Zur fortpflanzungsbiologie von mesostoma ehrenbergii (Focke, 1836) (Turbellaria)

1. At temperature levels from 10 to 25°C animals from resting eggs produce subitaneous eggs independent on temperature. In contrast animals from subitaneous eggs produce subitaneous eggs dependent on temperature. At a high rate subitaneous eggs are only formed at temperature levels above 20°C.
2. Below 10°C no development occurs in the juveniles. At temperatures of 30/22°C (24.7°C) the first subitaneous eggs are formed after 6–9 days, at 14/9°C (10.7°C) they are formed after 34 days. At different temperature levels the developmental rate of the young is from 10.5 to 42 days. One generation extends over 16.5 (30/22°C) to 75 days (14/9°C). The average egg production is 10–20 subitaneous eggs or 30–60 resting eggs. The maximum egg production of one individual is 50 subitaneous eggs or 84 resting eggs. 50% of the animals have just formed resting eggs, before the juveniles are hatched. Resting eggs in the first egg-batch are formed 6–20 days later than subitaneous eggs. The duration of life is between 65 (30/22°C) and 140 days (19/13°C).
3. Young worms in resting eggs have a dormance period of at least 15–30 days.

At room temperatures (20°C) no juvenile in resting eggs hatches from water. By combining room and refrigerator (3.5°C) temperatures the hatching rate increases to a maximum of 85%. To reach a hatching rate of 50–65% the influence of low temperatures must be at least 30 days. At room temperatures 60% of the young in resting eggs hatch from mud covered with water. Combining high and low temperatures the hatching success is between 67 and 81%, where the highest percentage of the young may hatch at room temperature. Up to 90 days low temperatures cause a maximum hatching rate of 79%. It decreases to approximately 30% after 180 days. At high temperatures resting eggs preserved in 100% moist mud, survive for two months. By adding a period of low temperatures the hatching rate increases to a maximum of 52%. Low temperatures are survived for more than 6 months. Up to 30 days preservation at 3.5°C causes a maximum hatching rate of 61%, up to 12o days it decreases to 30%. At room temperature the young in resting eggs are not resistant against air-dried mud (30–40% rel. air moisture). Combining high and low temperatures air-dried mud is endured 1 month (hatching rate 5–14%). Preservation of 30–120 days at 3.5°C and 70% rel. air moisture result in a hatching rate of 43–61%. li]4. In the open air in Middle-Europe there occur 5–6 generations of M. ehrenbergii per life-cycle. The first generation hatches from resting eggs in May, where the production of subitaneous eggs is independent on temperature. All other generations up to October hatch from subitaneous eggs. The egg-production of those worms is dependent on environmental factors. In summer subitaneous egg production prevails, in autumn resting egg production. The abundance during the life-cycle is dependent on the number of animals which produce subitaneous eggs. Resting eggs are predestinated to endure periods of dryness and cold. The life-cycles of the species M. lingua and M. productum are different from those of M. ehrenbergii in length and in the number of generations. In both species 7 generations occur over 8 to 8.5 respectively 5.5 months. M. nigrirostrum only forms resting eggs. The life-cycle consists of one generation from February/March to May/June.     

Hatching of Daphnia sexual eggs. I. Intraspecific differences in the hatching responses of D. magna eggs

• 1 To test the hypothesis that the variability in hatching response of the sexual eggs of Daphnia has a genetic component, hatching after a standardized decapsulation technique was studied in different D. magna families, resulting from intra- as well as interclonal crosses.
• 2 There were significant differences in hatching response between families. Average hatching rates ranged from 0.0% to 81.9%, depending on the family under study.
• 3 Offspring-on-parent regressions indicate that the hatching rate-of sexual eggs is to a large extent determined by the genotype of the mother (maternal inheritance).
• 4 Our results suggest that there is ample generic variation on a microgeographic scale for characteristics related to hatching of sexual eggs in Daphnia.

