Field and laboratory studies on the effects of temperature on the development of the carrot fly (Psila rosae F.)

The thermal requirements for the pre-oviposition period, egg, larval, pupal and adult stages of the carrot fly were measured under field conditions and at a range of constant temperatures in the laboratory. In the laboratory, the pre-oviposition period lasted from 4 days at 24^oC to 28 days at 9^oC. In general, female carrot flies laid about 20–40 eggs in each batch. Once the first eggs had been laid, subsequent batches were laid after an average of 3 days at 24^oC to 7 days at 11.5^oC. The numbers of days required for egg, larval and pupal development ranged from 5, 31 and 24 days respectively at 21.5^oC to 25, 145 and 84 days respectively at 9^oC. Under laboratory conditions, complete development from egg to adult required from 60 days at 21.5^oC to 254 days at 9^oC. Newly-formed carrot fly pupae were exposed to temperatures of 22–30^oC for various 5–10 day periods during pupal development. Exposure to temperatures of 24^oC and 26^oC caused some, and exposure to 28^oC and 30^oC caused all, of the pupae to delay development. Pupae were sensitive to high temperatures only for approximately 4–10 days after pupation. Under field conditions between mid-May and early September, full carrot fly development (egg-adult) took 84–100 days. The numbers of day-degrees required (base temperatures of 2^oC and 4^oC) for carrot fly development in the laboratory and in the field were similar for egg hatching but not for the pre-oviposition period or for egg-adult development. The thermal requirement for fly development in the field varied between inoculation dates, fewest day-degrees being required when development was rapid.     

The biology of the West African bush-cricket,Euthypoda acutipennis Karsch (Orthoptera: Tettigoniidae)

This paper presents the results of the first comprehensive study of the biology of a tropical bush-cricket. The eggs were laid without any external protective structures and lost water readily in unsaturated air; losses of more than 16% of the original fresh weight were usually fatal. Development and hatching took place only if the eggs were in contact with water. The water content increased by about 500% during development. The mean incubation period was 171 and 116 days at constant temperatures of 20^oC and 28^oC, respectively, but at temperatures fluctuating by±3°C about a mean of 28°C this period was reduced to a mean of 88 days. The eggs failed to develop if exposed to freezing temperatures for more than five days or kept at a constant temperature of 307deg;C or above. The duration of the nymphal period varied from 83 to 131 days at a temperature range of 22–30°C (mean 26° C). There were four or five nymphal instars in the male and five or six in the female. The linear growth of the hind femur conformed to Dyar's law. There was a conspicuous colour change during development, all the first-instar nymphs being leaf green and the adults predominantly brown. In nature the species lives exclusively on the forest floor and is markedly nocturnal in habits, hiding underneath litter during the day. The eggs are dormant during the dry season, hatching at the onset of the rains (March/April at Ibadan). The nymphs reach maturity from July onwards and the adults have mostly died off by the end of the rainy season (October). In the laboratory the species was found to have a temperature preference of 26–32°C, immobilization setting in at 18°C and 42°C, and a humidity preference of 60–80% R.H.; this corresponds with the prevailing conditions in its forest habitat. The nocturnal pattern of activity persisted for several days in continuous darkness, with no marked acceleration. Movement was inhibited for several days by artificial illumination. Reversed illumination reversed the rhythm of activity.     

Effect of fluctuating temperature on the duration of embryonic development in two Ecdyonurus spp. and Rhithrogena cf. hybrida (Ephemeroptera) from Austrian streams

Summary Eggs of Ecdyonurus picteti from the Herrnalmbach and Seebach, and E. venosus and Rhithrogena cf. hybrida from the Seebach were fertilized artificially and kept at fluctuating temperatures (range 2.8°–18.1° C) in the laboratory. The percentage of eggs that hatched at each sinusoidal temperature cycle ranged from 0 to 49% and values were similar to those obtained for eggs reared under constant temperature conditions. The hatching time (days after fertilization for 10, 50% and 90% of the eggs to hatch) decreased with increasing temperature and the relationship between the two variables was well described by a powerlaw within the range 2.8°–18.1° C for E. venosus. A similar relationship has been found for the effect of constant temperature on the hatching time of eggs of E. venosus. It appears that the effect of temperature on the rate of change in the hatching time and the rate of development is approximately similar for both constant and fluctuating temperatures.     

