Thermal inactivation of cherry leaf roll virus in tissue cultures of Nicotiana rustica raised from seeds and meristem-tips

Nicotiana rustica tissue cultures derived from seeds or embryos infected with cherry leaf roll virus (CLRV), remained infected after culture at 22 ^oC. No infectivity was found in cultures held at 32 ^oC for 5 days but it was readily detected after such cultures were transferred to 25 ^oC for 8 days. Virus was permanently eradicated from most plants after 20 days incubation at 32 ^oC and from all plants after 7 days incubation at 40 ^oC. Partially purified preparations of CLRV lost infectivity after 9–12 days at 22^oC, 5 days at 32^oC and 3 days at 40^oC.     

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.     

Effect of high soil temperatures on nodulation of cowpea, Vigna unguiculata

Cowpeas, inoculated with one of five effective strains of Rhizobium isolated from African soils, were grown at root temperatures of 30 ^oC continuously or at 36, 38, 40, 42 and 44 ^oC for 5 h/day and returned to glasshouse ambient for the intermediate period. Growth was best at 30 and 36 ^oC; above 40 ^oC growth was poor and no nodules formed. At 40 ^oC two strains failed to nodulate. Symbiotic performance was not dependent only on nodule production as nodule efficiency varied inversely with temperature. The number of nodules formed by strain R5000 after exposure of inoculated seed or seedlings to 40,42 or 44 ^oC for 5 h/day on each of 3 or 6 days depended on the age of plant and the duration of exposure to stress. When exposed to 42 or 44 ^oC during the first 3 days after sowing nodulation was reduced from 18 to 1–3 nodules/plant even after a further 40 days growth at ambient (30 day, 20 ^oC night). Nodulation was unaffected when 10–15-day-old seedlings were exposed to the same conditions. Numbers of strain R5000 on seed declined rapidly following three daily exposures of 5 h at 39 and 42 ^oC; at 45 ^oC less than three bacteria survived on each seed. Other rhizobia of the cowpea group varied greatly in their toleration of high temperatures, some survived well at 45 ^oC whereas others behaved like R5000.     

High temperature inactivation of cucumber and alfalfa mosaic viruses in Nicotiana rustica cultures

Cucumber mosaic (CMV) and alfalfa mosaic (AlfMV) viruses could not be detected in Nicotiana rustica tissues cultured at 32 °C for 16–18 days or at 40 °C for 5 days, but infectivity remained high in comparable tissue cultured at 22 °C. Incubation of infected cultures at 28–30 °C resulted in an initial reduction followed by a partial recovery in the infectivity of both viruses. The infectivity of CMV in tissues grown between 12 and 32 °C was highest in cultures grown at 12 °C. Although CMV infectivity was not detected in cultures after 16–18 days at 32 °C, virus was eliminated only after a further 30 days at 32 °C. When cultures were transferred from 32 to 22 °C after shorter treatment periods, infectivity rapidly increased to levels higher than those of infected tissues grown continuously at 22 °C. At 40 °C, CMV was eliminated from infected tissues after 9 days and AlfMV after 7 days. Cultures grown continuously at 40 °C deteriorated rapidly but, when grown under diurnal alternating periods of 8 h at 40 °C and 16 h at 22 °C, they remained viable and CMV was also inactivated.     

Elimination in vitro of two Grapevine Nepoviruses by an Alternating Temperature Regime*

A 40 day in vitro treatment with 6 h at 39°C followed by 18 h at 22°C was effective in eliminating both grapevine fanleaf virus (GFLV) and arabis mosaic virus (AMV) from the developing shoot tips (2 mm) of grapevine shoot tip cultures. Longer treatment durations with consecutive 12 h periods at 35°C and 22°C eliminated GFLV in some cases, but did not eliminate AMV.     