     

Direct and transgenerational effects of an experimental heatwave on early life stages in a freshwater snail

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Variable egg development of Dinocras spp. (Plecoptera, Perlidae) and the stonefly seed bank theory

1. Temperature dependence of egg development of Dinocras cephalotes (Curtis) (three German and one Norwegian population) and Slovenian D. megacephala (Klapálek) was studied under a constant 14 : 10 light : dark photoperiod and constant temperature ranges of 4–24 °C and 4–18 °C, respectively. D. cephalotes was also incubated under seasonal field conditions; natural daylength and fluctuating temperatures had no modifying effect. 2. Both species have very similar lower threshold temperatures (4 and 3.5 °C, respectively), thermal demand for development (c. 600 degree days) and high dependence of mean incubation period on temperature (exponents of regressions near 1.5). Present data on D. cephalotes agree with the literature on British and Norwegian material of the same species. 3. Development occurs only at cue temperatures above the lower threshold. Cue temperatures range from 6 °C (some D. megacephala) to 14 °C (some D. cephalotes) and vary strongly within and between egg masses of D. cephalotes. Variation is not random, but seems to be genetically determined. 4. The variable temperature response renders study of effects of particular experimental regimes, and comparisons between local populations, difficult. 5. A latitudinal gradient in cue temperatures for development from 6 °C at c. 46 °N to 12 or even 14 °C at c. 61 °N seems to reflect reduced diversity at high latitudes. 6. Average success of spontaneous hatching exceeded 90% between 12 and 20 °C, but declined towards higher and lower temperatures. 7. Unhatched eggs were not dead but in parapause; development at other, higher or lower, temperatures was induced. Spontaneous plus induced hatching success approached 90%. Developing eggs rarely died; most dead eggs were apparently unfertilized. 8. Dormant plecopteran eggs are proposed to form a seed bank in stream bed sediments. Highly successful development after up to 220 days of dormancy was ascertained in Dinocras, and survival for up to 3 years is reported for other Perloidea. 9. Only systellognathan egg morphology provides options for long dormancy; the other plecopteran superfamilies, notably Nemouroidea, follow different strategies.     

Temperature effects on embryonic development of Paratlanticus ussuriensis (Orthoptera: Tettigoniidae) in relation to its prolonged diapause

Paratlanticus ussuriensis eggs overwinter by entering diapause, which can be prolonged to more than 1 year depending on environmental conditions. To determine temperature effects on diapause duration of P. ussuriensis eggs, the rates of embryonic development and hatching were compared at various temperatures conditions by measuring embryonic stages and egg weights. Most eggs stayed in a very young stage (blastoderm formation, stage 4) when reared at 15 and 20 °C, 10–30% eggs developed into middle or late stages when reared at 25 °C, and most embryos developed fully (stage 23/24) when reared at 30 °C. Egg weight at 30 °C was 1.5 times higher than those reared at 20 °C. Chilling induced hatching in embryos at stage 23/24. Chilling caused stage 4 embryos to develop into stage 24, but they failed to hatch in response to a second warm period. Thus, P. ussuriensis eggs can overwinter either as young embryos (initial diapause) or as fully-developed embryos (final diapause). Eggs that experience an initial diapause overwinter again the second year in a final stage diapause. The post-diapause period was shorter when embryos overwintered in a final stage diapause. The hatching rate was highest in a temperature range of 7.5–15 °C. Our results suggest that temperature is an important environmental factor for the control of prolonged diapause in P. ussuriensis and initial diapause plays an important role in the control of its life cycle.     

The transition from sitting on eggs to sitting on young in ring doves, Streptopelia risoria: squab-egg preferences during the normal cycle.

Ring doves of both sexes sit on young squabs after hatching in much the same manner as they sit on eggs before hatching, but this study demonstrates that the preferred stimulus varies with the state of the animal. A simultaneous, squab-egg choice test was given on days 1, 4, 10, and 13 of incubation and on the day following hatching in normal reproductive cycles of experienced and naïve male and female ring doves. Naïve doves were more likely than experienced doves to choose eggs throughout the cycle (P<0·005) and, overall, eggs were more likely to be chosen during early incubation and squabs posthatching (P<0·005).     

