首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 31 毫秒
1.
All life-stages ofSarcoptes scabiei var.canis survive in the hosts' environment for several days to several weeks depending on r.h. and temperature. Survival of larvae was comparable to males; survival of nymphs was comparable to females. Females and nymphs generally survived longer than larvae and males.Low temperature (10–15°) and high r.h. prolonged survival of all life stages. At 10–15°C, females and nymphs survived 1–3 weeks at 97% r.h., 1–2 weeks at 75% r.h. and 5–8 days at 45% r.h. At 20–25°C, survival was significantly reduced but all life-stages survived at least 2 days at 25% r.h. and 5–6 days at 75–100% r.h. Long survival off the host coupled with host-seeking behavior of these mites make it likely that environmental contamination is a source of scabies in domestic and wild mammals, and in humans.  相似文献   

2.
The effect of temperatureon conidial germination, mycelial growth, andsusceptibility of adults of three tephritidfruit flies, Ceratitis capitata(Wiedemann), C. fasciventris (Bezzi) andC. cosyra (Walker) to six isolatesof Metarhizium anisopliae were studied inthe laboratory. There were significantdifferences among the isolates in the effect oftemperature on both germination and growth.Over 80% of conidia germinated at 20, 25 and30°C, while between 26 and 67% conidiagerminated at 35°C and less than 10% at15°C within 24 hours. Radial growth was slowat 15°C and 35°C with all of theisolates. The optimum temperature forgermination and mycelial growth was 25°C. Mortality caused by the six fungal isolatesagainst the three fruit fly species varied withtemperature, isolate, and fruit fly species.Fungal isolates were more effective at 25, 30and 35°C than at 20°C. The LT90values decreased with increasing temperature upto the optimum temperature of 30°C. Therewere significant differences in susceptibilitybetween fly species to fungal infection at allthe temperatures tested.  相似文献   

3.
The ability of Rhizoctonia solani AG‐1 IA, the causal agent of rice sheath blight, to survive in diseased rice straw and as sclerotia and mycelia was investigated. After storage for 10 months at 4°C, 25°C and non‐air‐conditioned natural room temperature (NRT, temperature range from 6°C to 35°C), sclerotia placed inside a desiccator, soaked in sterile water or immersed in wet paddy soil were viable. In contrast, only 15% of sclerotia in dry paddy soil survived. Survival of mycelia was severely affected by temperature and humidity. After 10 months in a desiccator at 4°C, 55% of mycelia samples could survive, whereas at 25°C and NRT, mycelial samples survived for only 7 and 5 months, respectively. However, mycelia stored in sterile water at constant temperatures (4°C or 25°C) survived for 10 months. A certain amount of UV radiation had no obvious effect on the survival of sclerotia or mycelia. The survival rate of the fungus in diseased rice straw stored for 16 months could reach 100% at 4°C, 50% at 25°C and 35% at NRT. The survival rates of the pathogen in diseased rice straw buried in dry, wet and flooded paddy soils after 10‐month storage at NRT were 75, 100 and 100%, respectively, indicating that soil humidity is a crucial factor for the survival of this fungus.  相似文献   

4.
Ballal  Chandish R.  Singh  S. P.  Jalali  S. K.  Kumar  Pradyumn 《BioControl》1989,34(4):463-468
Cold tolerance studies were conducted under laboratory conditions for coccons ofAllorhogas pyralophagus Marsh, a Mexican parasitoid of graminaceous borers. By storage, developmental time (from cocoon to adult emergence) could be extended by 2 to 6 times. However, cocoons stored for more than 14 days at 2°C failed to survive, while at 5 and 10°C, about 50% emergence was recorded for upto 21 days of storage. With respect to survival and adult longevity, 10°C seemed to be the most suitable storage temperature. Pre-emergence period was also significantly increased by storing cocoons for 21 to 35 days at this temperature. Sex-ratio of emerging adults was not significantly affected by storage. Fecundity was adversely affected in all the treatments except in the case of females emerging from cocoons stored at 5°C for 7 days. The progeny of parasitoids which emerged from cocoons stored at 5 and 10°C for 35 days consisted of only males. It is clear from the present study thatA. pyralophagus cocoons are more amenable to short-term storage. Contribution No. 285/87 of the Indian Institute of Horticultural Research, Bangalore-560 089.  相似文献   

