vom 10. Tag nach der Eiablage an) erhöhte die Schlupfrate unter ansonsten gleichen Bedingungen auf 45% und reduzierte die Entwicklungszeit auf 71 Tage; (c) durch einen Licht/Dunkel-Rhythmus, dem die Eier nach der 40-tägigen Kühlung ausgesetzt wurden, konnte eine weitere Steigerung der Schlupfrate und eine Verkürzung der Entwicklungszeit erreicht werden.

     

The effect of temperature and water quality on the in vitro development and survival of Asellus aquaticus (Crustacea: Isopoda) eggs

The rate of development and degree of survival of Asellus aquaticus eggs outside the marsupium of ovigerous females are affected by water quality and temperature. Eggs were maintained in polluted river water and relatively clean canal water. Developmental rates increase with increased temperature, but survival decreases. Eggs from polluted site ovigerous females survive better in clean water than in polluted water. Eggs from clean site ovigerous females maintained in polluted water have significantly lower survival rates than eggs from the polluted site at all temperatures tested. The developmental rate of clean site eggs is increased significantly in polluted water at 10–25 °C, possibly as a response to the stress imposed upon them.It is suggested that the method outlined might form the basis of a useful bioassay technique for measuring water quality.     

Feeding, defecation, and development times of Meccus longipennis Usinger, 1939 (Hemiptera: Reduviidae: Triatominae) under laboratory conditions

Aspects related to hatching, time-lapse between presenting the blood-meal and beginning of feeding, feeding time, postfeed defecation delay, mortality, and fecundity for each stage of Meccus longipennis life-cycle were evaluated. The bugs were maintained in a dark incubator at 27 1 C and 80 5% rh, were fed weekly and checked daily for ecdysis or death. The hatching rate observed for 300 eggs was 76.7% and the average time of hatching was 19.8 days. Mean time-lapse between presentation of the blood meal and the beginning of feeding was under 5 min in nymphal stages and postfeed defecation delay was under 10 min in most stages, except in fourth and fifth stages. Mean feeding time was longer than 10 min in most stages, except in fourth stage. One hundred thirty-one nymphs (N) (65.5%) completed the cycle and the average time from NI to adult was 192.6 34.8 days. The average span in days for each stage was 18.1 for NI, 21.4 for NII, 29.5 for NIII, 45.5 for NIV and 55.9 for NV. The number of bloodmeals at each nymphal stage varied from 1 to 5. The mortality rate was 3.29 for NI, 6.8 for NII, 2.92 for NIII 3.76 for NIV, and 10.16 for NV nymphs. The average number of eggs laid per female in a 9-month period was 615.6. Based on our results, we conclude that M. longipennis has some biological and behavioral characteristics which influence its capacity of becoming infected and transmitting Trypanosoma cruzi to human populations in those areas of Mexico where it is currently present.     

Distinct effects of different low temperatures on the induction of NAD-sorbitol dehydrogenase activity in diapause eggs of the silkworm,Bombyx mori

Summary Diapause eggs of the silkworm, Bombyx mori, exposed to 5°C and 0.5°C from 2 or 30 days after oviposition, were examined for changes in contents of glycogen, sorbitol and glycerol. Cold acclimation did not alter the profile of accumulation of sorbitol from that in eggs kept continuously at 25°C. However, acclimation at 5°C resulted in conversion of sorbitol to glycogen, while acclimation at 0.5°C was not accompanied by the utilization of sorbitol. NAD-sorbitol dehydrogenase (NAD-SDH; EC 1.1.1.14) activity was examined in the cold-acclimated eggs. The activity was induced by acclimation at 5°C but not at 0.5°C. Incubation at 0.5°C suppressed any further increase in the activity that had been induced. Temperature-directed changes in NAD-SDH activity paralleled those in sorbitol content. Hatching of the diapause eggs was monitored after cold acclimation for various periods of time and subsequent transfer to 25°C. Incubation at 0.5°C was less effective than 5°C at breaking diapause. The time required for the eggs to hatch in synchrony after acclimation at 5°C coincided with that required for the induction of NAD-SDH activity. These results show that different effects result from acclimation at 5°C and near 0°C with respect to the control of NAD-SDH activity, that utilization of sorbitol is controlled by NAD-SDH activity, and that induction of this activity is temperature-dependent. Furthermore, induction of NAD-SDH activity is involved in the termination of diapause in B. mori.Abbreviations DH diapause hormone - NAD nicotinamide-adenine-dinucleotide - NAD-SDH NAD-sorbitol-dehydrogenase     