Biology of the Collembola Xenylla grisea Axelson and Lepidocyrtus cyaneus f. cinereus Folsom

• 1 Xenylla grisea Axelson and Lepidocyrtus cyaneus f. cinereus Folsom were reared on brown whole wheat flour in culture jars containing a base of plaster of paris and charcoal.
• 2 Sexes in X.grisea may be differentiated by the combination of three characters: length, colour and body shape. No parthenogenesis was observed in either species.
• 3 At room temperature (25–27°C), females of X.grisea began laying eggs after the fourth moult and required 10–15 days (mean of 12.6) to reach sexual maturity from the day of hatching. With L.cyaneus f. cinereus, average periods from hatching to maturity were 16.8, 27.4 and 43.2 days at temperatures of 26.5, 22 and 15°C, respectively.

     

Low temperature tolerance and starvation ability of the oak processionary moth: implications in a context of increasing epidemics

• 1 We investigated how modifications in winter and spring temperature conditions may affect the survival of a spring‐hatching Lepidoptera, the oak processionary moth Thaumetopoea processionea.
• 2 Supercooling and chilling injury experiments indicate that eggs are especially cold hardy at the start of the winter period, although this ability is reduced later in the season. In the spring, young larvae are sufficiently cold hardy to ensure no direct mortality as a result of late frosts.
• 3 A comparison of phenological models shows that neonate larvae may await the unfolding of new oak leaves for relatively long periods (e.g. 1–30 days). Under both low (4°C after 5 days at 16°C) and high temperature experimental scenarios (constant 16°C), the majority of neonate larvae can survive starvation for more than 2 weeks.
• 4 Larvae may also suffer from food depletion once their development has been initiated (e.g. during cold springs) if the threshold temperature for feeding is not reached for several consecutive days, or in the case of late frosts affecting foliage availability. When temperature is reduced to 4°C, developing larvae become inactive and do not feed anymore; their starvation survival capability is reduced to approximately 2 weeks (cold spring hypothesis). At 16°C, developing larvae that are deprived of food can only survive for 10 days (late frost hypothesis).
• 5 We conclude that, in the oak processionary moth, neonate larvae are relatively well adapted to early hatching relative to budburst, ensuring them the highest foliage quality for development. In some years, however, phenological asynchrony or cold spring conditions may affect the persistence of populations at the limits of the species' range.

     

Delayed Egg Hatching and Semivoltinism in the Nearctic Stonefly Megarcys signata (Plecoptera: Perlodidae)

Delayed egg hatching can influence the survival of aquatic insects by reducing exposure to competitors, predators, parasites, or unfavorable environmental conditions. We examined egg development in a Colorado population of the stonefly, Megarcys signata (Plecoptera: Perlodidae), whose larvae inhabit high altitude streams in the Rocky Mountains of western North America. Five-thousand fertilized eggs were collected from 40 different females and incubated in the East River, Gunnison County, Colorado, until late fall, at which time unhatched eggs were transported to incubation chambers in Ithaca, New York. We used three different combinations of photoperiod and temperature (10L:14D, 4°C; 10L:14D, 8°C; 8L:16D, 8°C) in an attempt to induce hatching. Eggs in the treatments with temperatures elevated above normal winter temperatures in the East River (8°C) began developing after 6 months, whereas eggs in the treatment most closely simulating natural stream conditions (4°C) did not hatch after 10 months of incubation. Our data indicate that this population of Megarcys signata has an extended egg stage that persists for almost a year, and that it is semivoltine at these elevations of 2885 and 2895 meters.     