Persistence of Viruses in Desert Soils Amended with Anaerobically Digested Sewage Sludge

Pima County, Ariz., is currently investigating the potential benefits of land application of sewage sludge. To assess risks associated with the presence of pathogenic enteric viruses present in the sludge, laboratory studies were conducted to measure the inactivation rate (k = log₁₀ reduction per day) of poliovirus type 1 and bacteriophages MS2 and PRD-1 in two sludge-amended desert agricultural soils (Brazito Sandy Loam and Pima Clay Loam). Under constant moisture (approximately -0.05 × 10⁵ Pa for both soils) and temperatures of 15, 27, and 40°C, the main factors controlling the inactivation of these viruses were soil temperature and texture. As the temperature increased from 15 to 40°C, the inactivation rate increased significantly for poliovirus and MS2, whereas, for PRD-1, a significant increase in the inactivation rate was observed only at 40°C. Clay loam soils afforded more protection to all three viruses than sandy soils. At 15°C, the inactivation rate for MS2 ranged from 0.366 to 0.394 log₁₀ reduction per day in clay loam and sandy loam soils, respectively. At 27°C, this rate increased to 0.629 log₁₀ reduction per day in clay loam soil and to 0.652 in sandy loam soil. A similar trend was observed for poliovirus at 15°C (k = 0.064 log₁₀ reduction per day, clay loam; k = 0.095 log₁₀ reduction per day, sandy loam) and 27°C (k = 0.133 log₁₀ reduction per day, clay loam; k = 0.154 log₁₀ reduction per day, sandy loam). Neither MS2 nor poliovirus was recovered after 24 h at 40°C. No reduction of PRD-1 was observed after 28 days at 15°C and after 16 days at 27°C. At 40°C, the inactivation rates were 0.208 log₁₀ reduction per day in amended clay loam soil and 0.282 log₁₀ reduction per day in sandy loam soil. Evaporation to less than 5% soil moisture completely inactivated all three viruses within 7 days at 15°C, within 3 days at 27°C, and within 2 days at 40°C regardless of soil type. This suggests that a combination of high soil temperature and rapid loss of soil moisture will significantly reduce risks caused by viruses in sludge.     

Effects of Indoleamines and Short Photoperiods on the Encystment of Gonyaulax polyedra

At a temperature of 15^oC, Gonyaulax polyedra responds to short days (light ≤ 10 h) by transition to the stage of a resting cyst. At 20^oC, even an lightdark (LD) cycle of 6:18 is incapable of inducing this process. In otherwise cyst-inducing conditions (15^oC; 10 h of light per day), an interruption of the scotophase by 2 h of light (LDLD 8:2:2:12 or 2:2:8:12) prevented encystment. Cyst induction is, therefore, initiated by a photoperiodic mechanism rather than by light deficiency. In Gonyaulax, photoperiodism may be mediated by the action of indoleamines. Melatonin, which exhibits a circadian rhythmicity in this organism, leads to encystment when given 1 h before lights-off in LD 11:13 at 15^oC, i.e., under otherwise noninducing conditions. Again, at 20^oC, melatonin is inefficient. Some analogues of melatonin, in particular, 5-methoxytryptamine and N,N-dimethyl-5-methoxytryptamine, and, at high concentrations, their respective precursors, serotonin and bufotenin, are capable of inducing cyst formation at 20^oC and in LD 12:12, whereas A'-acetyl-serotonin does not show this effect.     