Development times and fecundity of three important arthropod pests of strawberry in the United Kingdom

The development rates and fecundity of three important pests of strawberry in the UK were determined over a range of temperatures. Development time of the strawberry tarsonemid mite, Phytonemus pallidus, from egg lay to adult, ranged from a mean of 28.4 days at 12.5°C to 8.8 days at 25°C. No nymphs developed to adult at 10°C. Females lived for up to 45 days and laid a mean of 24.3 and 28.5 eggs at 20°C and 25°C respectively. Total development time from egg lay to adult for the strawberry blossom weevil, Anthonomus rubi, ranged from a mean of 95.7 days at 10°C to 18.2 days at 25°C. Mean fecundity at 20°C was 157.6 eggs, and the oviposition period averaged 71.6 days. When nymphs were reared on strawberry, development of the European tarnished plant bug, Lygus rugulipennis, from egg lay to adult, ranged from 83.8 days at 15°C to 28.8 days at 25°C. Development times on groundsel were shorter and ranged from 65.6 to 22.2 days at 15°C and 25°C. Only two nymphs developed to adults at 10°C; no eggs hatched at that temperature. Mean fecundity at 20°C was 75.4 eggs, but ranged from 23 to 179. Under a fluctuating temperature regime of 10°C for 12 h:20°C for 12 h, nymphs of L. rugulipennis took 40.3 days to become adult on strawberry, and 33.4 days on groundsel. Simple linear models fitted the developmental rate ‐ constant temperature relationship well for all species, accounting for 95–98% of the total variation in observed developmental rates. Development under fluctuating temperatures illustrated the potential problem of extrapolating linear models beyond the conditions of the experiment.     

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.     

Effect of temperature on reproduction and embryonic development of the cabbage stem flea beetle,Psylliodes chrysocephala L., (Coleoptera: Chrysomelidae)

The cabbage stem flea beetle, Psylliodes chrysocephala (L.) (Coleoptera: Chrysomelidae), is a major pest of winter oilseed rape. Despite the importance of this pest, detailed information on reproduction to predict risk of crop damage is lacking. This study investigates the effect of temperature on parameters of reproduction, egg development and viability at five constant temperatures. Significant temperature effects were found on the pre‐oviposition period, total number of eggs laid, daily oviposition rate, female longevity, egg‐development rate and viability. The mean length of the pre‐oviposition period ranged from 93.1 days at 4°C to 14.6 days at 20°C. Analysis of total number of eggs laid and daily oviposition rate during female lifespan estimated the highest total number of eggs laid (696 eggs/female) at 16°C and the highest oviposition rate (6.8 eggs/female and day) at 20°C. The daily oviposition rate at 20°C was not significantly higher than 5.4 eggs/female and day at 16°C. Female longevity was significantly longer at 4°C, shorter at 20°C and not significantly different between 8, 12 and 16°C. Estimated 50% survival time of females was 239, 153, 195, 186 and 78 days at 4, 8, 12, 16 and 20°C, respectively. A linear model of egg development at 8–20°C estimated the lower developmental threshold to be 5.1°C and the thermal constant for development 184.9 degree‐days. The percentage of eggs hatching was significantly lower at 4°C than at all other temperatures tested. The estimated mean hatching percentages were 47.3%, 70.0%, 72.4%, 66.2% and 67.9% at 4, 8, 12, 16 and 20°C, respectively. These results can be used to predict the start and intensity of egg‐laying in the autumn and the appearance of larvae in the field from knowledge about time of field invasion and from monitoring the weather.     