5.
Summary Mortality of neonatal pine beauty moth larvae varied from 0% to 100% depending on the duration of food deprivation and temperature. At 20°C and 100% RH all larvae had died by the fourth day of food deprivation, whereas at 10°C and 100% RH larvae survived for twelve days without food. Although larvae were able to survive at 15°C for up to seven days without food, establishment on thier host at this temperature was seriously affected by three days of starvation. No establishment took place after four days of starvation at 15°C. At 10°C establishment was significantly affected by starvation but not to such a marked degree. Establishment at both 15°C and 10°C was enhanced if the larvae were presented with a highly suitable host. The mean relative growth rate of those larvae reaching fifth instar was unaffected by the duration of their prefeeding starvation period. However, overall mean relative growth rates of the larvae were significantly affected by the duration of the starvation period. The implications of these results are discussed in relation to the population dynamics of this insect.  相似文献   

6.
Studies were carried out to investigate the effects of 5°, 10°, 15°, 20°, 25°, 30°, 35°, 40° and 45°C on growth, sexual maturity, reproduction and survival of the freshwater planorbid snail, Gyraulus convexiusculus, vector of echinostomiasis, under laboratory conditions. The growth rate of juvenile and sexually mature snails was at minimum at 15°C and was maximum at 35°C. Sexual maturation time was minimum at 35°C and maximum at 20°C. Fecundity was minimum at 15°C and maximum at 35°C. The minimum average and maximum number of eggs per egg capsule was reached at 35°C and lowest at 15°C. 30°C was the optimum temperature for survival of juvenile snails, while sexually mature snails reached maximum survival time at 20°C.  相似文献   

7.
Experiments were performed to determine suitable conditions for low temperature preservation of small S (Fukuoka) and ultra-small SS (Thai) strains of B. rotundiformis. For this, single rotifers (an adult bearing one egg or a 4-h neonate) were incubated for 10 days in 1 ml seawater (22 ppt salinity). The highest survival was achieved at 10 and 12 °C for S-strain and 12 °C for SS-strain. The effect of salinity, change of culture medium and feeding regime were further tested on rotifers (300 ind. ml–1) cultured in vials containing 10 ml seawater and microalgae at 12 °C. Survival of S-strain was highest (55.5±0.8%) at 35 ppt, while SS-strain survived best (43.1±2.6%) at 17 ppt. Survival was suppressed by changing the culture medium every 4 days. Feeding rotifers every 2 days yielded better survival (66.2±6.6%: S-strains, cultured at 35 ppt and 81.8±5.2%, SS-strains cultured at 17 ppt) than feeding them only at the beginning of the experiment or at 4-day intervals. An acclimation at 20 °C for 24 h before transferring them from their usual culture temperature (28 °C) to 12 °C resulted in higher survival of SS-strain. For S-strain, however, no significant improvement resulted from acclimation. SS-strain was more susceptible to lower temperature and higher salinity than S-strain.  相似文献   

8.
The effect of temperature on the ovipositional biology ofBoophilus annulatus (Say) was determined under laboratory conditions. Engorged females subjected to constant temperatures of 12 and 45°C died without ovipositing, while females held at 15 and 40°C laid eggs which did not hatch. The preoviposition period at 25–40°C was 2–3 days; however, significant increases occurred at 20°C (5.2 days) and at 15°C (16.3 days). The number of eggs laid per female was ca. 2700 at temperatures of 25–35°C, but decreased significantly at 20°C (ca. 2300 eggs/female), 15°C (ca. 1800 eggs/female), and at 40°C (ca. 300 eggs/female). No differences were observed in the Conversion Efficiency Index (CEI) values at temperatures of 20–30°C (ca. 50%), while temperatures of 15 and 40°C produced the lowest CEI values at 35.6 and 4.9%, respectively. Hatch-ability of eggs was ca. 80% at temperatures of 20–35°C. Incubation period of eggs ranged from 52.2 days at 20°C to 16.2 days at 35°C. The thermal threshold for egg development determined by linear regression was 12.9°C. Females subjected to four fluctuating temperature regimes produced no differences in number of eggs/female (ca. 2400), CEI (ca. 50%), or hatchability of eggs (ca. 75%). Preoviposition period and incubation were significantly affected by a change in the thermoperiod, becoming longer in duration as the temperatures were decreased. From studying females exposed for various intervals from 0 to 105 days at 12°C, indications were that the longer the exposure period the more adverse the effects were on oviposition and egg-hatch. Correspondingly, exposure of eggs to a temperature of 15°C for up to 105 days gave indications that the longer the eggs remained at 15°C, the lower the hatch would be after transfer back to a temperature of 25°C.  相似文献   