Effects of virus genotype and temperature on seed transmission of nepoviruses

Transmission of different nepoviruses through chickweed (Stellaria media) seed was differently affected by ambient temperature during seed production. Raspberry ringspot and tomato black ring (Scottish isolate) viruses were similarly and frequently transmitted at 14 , 18 and 22 ^oC, whereas arabis mosaic virus was transmitted most frequently at 14 ^oC, and strawberry latent ringspot and tomato black ring (German isolate) viruses at 22 ^oC. When infected by seed-borne nepoviruses, seedlings of S. media and other species were symptomless at 15–25 ^oC, and the viruses were therefore detected by inoculating sap to Chenopodium quinoa indicator plants. However, typical symptoms of arabis mosaic and tomato black ring viruses were induced by growing Nicotiana tabacum, N. clevelandii and C. quinoa seedlings infected with seed-borne virus at 33–37 ^oC during the third and fourth weeks after sowing, preceded and followed by periods at 15–25 ^oC. The proportion of N. tabacum seedlings developing symptoms was the same as that of untreated seedlings yielding sap-transmissible virus. Seed transmissibility of pseudo-recombinant isolates of raspberry ringspot and tomato black ring viruses, containing RNA-i from one virus strain and RNA-2 from another strain, depended greatly on the transmissibility of the strain contributing RNA-i. The source of RNA-2 had an additional but smaller influence. The satellite RNA (RNA-3) of tomato black ring virus was seed-transmitted in S. media and its occurrence in cultures did not affect the frequency of transmission of the virus. Results of testing the infectivity of extracts of seed from infected mother plants suggested that failure of seed transmission reflected failure to become established in the seed, not subsequent inactivation. Whereas seed transmissibility of raspberry ringspot virus is primarily dependent on information carried in RNA-i, transmissibility by nematode vectors, another property of major ecological importance, is determined by RNA-2. In the field, selection pressures presumably can act independently on the two parts of the genome but evidence was also obtained of selection for mutual compatibility of RNA-i and RNA-2.     

The effect of temperature on viability of imbibed weed seeds

Imbibed seed of 10 common arable weeds were placed in trays in initially moist soil and, after imbibing for 2h, heated in ovens/incubators set to 31^oC, 42^oC, 56^oC, 75^oC or 100^oC for 0.5, 1, 2, 4, 8 or 16 days or at 102^oC, 155^oC, 204^oC or 262^oC for 0.5, 1, 2, 5, 7.5 or 10 min. After heating, seeds were incubated for 28 days at 10/20^oC or 20/30^oC on a 12 h dark/light regime, depending on species, and germination recorded. At the lower temperatures, germination of all species was prevented by temperatures of 75^oC or higher for periods of 0.5 days or more. Germination was lower after treatment at 56^oC than at 31^oC or 42^oC for all species except Rumex obtusifolius. The maximum temperature required to prevent germination varied among species and was of greater importance than the duration of heating. Germination was variable with duration of heating. At the higher temperatures, there was very little germination of any species after heating at 204^oC for 7.5 min or 262^oC for 5 min or more. Seeds were greatly buffered from the air temperature by 3 mm of soil, throughout the shorter duration of heating. The average temperature of the soil, over the 10 min heating required to prevent over 90% germination, varied among species and ranged from 48^oC for Avena fatua to 65^oC for R. obtusifolius. This work implies that composting systems maintained at 65^oC are unlikely to provide an efficient method of weed control. Recommendations for improvement of the laboratory technique are suggested.     

Effect of temperature on virus eradication and growth of infected tissue cultures

Cucumber mosaic (CMV) and alfalfa mosaic (AlfMV) viruses were eradicated or their concentrations greatly diminished when infected meristem tips were grown in static or shake culture at 32 or 34 ^oC. Similar cultures grown at 22 ^oC remained infected. Tobacco mosaic virus (TMV) was not eradicated from shake cultures at 32 ^oC and the concentration of TMV in such cultures at 32 ^oC was sometimes higher than at 22 ^oC. The concentration of CMV and AlfMV was considerably less in cultured tissues than in infected leaf material, but that of TMV was similar. Cultures infected with CMV or TMV grew more slowly than healthy cultures. Growth of AlfMV infected and healthy cultures was similar.     