Adaptive difference in daily timing of hatch in two locust species,Schistocerca gregaria and Locusta migratoria: The effects of thermocycles and phase polyphenism

This study examined the effects of temperature and phase polyphenism on egg hatching time in the desert locust, Schistocerca gregaria, and the migratory locust, Locusta migratoria. The two species exhibited differences and similarities in hatching behavior when exposed to different temperature conditions. In 12-h thermocycles of various temperatures, the S. gregaria eggs hatched during the cryoperiod (low temperature period), whereas L. migratoria eggs hatched during the thermoperiod (high temperature period). The eggs of both species hatched during the species-specific period of the thermoperiod in response to a temperature difference as small as 1 °C. Furthermore, the locusts adjusted hatching time to a new thermal environment that occurred shortly before the expected hatching time. In both species, the hatching of the eggs was synchronized to a specific time of the day, and two hatching peaks separated by approximately 1 day were observed at a constant temperature after the eggs were transferred from thermocycles 3 days before hatching. Eggs laid by gregarious females hatched earlier than those laid by solitarious females in S. gregaria but this difference was not observed in L. migratoria.     

Hatching from cysts and egg sacs of Heterodera cruciferae and effects of temperature on hatching and development on oilseed rape

Juveniles hatched readily from field cysts and very readily from eggs in egg sacs of Heterodera cruciferae, when exposed to oilseed rape root diffusate. They hatched very poorly, however, from white or brown females from which the above egg sacs had been removed. Some hatching occurred at 8 ^oC but much more occurred at 12 , 16, 20 and 24 ^oC, with most at 16 ^oC. Development of juveniles in roots of oilseed rape occurred throughout the range 8–24 ^oC, and proceeded faster the higher the temperature. The basal development temperature was taken as 5 ^oC and the number of day degrees above this temperature required to reach each stage of development was calculated. From invasion of roots to the hatching of F₁ juveniles required an average of 680 day degrees, but only 210 day degrees were required for the first appearance of egg sacs on adult females. On this basis, two consecutive generations of H, cruciferae would be possible on autumn-sown oilseed rape in southern England, but the second would mature fully only after the crop was harvested. In Scotland, two consecutive generations could also occur but the second would be much less mature by harvest: only about 850 day degrees are available compared to almost 1100 in southern England. In practice, however, overlapping generations probably occur due to flushes of hatching of juveniles (i) at sowing, (ii) when soils warm up after winter and (iii) when the first generation completes its development. The proportion of eggs found in egg sacs was never more than 37% and some field cysts contained about 220 eggs; their egg sacs may, therefore, have contained as many as 150 eggs. Any study of population dynamics or damage assessment will require a quantification of the contribution of eggs in egg sacs to population density. Oilseed rape is direct drilled and may, therefore, be more sensitive to a given population density of the nematode than host crops which are transplanted.     

Effect of temperature on the hatching time of eggs of Ephemerella ignita (Poda) (Ephemeroptera:Ephemerellidae)

SUMMARY. Eggs of Ephemerella ignita (Poda) were kept at eight constant temperatures (range 5.9–19.8°C) in the laboratory. Over 85% of the eggs hatched in the temperature range 10.0–14.2°C but the percentage decreased markedly to 39% at 5.9°C and 42% at 19.8°C. Hatching time (days after oviposition) decreased with increasing water temperature over the range 5.9–14.2°C and the relationship between the two variables was well described by a hyperbola. Therefore, the time taken for development was expressed in units of degree-days above a threshold temperature. Mean values (with 95%CL) were 552 (534–573) degree-days above 4.25°C for 10% of the eggs hatched, 862 (725–1064) degree-days above 3.57°C for 50% hatched and 1383 (1294–1486) degree-days above 3.14°C for 90% hatched. These values can be used to predict hatching times at temperatures below 14.68°C for 10% hatched, 14.54°C for 50% hatched and 14.45°C for 90% hatched. At higher temperatures, the hatching time and the number of degree-days required for development both increased with increasing temperature. Equations were developed to estimate the number of degree-days required for development at these higher temperatures.
Eggs were also placed in the Wilfin Beck, a small stony stream in the English Lake District. Maximum and minimum water temperatures were recorded in each week and the summation of degree-days was used to predict the dates on which 10%, 50% and 90% of the eggs should have hatched. There was good agreement between these estimates and the actual hatching times. Only 10–15% of the eggs hatched between October and late February with most of the eggs hatching in March, April and May. Nymphs hatching in October and November probably did not survive the winter.     