Influence of temperature on hatching of winter eggs of fruit-tree red spider mite, Panonychus ulmi (Koch)

The effects of the duration and degree of chilling, and the temperature of incubation, on hatching of winter eggs of Panonychus ulmi (Koch) were investigated. For chilling, 0°C and 5°C were more effective than — 5° and 9°, and the limits for the reaction were close to — 10° and 15°. As the chilling period was increased from 60 to 200 days, the percentage hatch on incubation at 21° increased, and the mean incubation time and its variance decreased. Before the maximum effect of chilling was achieved, percentage hatch on incubation at 9° and 15° was higher than at 21°; 27° was lethal to most winter eggs though not to summer eggs. After chilling, the later stages of diapause development could occur at temperatures from 0° to 21°₎ i.e. above and below the threshold temperature for morphogenesis, 6–7° in both winter and summer eggs. Diapause development cannot, therefore, be a unitary process. The significance of the results is discussed in relation to forecasting the time of hatch in the field, and to the phenological aspects of hatching in the spring.     

Comparison of egg period, hatching rate, and first-instar nymphs among three species of stonefly

Egg period was compared among several temperature conditions (11°C, 16°C, 20°C, 23°C) in Sweltsa sp., Stavsolus japonicus, and Isoperla aizuana (Plecoptera). The shortest mean egg incubation period was 27.8 days at 20°C in Sweltsa sp., 118.1 days at 16°C in Stavsolus japonicus, and 162.0 days at 20°C in Isoperla aizuana on average. Egg hatching rate was also the highest at the water temperature that provided the shortest egg incubation period. Based on laboratory data, eggs of Sweltsa sp. were considered to be deposited in May and hatched in June in the field. Thus, they must have spent the summer as nymphs in the field. Eggs of Stavsolus japonicus and Isoperla aizuana were considered to be deposited in April to May and hatched in September to October in the field. Visible eyes of Stavsolus japonicus and Isoperla aizuana appeared in August. It is likely that the long egg period of Stavsolus japonicus and Isoperla aizuana reflects that these two species spend the summer as dormant eggs in the field.     

THE EFFECT OF CONSTANT TEMPERATURES ON THE HATCHING OF EGGS AND SURVIVAL OF THE FRESHWATER SNAIL BIOMPHALARIA GLABRATA (SAY)

SUMMARY

The incubation period and percentage hatching of eggs of pigmented and unpigmented Biomphalaria glabrata at constant temperatures were investigated in the range 14 °C to 34 °C. In order to determine the influence of extreme temperatures on adult snails, specimens of the same species were exposed to 0 °C and 40 °C for selected time periods. The results indicate that sustained temperatures below 16 °C and above 32 °C are detrimental to the development and hatching of B. glabrata embryos. The optimum temperatures for incubation period and hatching differ from each other. As far as temperature is concerned, this foreign snail species should be capable of successfully colonizing the warmer parts of southern Africa.     

How incubation temperature influences the physiology and growth of embryonic lizards

Eggs of two small Australian lizards, Lampropholis guichenoti and Bassiana duperreyi, were incubated to hatching at 25 °C and 30 °C. Incubation periods were significantly longer at 25 °C in both species, and temperature had a greater effect on the incubation period of B. duperreyi (41.0 days at 25 °C; 23.1 days at 30 °C) than L. guichenoti (40.1 days at 25 °C; 27.7 days at 30 °C). Patterns of oxygen consumption were similar in both species at both temperatures, being sigmoidal in shape with a fall in the rate of oxygen consumption just prior to hatching. The higher incubation temperature resulted in higher peak and higher pre-hatch rates of oxygen consumption in both species. Total amount of oxygen consumed during incubation was independent of temperature in B. duperreyi, in which approximately 50 ml oxygen was consumed at both temperatures, but eggs of L. guichenoti incubated at 30 °C consumed significantly more (32.6 ml) than eggs incubated at 25 °C (28.5 ml). Hatchling mass was unaffected by either incubation temperature or the amount of water absorbed by eggs during incubation in both species. The energetic production cost of hatchling B. duperreyi (3.52 kJ · g⁻¹) was independent of incubation temperature, whereas in L. guichenoti the production cost was greater at 30 °C (4.00 kJ · g⁻¹) than at 25 °C (3.47 kJ · g⁻¹). Snout-vent lengths and mass of hatchlings were unaffected by incubation temperature in both species, but hatchling B. duperreyi incubated at 30 °C had longer tails (29.3 mm) than those from eggs incubated at 25 °C (26.2 mm). These results indicate that incubation temperature can affect the quality of hatchling lizards in terms of embryonic energy consumption and hatchling morphology. Accepted: 27 January 2000     