Effects of daylength and day/night temperatures on growth and seed yield of cowpea cv. K 2809 grown in controlled environments

The effects of climatic factors on the growth, reproductive development and seed yield of cowpea (cv. K 2809) were investigated in controlled environment cabinets. Plants were grown to maturity in eight environments comprising all combinations of two day lengths (11 h 40 min and 13 h 20 min), two day (27 and 33 ^oC) and two night (19 and 24 ^oC) temperatures. The plants were nodulated (Rhizobium strain CB 756) and received 197 ppm N throughout growth. Treatments changed the time to the appearance of first flowers by a maximum of 6 days but the later-flowering plants more than doubled their dry weight during this period, so that effects on plant form and, ultimately, seed production were considerable. Warm nights (24 ^oC) not only hastened the onset of flowering but also enhanced dry matter production during the pre-flowering period; they did not extend the total growing period. Warm days (33 ^oC) did not enhance dry matter production but shortened the duration of the growing period by an average of 21 days (20%). Variation in final seed yield was mainly due to differences in the number of pods borne on branches. Warm days markedly decreased the number of pods per plant (an overall average reduction of 49%) as did warm nights in conjunction with the long (13 h 20) daylength. The number of seeds per pod was effected only by daylength (8.3 and 7.6 seeds in the long and short daylengths, respectively). Mean seed weight was decreased by 19% in warm as compared to cool nights but was increased by 18% in warm as compared to cool days. These responses are compared with those obtained with soyabean cv. TK5 in a previous experiment and are shown, in general, to be similar.     

Effects of short episodes of heat stress on flower production and fruit-set of groundnut (Arachis hypogaea L.)

Groundnuts (Arachis hypogaea L.) are an important crop of the semi-arid tropics where they are often exposed to maximum temperatures of > 40 degrees C for short periods during the growing season. The objectives of this study were to determine: (i) the effects of short periods of exposure to high temperature on flower production (FN), the proportion of flowers forming fruits (fruit-set) and the number of pegs and pods per plant (RNt); (ii) whether fruit-set is affected by high temperature during different periods of daylight in each diurnal cycle; and (iii) whether responses to temperature were qualitative or quantitative. Plants of cv. ICGV 86015 were grown in controlled environments at a day/night temperature of 28/22 degrees C from sowing until 9 d after flowering (DAF). Then, cohorts of plants were: (a) exposed to day temperature of 28, 34, 42 or 48 degrees C for 2, 4 or 6 d; or were (b) exposed to 34, 42 or 48 degrees C for 6 d either throughout a 12 h day (08.00 to 20.00 h, WD), or only during the first 6 h (AM) or second 6 h (PM) of the day. Values of RNt were significantly reduced by high temperature, by duration of exposure, and by timing of exposure. Variation in FN was quantitatively related to floral bud temperatures during the day over the range 28-43 degrees C. In contrast, only floral bud temperatures > 36 degrees C during AM and WD significantly reduced fruit-set and hence RNt, whereas high PM temperature had no effect on fruit-set. These findings indicate that the response of RNt to day temperature is quantitative and can be modelled by combining the responses of FN and fruit-set to temperature.     

Photoperiodic induction of diapause in the spider mite Tetranychus urticae: qualitative or quantitative time measurement?

Abstract. Insects and mites may measure photoperiods eitfier by classifying them as long or short relative to a critical value (qualitative time measurement) or by using the absolute value (quantitative time measurement). The spider mite Tetranychus urticae is thought to use a qualitative mechanism of time measurement. In this paper we present the results of experiments with an inbred line of the spider mite (to keep genetic variation in photoperiodic responses small), to test whether quantitative aspects also play a role. Differences in diapause incidence in different long-night photoperiods at different temperatures may be an indication of quantitative responses to photoperiod. The effect of temperature on the photoperiodic response curve was studied at 16^oC, 19^oC and 22^oC. The response curves appeared to be similar at 16^oC and 19^oC, with a critical nightlength between 10 and 11 h. At 22^oC, diapause induction was less than 100% in all long-night regimens and die critical nightlength had shifted to 12 h. Maximum diapause induction (93%) occurred in a light-dark cycle with a 16 h dark phase (LD 8:16 h). Diapause induction was lowest in long-night photoperiods with dark phases of 20 h and longer. The number of light-dark cycles needed for 50% diapause induction at 19^oC varied. between 12.1 and 14.7 for LD 6:18 h, between 10.9 and 12.5 for LD 8:16 h, between 10.6 and 11.6 for LD 10:14 h, and between 10.1 and 10.7 for LD 12:12 h. Independent of die light-dark regimen, diapause induction took place in some individuals after receiving 8 cycles and virtually all individuals entered diapause after 16 cycles. No effect was found of the photoperiodic treatment during prediapause development (LD 6:18 h, LD 8:16 h, LD 10:14 h, LD 12:12 h) on diapause duration. The average diapause duration at LD 10:14 h and 19^oC was 61 days over all four treatments. We explained the results by hypothesising that nightlengths are assessed qualitatively and mat the photoperiodic clock operates more accurately near the critical nightlength.     

