THE EFFECTS OF TEMPERATURE ON THE DEVELOPMENT OF THE FREE-LIVING STAGES OF DOCHMOIDES STENOCEPHALA (RAILLIET, 1884) (ANCYLOSTOMIDAE: NEMATODA)

1959 ◽  
Vol 37 (3) ◽  
pp. 247-257 ◽  
Author(s):  
H. C. Gibbs ◽  
K. E. Gibbs

The effects of temperature on the development of the free-living stages of Dochmoides stenocephala (Railliet, 1884) have been studied using agar cultures. Development was obtained at as low a temperature as 7.5 °C. The optimum temperature for the free-living stages was considered to be 20 °C. The time of development of the larvae to the infective stage was inversely proportional to the ambient temperature between the limits of 7.5 °C and 27 °C.

1959 ◽  
Vol 37 (3) ◽  
pp. 305-316 ◽  
Author(s):  
Devandra Prasad

The optimum temperature for development of Trichostrongylus retortaeformis is about 25 °C in a wet faecal culture, when the infective stage is reached in from 3 to 5 days, but at 3 to 5 °C a few larvae can develop in 8 to 10 weeks, and infective larvae can survive for 13 weeks. Both eggs and larvae can survive desiccation for considerable periods.


1961 ◽  
Vol 39 (1) ◽  
pp. 47-53 ◽  
Author(s):  
S. P. Gupta

The effects of temperature on the survival and development of the free-living stages of Trichostrongylus retortaeformis have been studied using agar cultures inoculated with pure cultures of Escherichia coli. The ova hatched and infective larvae developed at temperatures ranging from 5 °C to 30 °C, but 35 °C was lethal in 24 hours. The time of development of the larvae to the infective stage was inversely proportional to the ambient temperature between the limits of 10 °C and 30 °C. The longevity in water of third-stage larvae previously cultured at 20 °C, 25 °C, and 30 °C was studied at temperatures ranging from 5 °C to 40 °C.


1990 ◽  
Vol 259 (2) ◽  
pp. R204-R209 ◽  
Author(s):  
E. D. Stevens ◽  
R. E. Godt

Contractile performance decreases with a decrease in temperature and increases with an increase in pH. In general, a decrease in ambient temperature is associated with an increase of the pH of the intracellular and extracellular fluids of ectotherms. Thus the concomitant increase in pH will to some extent counteract the effect of the decrease in temperature. We review the magnitude of this effect and show that it is modest for force (24%) but is small or negligible for speed or for variables involving time. Experiments with skinned fibers yield similar results to those with intact fibers. We argue that one important effect of the concomitant increase in pH is that it causes an increase in calcium sensitivity and that there may be a considerable metabolic saving associated with releasing less calcium at lower temperatures.


Forests ◽  
2021 ◽  
Vol 12 (4) ◽  
pp. 432 ◽  
Author(s):  
Melody A. Keena ◽  
Paul M. Moore ◽  
Gregg Bradford

Anoplophora chinensis (Forster) is an invasive species that can damage many tree species in orchard, urban, and forested habitats. Adult survival, reproduction, and egg hatch of A. chinensis from Italy and China are evaluated at eight constant temperatures (5, 10, 15, 20, 25, 30, 35, and 40 °C) under laboratory conditions. The estimated Tmax for longevity was 42 and 33 °C for females and 42 and 39 °C for males from China and Italy, respectively. The estimated Tmax, Tmin, and optimum temperature for fecundity were 35, 9, and 29 °C, respectively. Females laid eggs at 15–30 °C and eggs hatched at 15–35 °C. Days to first oviposition increased exponentially from 13 days at 30 °C to >300 days near 10 °C. The estimated Tmin for egg hatch was 13 °C, the Tmax at 38 °C, and the optimum 29 °C. Percentage hatch was estimated to be highest at 26 °C and have a Tmax of 31 °C and Tmin of 10 °C. These results indicate that summer temperatures over a wide range of latitudes should support beetle survival and reproduction, but at temperatures ≥35 °C, oviposition ceases, and adult survivorship declines. In addition, females may survive into the fall, but lay fewer eggs that may not hatch. These responses of A. chinensis to temperature can be used for developing phenological models to predict the timing of stages for management or eradication efforts.


1958 ◽  
Vol 36 (4) ◽  
pp. 623-628 ◽  
Author(s):  
Premvati

The optimum temperature for the complete development of the free-living and the infective larvae of Strongyloides fülleborni is 25 °C. Morphological changes are seen at higher or lower temperatures.


Parasitology ◽  
1963 ◽  
Vol 53 (3-4) ◽  
pp. 469-481 ◽  
Author(s):  
J. H. Rose

Outdoor observations were made on the rate of development of the free-living stages of H. contortus at different times of the year, and on the migratory activities and longevity of the larvae in faeces, on herbage and in soil.The effects of temperature and humidity on the survival and development of eggs and larvae, both in faeces and when separated from the faeces, were studied in the laboratory.The results of these observations are discussed in relation to the heavy mortality of the free-living stages of H. contortus and to the transmission of infection in the field.