Artificial incubation of California condor Gymnogyps californianus eggs removed from the wild

The currrent California condor (Gymnogyps californianus) recovery plan entails increasing the reproductive rate via replacement-clutch manipulation of eggs. During the period from 1983 to 1985, 15 eggs were removed from wild nesting pairs for artificial incubation. The eggs were incubated at a dry bulb temperature of 36.4°C in modified forced-air Lyon Electric incubators. The incubation humidity was adjusted for individual eggs based on weight loss data (water = weight), 25.6–30.0°C wet bulb (41.0–63.0% Relative Humidity (RH)). The chicks were hatched initially under forced-air conditions of 36.1°C dry bulb, 31.1–01.7°C wet bulb (70.0–73.0% RH). In 1984, hatching parameters were changed to still-air conditions, 36.1°C dry bulb (top of the egg), 35.0°C dry bulb (bottom of the egg), 31.1–31.7°C wet bulb (70.0-73.0% RH). Tactile and auditory stimulation was utilized during the pip-to-hatch interval. From among 15 eggs collected, 13 hatched, and 12 condor chicks were raised successfully (hatchability: 86.7%; survivability: 92.3%).     

In situ Development of Perch Eggs,Perca fluviutilis L. (Pisces,Percidae) in a Small Eutrophic Lake,Lake Plussee,Holstein, Germany

Naturally spawned egg strands of perch, Perca fluviatilis L. were sampled from exposed fir trees submerged in Lake Plußsee, Holstein, Northern Germany from April to May 1989. These were incubated in situ and in the laboratory to estimate the viability, development and abnormalities of the embryos. From the in siru incubated eggs 91.6% embryos were viable, the nonviable portion comprising 1.1 % unfertilized eggs, 5.1 % dead and 2.2 % with abnormalities. As compared to the eggs incubated in the laboratory with 84.1 % viable embryos, the nonviable portion consisting 1.1 % unfertilized eggs, 11.3 % dead and 3.5 % with abnormalities. Incubation rate of P. fluviatilis embryos both in situ and laboratory, ranged from 200-210 ATUs (10°C in situ and 8°C in the laboratory) with incubation period of 20-27 days from fertilization to 50 % hatching.     

Environmental factors affecting hatching of rotifer (Brachionus plicatilis) resting eggs

Hatching experiments were carried out on a population of Brachionus plicatilis (Dor strain) resting eggs produced in batch laboratory cultures under controlled conditions and then stored for at least one month at 4 °C in the dark. Light was found to be obligatory for termination of dormancy. Over the temperature range of 10–30 °C (at 9.0‰ salinity), hatching was optimal (40–70%) at 10–15 °C and decreased linearly with the rise in incubation temperature. Resting eggs incubated over a salinity range of 9–40‰ (at 15 °C) showed optimal hatching at 16‰. Incubation of resting eggs in distilled water permitted normal embryonic development, but neonates died at eclosion. Presence of algae, Chlorella stigmatophora (0.5 × 10⁶ cell ml^?1), was found to aid hatching.     

To hatch or not to hatch? Egg hatch response to larval density and to larval contact in a treehole mosquito

Abstract.