Temperature modulates the Ca current of HIT-T15 and mouse pancreatic β-cells

The effects of raising temperature on the Ca²⁺, currents of insulin-secreting HIT and mouse pancreatic β-cells were studied. Currents were measured in 3 mM Ca²⁺ containing solutions using standard whole-cell techniques. Increasing temperature from 22°C to 35°C increased peak Ca²⁺, current amplitude, percent (fast) inactivation and decreased the time-to-peak of the current. Ca²⁺ currents in HIT and mouse β-cells responded in the same manner to an imposed physiological burstwave with test-pulses: (i) application of the burstwave inactivated the test-pulse Ca²⁺ current at both high and low temperatures; (ii) Ca²⁺, current inactivation leveled off during the plateau phase at 20–22°C whereas there was an apparent continual decay at 33–35°C; and (iii) recovery from inactivation occurred during the interburst period at both temperatures. Application of a physiological burstwave without test-pulses to mouse β-cells before and after addition of 0.2 mM Cd²⁺ resulted in a Ca²⁺ difference current. This current activated during the hyperpolarized interburst phase, activated, inactivated and deactivated rapidly and continually during the plateau phase, and recovered from inactivation during the interburst. Although raising temperature strongly modified HIT and mouse β-cell Ca²⁺ current, our work suggests that other channels, in addition to Ca²⁺ channels, are likely to be involved in the control of islet bursts, particularly at different temperatures. In addition, the effect of temperature on islet cell Ca²⁺, current may be partly responsible for the well-known temperature dependence of glucose-dependent secretion.     

Growth and development of soyabean cv. TK5 as affected by tropical daylengths, day/night temperatures and nitrogen nutrition

Two experiments were done in Saxcil growth cabinets in order to investigate the effects of climatic factors and nitrogen nutrition on the growth, reproductive development and seed yield of soyabean cv. TK5. In the first, plants were grown to maturity in eight environments comprising all combinations of two short daylengths (11 h 40 min and 13 h 20 min), two day (27 and 33^oC) and two night (19 and 24^oC) temperatures. In the second, day temperature was kept at 33^oC but the night temperature was varied (19 and 24^oC) as was the mineral nitrogen supply (20 and 197 ppm N) to plants which were either inoculated or not with an effective single strain of Rhizobium. Taller, more branched, later flowering plants were produced in the longer daylength but seed yield was hardly affected because the components of yield did not all respond similarly. In the higher day temperature treatments seed yield per plant was reduced by half because all yield components were adversely affected - pods per plant by 34 %, mean seed dry weight by 24 % and seeds per pod just slightly. There was a marked effect of the higher night temperature which promoted early vegetative growth, induced early flowering and although the number of pods per plant was, overall, reduced by 48 %, seed yield per plant was little affected as mean seed dry weight was increased by 37 % and the number of seeds per pod was also increased slightly. Prior to flowering, nodulated plants obtained about two thirds of their total nitrogen requirement via direct uptake and one third through the symbiotic system. Vegetative dry weight and plant nitrogen content were increased by the higher mineral nitrogen level and, although height was slightly diminished, more branches were produced. Seed yield, however, was only slightly increased. These experiments have shown that night temperature is an environmental factor of major importance for the growth of this soyabean cultivar. They have provided, also, a more rational basis for interpreting seasonal variations in growth and seed yield of soyabean in the tropics where, clearly, day and night temperature effects can override those of daylength and nitrogen nutrition.     