Bemerkungen zur Biologie sowie Haltung und Vermehrung des Sokotra-Riesengeckos, Haemodracon riebeckii (Peters, 1882)

The Socotra Giant Gecko, Haemodracon riebeckii, is the largest species of lizard on Socotra Island. The nocturnal, arboreal and rupiculous living geckos are omnivorous. Two pairs were kept in terrariums and were fed with various insects (crickets, locusts, cockroaches), sweet fruits and other feeding stuff (such as meat, fish). Temporarily H. riebeckii was kept together with other lizards (Eublepharis macularius, Trachylepis socotrana), without any signs of aggressive behaviour. Juveniles and adults of both sexes are able to produce a sound. These acoustic signals seem to be related to predators, because never any intraspecific function could be observed. Within seven years of captive breeding two females produced 253 eggs. Usually two white and sticky soft-shelled eggs were laid within one clutch, more rarely a single egg was laid. The two eggs of a clutch were always laid on the same day. H. riebeckii belongs to the geckos that bury their eggs and practice some brood care, but no special parental care. The female is able to proof with her hind legs the deep and shape of a hollow in the substrate to bury the eggs, which were buried in a sticky and soft-shelled condition. They are oval in shape (egg length 16.4-19.8 mm, egg width 12.4-17.8 mm, quotient EL:EW 1.22±0.05) and have in the beginning a weight ranging from 1.7100 to 2.5201 g. As typical for geckos with hard-shelled eggs the egg weight decreases during the incubation period. The loss can be between 5.59 to 30.29%. The development of eggs up to hatching of young depends upon temperature and the germinal stage in the laid egg. The time difference between the hatching of the young within one clutch of two eggs was usually 1 to 5 days. In some cases there were, however, longer differences (up to 61 days), which are probably caused by different developmental stages of the embryos during the time of egg laying. The shortest incubation period recorded during our investigations was 83 days for eggs incubated at constant temperature of 28 to 29.5 °C and the longest 359 days at 26 to 26.5 °C. Constant high incubation temperatures caused a premature hatching of young. In normal hatched young were the yolk sac retracted and the navel closed. In premature hatched young were the yolk not resorbed and the mortality within the first three month comparatively high. The snout-vent length (SVL) of newly hatched young is from 27 to 39 mm and the tail length (TL) from 25 to 38 mm (SVL:TL index 0.90-1.27), the weight is from 0.7688 to 1.5366 g. Young specimens are distinguished from adults by the brown/white striped lower jaw and the white-banded tail. Young which hatched in the terrarium were eaten by the adults. A loss of young can be avoided if they are raised individually.     

Synchrony in the hatching of eggs in the desert locust <Emphasis Type="Italic">Schistocerca gregaria</Emphasis> (Orthoptera: Acrididae): egg condition influences hatching time in the laboratory and under simulated field temperatures

This study examined the time of hatching of the desert locust Schistocerca gregaria Forskål (Orthoptera: Acrididae) in the laboratory to test the effect of eggs within a pod versus individualized eggs. The pod organization of eggs is thought to play a role in controlling hatching time and to facilitate synchronous hatching at constant temperatures. In the present study, we examined the hatching times of eggs in a pod and individualized eggs under 24-h thermocycles and simulated field temperatures. We tested two patterns of thermocycles consisting of a 12-h thermoperiod (35 or 30 °C) and 12-h cryoperiod (low temperature period; 30 or 25 °C), and two patterns of field temperatures observed in a natural habitat, Mauritania, in May and September. The majority of eggs hatched during low temperature periods in all patterns tested. In addition, the variances of hatching times for individualized eggs were significantly greater than for egg pods in which a clear peak of time of hatching was observed. We show that egg condition influences hatching time under thermocycles of constant and fluctuating temperatures in the laboratory, and may play a role in the adaptive time of hatching.     