• 1 We investigated the effect on egg hatch of exposure to: (1) varying larval density, and (2) larval contact in Aedes triseriatus Say (Diptera: Culicidae). For 2 days in the laboratory we submerged eggs into a treehole water medium containing 0 (control), 4, 12 or 24 larvae that could either contact the eggs directly or were separated from them by a screen. Following treatment, abundance of microorganisms on the egg surfaces, a food source for newly hatched larvae and a proposed hatching stimulus, was assessed by counts made from serial dilutions of samples.
• 2 We discovered a complex hatching response to larval contact and to larval density, and an interaction between these two factors in their effect on microbial growth. Hatching was inhibited in the 0-larva control, even though microorganisms grew abundantly on the eggs. Hatch rate, as well as microbial counts, were high for eggs in direct contact with 4 larvae. As density increased in the larval contact treatment, microorganisms disappeared from the egg surfaces and hatch rate declined.
• 3 When protected from larval grazing, eggs supported numerous microbial colonies irrespective of larval density. In contrast to the contact treatment group, egg hatch increased with increasing larval density. These observations suggest that the combination of microbial growth and a larval factor stimulates hatch. This hatching response may have evolved because both abundant microorganisms and numerous larvae reflect a habitat of good quality.

     

Effects of low temperatures on NAD-sorbitol dehydrogenase activity and morphogenesis in non-diapause eggs of the silkworm,Bombyx mori

• 1.1. The activity of NAD-sorbitol dehydrogenase (NAD-SDH; EC 1.1.1.14) and levels of sorbitol were examined in non-diapause eggs of the silkworm, Bombyx mori, exposed to temperatures of 20-0.5°C from 1 day after oviposition. The morphology of embryos in the cold-acclimated eggs and the hatching of eggs after transfer to 25°C were monitored.
• 2.2. Temperatures between 15 and 0.5°C retarded the development of NAD-SDH activity at a specific embryonic stage that was comparable to diapause, and sorbitol accumulated in the eggs.
• 3.3. With the appearance of NAD-SDH activity, sorbitol was converted into glycogen, just as it is in diapause eggs. The results indicate that NAD-SDH participates in the utilization of sorbitol rather than in its formation in non-diapause eggs.
• 4.4. Distinct effects of low temperatures on the morphological development of the embryos are also discussed.

     

Effects of down collection on incubation temperature, nesting behaviour and hatching success of common eiders (Somateria mollissima) in west Iceland

Incubating common eiders (Somateria mollissima) insulate their nests with down to maintain desirable heat and humidity for their eggs. Eiderdown has been collected by Icelandic farmers for centuries, and down is replaced by hay during collection. This study determined whether down collecting affected the female eiders or their hatching success. We compared the following variables between down and hay nests: incubation temperature in the nest, incubation constancy, recess frequency, recess duration, egg rotation and hatching success of the clutch. Temperature data loggers recorded nest temperatures from 3 June to 9 July 2006 in nests insulated with down (n = 12) and hay (n = 12). The mean incubation temperatures, 31.5 and 30.7°C, in down and hay nests, or the maximum and minimum temperatures, did not differ between nest types where hatching succeeded. Cooling rates in down, on average 0.34°C/min and hay nests 0.44°C/min, were similar during incubation recesses. Females left their nests 0–4 times every 24 h regardless of nest type, for a mean duration of 45 and 47.5 min in down and hay nests, respectively. The mean frequency of egg rotation, 13.9 and 15.3 times every 24 h, was similar between down and hay nests, respectively. Hatching success adjusted for clutch size was similar, 0.60 and 0.67 in down and hay nests. These findings indicate that nest down is not a critical factor for the incubating eider. Because of high effect sizes for cooling rate and hatching success, we hesitate to conclude that absolutely no effects exist. However, we conclude that delaying down collection until just before eggs hatch will minimize any possible effect of down collection on females.     

Temperature‐dependent development of the double‐spined spruce bark beetle Ips duplicatus (Sahlberg, 1836) (Coleoptera; Curculionidae)

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