2001 ◽  
Vol 31 (5) ◽  
pp. 839-842 ◽  
Author(s):  
Clóvis de Paula Santos ◽  
Terezinha Padilha ◽  
Maria de Lurdes de Azevedo Rodrigues

The effect of different temperatures on the predatory activity of Arthrobotrys oligospora and Duddingtonia flagrans on the free-living larval stages of cyathostomes were evaluated in an experiment where feces of horses containing the parasites’ eggs were treated with these fungi and incubated under different constant temperatures (10°C, 15°C, 20°C, 25°C and 30°C ). The results indicated that the optimum temperature for egg development was 25°C. At 10°C the number of L3 recovered was practically zero, and at 15°C and 20°C, the percentage of larvae recovered was less than 3% of the total number of eggs per gram of feces. When these cultures subsequently were incubated for an additional period of 14 days at 27°C, they allowed the development of L3. In all the cultures inoculated with fungi a significant reduction in the number of larvae was observed. When incubated at 25°C or 30°C, the fungi caused reductions above 90%, in the number of L3. The samples cultivated at 10°C, 15°C, 20°C, 25°C and 30°C, when incubated for an additional period of 14 days at 27°C the reduction percentage of larvae was above 90% for A. oligospora. However, the same did not occur for D. flagrans. Here a reduction percentage between 47.5% and 41.8% was recorded when the cultures were incubated at 10°C and 20°C, respectively. The two species of fungi tested showed to be efficient in reducing the number of L3 when mixed with equine feces and maintained at the same temperature for the development of larval pre-parasitic stages of cyathostomes.


2008 ◽  
Vol 422 (1) ◽  
pp. 321-323
Author(s):  
T. B. Kalinnikova ◽  
A. Kh. Timoshenko ◽  
D. Yu. Galaktionova ◽  
T. M. Gainutdinov ◽  
M. Kh. Gainutdinov

2009 ◽  
Vol 99 (9) ◽  
pp. 1045-1052 ◽  
Author(s):  
Paul W. Tooley ◽  
Marsha Browning ◽  
Kerrie L. Kyde ◽  
Dana Berner

We investigated the temperature and moisture conditions that allow Phytophthora ramorum to infect Rhododendron ‘Cunningham's White’. Most experiments were performed with a single P. ramorum isolate from the NA1 clonal lineage. For whole plants incubated in dew chambers at 10 to 31°C, the greatest proportion of diseased leaves, 77.5%, occurred at the optimum temperature of 20.5°C. Disease occurred over the entire range of temperatures tested, although amounts of disease were minor at the temperature extremes. For whole plants exposed to varying dew periods at 20°C and then incubated at 20°C for 7 days, a dew period as short as 1 h resulted in a small amount of disease; however, at least 4 h of dew were required for >10% of the leaves to become diseased. Moisture periods of 24 and 48 h resulted in the greatest number of diseased leaves. In detached-leaf, temperature-gradient-plate experiments, incubation at 22°C resulted in the greatest disease severity, followed by 18°C and then 14°C. In detached-leaf, moisture-tent experiments, a 1-h moisture period was sufficient to cause disease on 67 to 73% of leaves incubated for 7 days at 20°C. A statistical model for disease development that combined the effects of temperature and moisture period was generated using nonlinear regression. Our results define temperature and moisture conditions which allow infection by P. ramorum on Cunningham's White rhododendron, and show that P. ramorum is able to infect this host over a wide range of temperatures and moisture levels. The results indicate that P. ramorum has the potential to become established in parts of the United States that are outside its current range.


1947 ◽  
Vol 24 (1-2) ◽  
pp. 79-94
Author(s):  
L. E. S. EASTHAM ◽  
F. SEGROVE

1. The effects of temperature and humidity on the duration of each instar of the life cycle of Calandra granaria Linn. have been examined. The insects were reared at temperatures ranging from 15 to 30° C. and at atmospheric humidities ranging from 40 to 80% R.H. 2. A method is described for assessing the effect of temperature as an independent factor. 3. The temperatures employed fall within the ‘vital zone’. Extrapolation indicates the threshold temperature to be approximately 11° C. for the egg and larval instars though somewhat lower for the pupa. 30° C. is below the optimum temperature. 4. The durations of the egg and pupal stages are not affected by atmospheric humidity. 5. The duration of all larval instars is affected by moisture. It is suggested that this is largely due to atmospheric humidity and that food water is of little significance. 6. Shortage of moisture acts as an obstacle to development. Evidence is presented which indicates that drier atmospheres tend to desiccate the insect and that desiccation is responsible for retarded growth and development. 7. Since much earlier work on temperature and moisture has been done on fasting insects and, therefore, on insects deficient in one of the most important environmental factors, we suggest that our results, incomplete as they are, indicate the need for new approaches to be made. More complete data on feeding insects under controlled conditions of food, temperature and moisture are required, from which can be drawn up more complete balance sheets of development involving measurements of food utilization and respiratory rates.


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