Reproduction, growth and circadian activity of the snail Bradybaena fruticum (O. F. Müller, 1774) (Gastropoda: Pulmonata: Bradybaenidae) in the laboratory

Selected life cycle parameters of the snail Bradybaena fruticum were studied in the laboratory. The initial material for the laboratory culture was taken from a population in South Western Poland; the snails were kept in Petri dishes and plastic containers. The temperature, humidity and lighting conditions were maintained at a constant level (day 18°C, night 12°C, rh 80%, light:dark 12:12). Circadian activity observations were conducted outside the climatic chamber. Eggs — calcified, slightly oval, of mean dimensions 2.67x2.56 mm — were laid singly or in batches of 6–62, as a result of both biparental and uniparental reproduction. Incubation took 27–76 days and hatching was asynchronous. Hatching success was lower among eggs produced by single parents compared to eggs produced by two parents (c.a. 56 and c.a. 88%, respectively). Growth included fast (2.25 to 5 whorls) and slow (1.9–2.25 and >5 whorls) phases as well as lip formation, and took 261 to 420 days. The first eggs/batches were laid c.a. one year later, and for uniparentally reproducing snails the period was even longer. The growth of snails kept singly was faster than in those kept in groups. Juvenile snails were much more active than adults in the spring, summer and autumn but the adults were more mobile in the winter. In all seasons, juveniles were more active at night than adults.     

Temperature-controlled under-water egg dormancy and postflood hatching in Isotoma viridis (Collembola) as forms of adaptation to annual long-term flooding

Summary Incubation experiments with eggs of a population of Isotoma viridis, which is exposed to annual long-term flooding from about April to July, as well as field observations show that temperature controls both, underwater egg dormancy and immediate postflood hatching. The population is located at the Eder Freshwater Reservoir in Germany.If constant experimental temperatures are above 14°C, almost all eggs are nondormant. Dormancy is established at temperatures below 15°C, but embryonic development is completed. Experiments indicate that of the environmental factors that change drastically at the end of submergence (light, turgor pressure, oxygen, a.o.), only temperature acts as a hatching trigger. Hatching of the previously dormant eggs occurs at a constant threshold temperature of 16°C, mainly within 2 to 20 days after temperature elevation, but most of these eggs need even higher temperatures to hatch. Remaining eggs were partly stimulated to hatch by recooling them at 7°C for some days and then rewarming them again.The threshold temperatures observed are unusually high for Collembola and seem to be the result of selection by the special floodplain conditions. During normal years, the surface temperatures of submerged soil usually do not exceed threshold limits before summer drainage. This allows both, protection from under-water hatching and an optimal timing of hatching at the very beginning of the main terrestrial period. The experiments show that above the threshold temperature (in warm summers), individuals can hatch under water and survive submerged for 10–15 days. They can survive even longer in the water habitat, if emergent structures enable them to climb onto the water surface. Furthermore, a considerable polymorphism observed in some hatching properties improves the chance to survive under the unpredictable floodplain conditions.     