Stemphylium botryosum f. lactucae- its developmentjn vifro and its pathogenicity to lettuce leaves

Stemphylium botryosum f. lactucae, incitant of a leaf-spot disease of stored lettuce, was found to be relatively restricted in its host range. Cross-inoculations with spore suspension of this fungus failed to induce symptoms in any of the host plants tested, except carrot. Among isolates of S. botryosum from various hosts, only the isolate from carrot induced slight symptoms on lettuce. While mycelial growth of the lettuce isolate was confined to the range 13–37 ^oC spores germinated at more extreme temperatures. The optimum temperature for germination and for radial growth on PDA was found to be between 25 and 30 ^oC. Wet spores were quickly inactivated at 50 ^oC, whereas more than 40 % of dry spores withstood a 24 h exposure to that temperature. Only the outer leaves of lettuce responded readily to inoculation with a spore suspension, the required incubation period being 3 days at 25 ^oC. Symptoms developed less readily on bruised leaves. Relative humidity approaching saturation was necessary for prompt and typical infection, notably during the 24 h following inoculation. Short dry periods (60 % r.h.) interposed at a later stage, while somewhat inhibitory, did not prevent infection.     

Stability of ectromelia virus strain NIH-79 under various laboratory conditions

Ectromelia virus strain NIH-79 was suspended in fetal bovine serum (FBS), minimum essential medium, Hanks' base plus 10% FBS (MEMH + FBS), phosphate-buffered saline (PBS) or PBS plus 50% glycerol (PBS + G). Suspensions were held as liquids or as dry spots at various temperatures. Virus was most stable in FBS and least stable in PBS + G at 4 degrees C, room temperature (23-25 degrees C) or 37 degrees C. Virus held at 4 degrees C was more stable than virus held at higher temperatures, irrespective of supporting medium. Dried spots of blood or serum from ectromelia virus-infected mice remained infectious at room temperature for 11 days and 4 days, respectively. Dried spots of FBS that contained virus were infectious for 5 days, whereas virus retained infectivity for 1 day after drying in other media. Virus was inactivated completely in 10% serum in PBS exposed to 60 degrees C for 30 minutes. Virus was inactivated completely in slices of infected liver and spleen immersed in 10% neutral buffered formalin for 20 hours. These results show that the stability of ectromelia virus strain NIH-79 is medium and temperature dependent and that rapid inactivation occurs after treatments routinely used in diagnostic and research procedures.     

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.     

Early warning of egg hatching in pea moth (Cydia nigricana)

Female pea moths (Cydia nigricana) kept at 23 ^oC began to lay eggs 2–3 days after emergence, lived for 16–21 days and laid on average 71 eggs. Individuals kept in field cages lived for slightly longer and laid on average 91 eggs. About 85% of eggs were laid during the first 11 days of the oviposition period, usually in the late afternoon and early evening. The relationship between the rate of egg development and temperature was defined. The estimated developmental zero was 9-4 ^oC at constant temperatures and 8-5 ^oC at fluctuating temperatures. Above 28 ^oC mortality increased and above 31 ^oC development was apparently retarded. Development at constant temperatures took 6–16% longer than at fluctuating temperatures with the same mean. Estimates of hatching dates in the field made from temperature data recorded at several sites in and near a pea crop, and 8 km distant, were usually within a day of the observed date. In warm weather, estimated and observed dates usually coincided; in cooler weather hatching was 2–3 days later than expected. Hatching dates predicted from temperature data after only 80% of development had occurred were correct on 28 out of 36 occasions. An example is given to show how the method could be used eventually with a sex attractant trapping system to provide early warning of first hatching and spraying dates.