Demographic analyses of organophosphate-resistant and susceptible strains of greenhouse whitefly, Trialeurodes vaporariorum, on three cotton cultivars

Laboratory experiments were conducted using organophosphate-resistant and susceptible strains of greenhouse whitefly, Trialeurodes vaporariorum Westwood, to assess age-specific vital rates in individually-held adults, and development and survival in preadults on three cotton cultivars at 27±1 °C, 50±10% RH, and a photoperiod of 16:8 (L:D). Female whiteflies lived longer than males, with a maximum life expectancy of 29 days. Heaviest egg laying occurred at ages between 7 and 18 days when individual whiteflies laid > 10 eggs/day. Greenhouse whitefly populations doubled weekly, with stable age distribution of 63% eggs, 28% larvae, 5% pupae, and 4% adults. Analysis of various life history parameters that combine aspects of survival, developmental rates, and fecundity indicated no consistent differences in reproductive fitness between the two greenhouse whitefly strains. Of the three cotton cultivars tested, Pima S-6 was most susceptible, Acala SJ-2 was intermediate and Gumbo 500 was most resistant to greenhouse whitefly. Resistance of Gumbo 500 was expressed as slower developmental rates, reduced survival to adulthood, lower reproductive rates, and lower intrinsic rate of increase.     

Effect of acute pH depression on the survival of the freshwater amphipod Hyalella azteca at variable temperatures: field and laboratory studies

Field observations on temperature and pH of a small pond showed that a amphipod population of Hyalella azteca was exposed to variable seasonal pH between 5.10–5.85, and water temperatures between 2–21 °C. Laboratory experiments were designed to simulate seasonal temperatures and field pHs of a small pond habitat. Laboratory bioassay experiments were conducted to determine the survival of Hyalella azteca at pHs 4, 5, 6 and 7, and varying temperatures of 5°, 10°, 15°, 20° and 25 °C.The LT₁₀₀ at pH 4 and 25 °C was 5.7 ± 0.47 days, compared to 47.3 ± 2.49 days at 5 °C. An Analysis of Variance (ANOVA) showed temperature was a significant (p > 0.0001) source of variation in the acute lethality of pH to H. azteca. A Duncans Multiple Range Test (DMRT) further showed that in laboratory experiments at pH 4, there was a significant difference ( = 0.01) between the LT_100s at 5°, 10°, 15° and 20 °C, but not between temperatures 20° and 25 °C.     

Biological control of strawberry tarsonemid mite Phytonemus pallidus and two-spotted spider mite Tetranychus urticae on strawberry in the UK using species of Neoseiulus (Amblyseius) (Acari: Phytoseiidae)

Two species of Neoseiulus, N. californicus and N. cucumeris, showed potential for biocontrol of phytophagous mites on strawberry. N. californicus controlled Tetranychus urticae on potted strawberry plants in a gauze-sided glasshouse at temperatures comparableto early summer in the UK (8–20°C). Both species of phytoseiid reducednumbers of the tarsonemid Phytonemus pallidus on potted strawberry plants under glasshouse conditions (15–23°C). In several experiments reductions in the range of 71–81% in numbers of tarsonemid active stages and eggs, compared to non-release plants, were obtained. The importance of establishing a suitable predator: prey ratio at an earlystage was demonstrated in an experiment where an initial ratio of 1 N. cucumeris: 10 P. pallidus gave a greater degree of controlthan 1:20 or 1:40.     

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.