The production of subitaneous and diapause eggs: a reproductive strategy for Acartia bifilosa (Copepods: Calanoida) in Southampton Water, UK

Acartia bifilosa from Southampton Water lays two morphologically distinct types of egg which are described for the first time. Eggs with a smooth surface are considered subitaneous, while eggs covered with thick 'spines' are diapause. During the seasonal occurrence of A.bifilosa in Southampton Water, from November/December to June, subitaneous eggs are laid during the first months of this period. The production of diapause eggs is restricted to a 2 month period before A.bifilosa disappears from the water column. There are significant differences between the response of the eggs produced at seasonal field temperatures (5-12C) and those reported for other Acartia species. In particular, the numbers of eggs female^-1 day^-1, both subitaneous and diapause, are lower and typically <4; and the hatching time of subitaneous eggs is longer, at up to 10 days, at optimum temperatures between 15 and 20°C and optimum salinity >20 PSU. Females acclimated to higher laboratory temperature regimes show higher egg production rates at field salinity. A delayed-hatch subitaneous egg is also reported. Results suggest that fecundity in A.bifilosa from Southampton Water might be limited to some degree by temperature and the responses of the eggs produced appear to offer A.bifilosa a reproductive repertoire to ensure its sustained presence in this seasonally influenced environment.      

Sexual reproduction and diapause of Hexarthra sp. (Rotifera) in short-lived ponds in the Chihuahuan Desert

1. In the life cycle of monogonont rotifers it is generally assumed that diapausing eggs invariably hatch into amictic stem females which produce female offspring parthenogenetically. Diapausing eggs are only produced by later generations after sexual reproduction has been induced by environmental cues. 2. We show that populations of an undescribed Hexarthra species inhabiting small temporary ponds in the Chihuahuan Desert deviate from this life cycle pattern. These ponds may dry within days and up to 85% of females were mictic. Females producing male offspring and diapausing eggs were observed 1 or 2 days, respectively, after ponds had filled with water. 3. Under laboratory conditions, 7–46% of females hatching from re‐hydrated sediments were sexual. Male offspring of these females can fertilise other mictic stem females leading to diapausing egg formation. In laboratory experiments, females produced fully developed diapausing eggs within 1.9 days at 20 °C and 1.2 days at 30 °C. 4. In addition, embryonic development time (1.1–0.3 days at temperatures between 12 and 30 °C) and juvenile period (2.1–0.5 days for the same temperature range) are shorter than those of other rotifer species. In short‐lived habitats, the potential for rapid population development and production of new diapausing eggs may be crucial in the long‐term survival of populations.     

Phytophthora cryptogea root rot of tomato in rockwool nutrient culture:

The effect of root temperature on growth and yield of rockwool-grown tomato plants infected with Phytophthora cryptogea was investigated. Measurements of shoot and root growth were taken at high (25^oC) and low (15^oC) root temperatures during the generative phase of growth. The growth of roots of healthy and P. cryptogea-infected tomato plants in rockwool blocks was higher in plants grown with roots at 25^oC than at 15^oC after 60 days and a similar effect was found in slabs after 98 days. Under sub-optimal conditions for growth the disease became severe when root temperatures were low. Growth of roots was greatest when roots were maintained at a high temperature in combination with an ambient air temperature of c. 15^oC and the response was greater in cv. Counter than cvs Calypso and Marathon. Water-soluble carbohydrates of roots were higher in those produced in blocks than slabs and were reduced by infection compared to healthy plants with roots at 15^oC and 25^oC. Reduced transpiration rates were found 17 days after inoculation in symptomless plants grown at a root temperature of 25^oC. Infection, regardless of the temperature of the roots or cultivar, led to reduced stem growth. The plants grown at 25^oC were taller than those with a root temperature of 15^oC. After 9 wk of harvest, the cumulative fruit yields in infected cvs Counter and Calypso grown at 25^oC were comparable to that in healthy plants grown at either temperature and cumulative fruit numbers followed a similar pattern. High root temperatures led to delayed fruit ripening between weeks 3–10 and a larger number of unripe fruit. The weight of unripe fruit from infected plants grown at 25^oC at the terminal harvest was higher than from healthy plants with roots maintained at 15^oC.     

The effects of temperature on development of the large narcissus fly (Merodon equestris)

Eggs, larvae, pupae and adults of the large narcissus fly (Merodon equestris) were reared at a series of constant temperatures between 9–24°C. Egg development required from 37 days at 9°C to 7 days at 21.5°C. The low-temperature threshold for development was 6.7°C. Larvae reared at 1424°C were fully-grown after 18 weeks, but it took much longer for such insects to pupate, and adult flies emerged only after about 45 weeks of development. Large narcissus flies enter diapause during the larval stage and overwinter as fully-fed larvae, forming pupae in the following spring. Post-winter pupation and pupal development took from 169 days at 10°C to 36 days at 21.5°C. Of this, pupal development required from 91 days at 10°C to 19 days at 21.5°C. The low-temperature threshold for post-winter pupation and pupal development was 7.1°C, and for pupal development alone, 7.2°C. Females maintained at or below 19°C laid few eggs, whereas some females kept at or above 21.5°C laid more than 100 eggs (mean 69 ± 36). Approximately 50% of females maintained at or above 21.5°C laid less than 10 eggs during their lifetime. The mean egg-laying time was 6 to 9 days. Although temperatures at or below 19°C inhibited mating, once a female had mated, such temperatures did not prevent oviposition.     

Variation in the intensity of diapause in winter eggs of fruit tree red spider mite, Panonychus ultni

Winter eggs of Panonychus ulmi from six orchards in Kent showed a range of 3 weeks in the dates of 50 % hatch at field temperatures. From the effects of the duration and temperature of chilling, and the temperature of incubation, it was concluded that samples varied in their chilling requirement, and not in threshold temperatures for development. Diapause was terminated most effectively by chilling initially at o ^oC (for late-hatching strains) or 5 followed by 9 for the last month or two. Heritable variation in diapause intensity is discussed in relation to heat sums and the forecasting of hatch, and to phenology.     

Inactivation of cucumber mosaic virus in cultured tissues of Nicotiana rustica by diurnal alternating periods of high and low temperature

Cucumber mosaic virus (CMV) was inactivated in infected tissue cultures of Nicotiana rustica after periods of alternating high (32–40 ^oC) and low (22 ^CC) temperature. An increase in the incubation period at high temperatures resulted in greater virus inactivation but more rapid deterioration of the tissue cultures. Optimal programmes for virus inactivation and culture survival were 40 ^oC (8 h) +22 ^oC (16 h) per day for 12 or 18 days, 40 ^oC (16 h) + 22 ^oC (8 h) per day for 12 days or 36 ^oC (20 h) + 22 ^oC (4 h) per day for 12 days. Diurnal treatment periods of variable length and different high temperatures were related by using a concept of hour-degrees above a base temperature. Taking this base temperature as 25 ^oC a linear relation was found between the logarithm of virus infectivity and the number of hour degrees.     

Effects of temperature during chilling and pre-chilling periods on diapause and post-diapause development in a katydid, Eobiana engelhardti subtropica

In Eobiana engelhardti subtropica, early laid eggs reach the diapause stage in early autumn. For long periods before winter, the eggs are exposed to temperatures higher than their theoretical lower threshold for development. In contrast, late-laid eggs cannot reach their diapause stage before winter. Our study showed that E. e. subtropica copes with these difficulties via the thermal response involving embryonic diapause. In this katydid, the almost fully developed embryo undergoes an obligatory diapause. When diapause eggs were maintained at a temperature of 20 degrees C or higher, diapause persisted for a long time. Diapause was effectively terminated by temperatures ranging from 1 to 11 degrees C, and hatching occurred successfully at temperatures from 11 to 15 degrees C. In addition to the chilling temperature, pre-chilling temperature modified diapause intensity and hatching time. Diapause eggs hatched earlier after chilling when the pre-chilling temperature was lower, within a range of 14.5-25 degrees C. Thus, the low-temperature requirement for diapause termination prevents early laid eggs from untimely hatching in autumn, and low temperatures before and during winter decrease diapause intensity and shorten the hatching time in the following spring. When eggs were chilled before diapause, they tolerated chilling and averted diapause. Thus, even if eggs encounter low temperatures before diapause, they can hatch in the following spring.