9.
Life table characteristics of Hypoaspis miles Berlese (Acarina: Hypoaspidae) fed on a mixture of Bradysia paupera Tuomikoski (Diptera: Sciaridae) and B. tritici Coquillet larvae were investigated in laboratory experiments at 4 temperatures (15, 20, 25, 30 °C) for development time, juvenile mortality, sex ratio, preoviposition period, oviposition period, postoviposition period, age-specific fecundity, and adult longevity. Juvenile development time decreased with increasing temperature from 46 days at 15 °C to 10 days at 30 °C. The lower temperature threshold was 9.9 °C and development required 205 °D. Juvenile mortality decreased from 52% at 15 °C to 3% at 25 °C and then increased to 24% at 30 °C. Preoviposition period varied with temperature from 12 days at 15 °C to 3 days at 25 °C and then increased to about 4 days at 30 °C. Oviposition period decreased with increasing temperature from 58 days at 15 °C to 25 days at 30 °C. The mean number of eggs per female per day increased from 0.4 at 15 °C to 2.3 at 25 °C and decreased to 1.3 at 30 °C. Age-specific fecundity was described by a temperature dependent model from which the maximum daily fecundity rate could be estimated to be attained at 25.6 °C. Female longevity was significantly shorter than for males, and decreased from 90 days at 15 °C to 34 days at 30 °C. Sex ratio was female-biased at all 4 temperatures and increased with temperature up to 25 °C, decreasing at 30 °C. Estimates of net reproductive rate, intrinsic rate of increase, finite rate of increase, mean generation time and doubling time were obtained. The r m -value increased with temperature from 0.031 day-1 at 15 °C to 0.133 day-1 at 25 °C, after which it decreased to 0.112 day-1 at 30 °C. The study showed that H. miles can develop and reproduce at temperatures between 15 and 30 °C. H. miles and sciarids have approximately the same optimum temperature and thresholds for development and reproduction and H. miles can be used for biological control of sciarids within the temperature range where the pest occurs.  相似文献   

10.
In 1991 and 1992, the Latin American epidemic strain of Vibrio cholerae O1 was isolated from ballast water, bilge water, and sewage taken from cargo ships docked in Mobile Bay, Alabama. The findings raised questions regarding the organism's ability to survive long-term aboard ships and to withstand the exchange of ballast at sea. The effects of temperature (6, 18, and 30°C) and salinity (8, 16, and 32 ppt) on survival of V. cholerae O1 strains C6706 and C6707 and a ballast water isolate in sterile seawater were determined. The ballast water isolate, which had a D-value (number of days required to produce a 1 log10 reduction in colony-forming units per milliliter) of 240 days at 18°C, 32 ppt salinity, had the longest survival time. The range of D-values was 36–240 days at 18°C, 60–120 days at 30°C, and 5–20 days at 6°C. In sterile seawater short-term survival was temperature dependent, whereas long-term survival was salinity dependent. In raw seawater, survival time of the ballast water isolate was reduced to 12–27 days, implying the existence of biological influences. As also shown in our previous work, the organism appeared to be able to survive for several months under relatively stable conditions in ballast water aboard ships; however, viability may be reduced to only a few weeks after the organism is introduced into estuarine or marine environments. Correspondence to: Susan A. McCarthy.  相似文献   

11.
Development, survival, reproduction and population growth statistics of apterous virginoparae of woolly apple aphid, Eriosoma lanigerum (Hausmann) (Hemiptera: Aphididae) at constant temperatures of 10, 13, 15, 20, 25, 30 and 32°C are reported. The developmental times of all life stages were inversely related to temperature ranging from 10 to 30°C. Span of total development (time from birth to adulthood) decreased from 57.8 days at 10°C to 11.7 days at 30°C and increased to 16.8 days at 32°C. A good linear model fit (R2>0.96) between developmental rate and temperature in the range 10–25°C was observed for all life stages. The lower developmental threshold was estimated at 5.8°C for instar I, 4.8°C for instar II, 4.9° for instar III and 4.4°C for instar IV. The lower temperature threshold for total development was estimated at 5.2°C. The upper developmental limit was found to be 32°C. Mean degree-day accumulations required for completion of instars I, II, III, IV and total development were: 125.6, 51.0, 47.7, 50.7 and 267.6, respectively. Fecundity, larviposition period and adult longevity were reduced with increasing temperature. Net reproductive rate was greatest at 15°C whereas intrinsic rate of increase peaked at 25°C. Optimal performance, as measured by fecundity, survival and intrinsic rate of increase, ocurred in the range 13–25°C.  相似文献   

12.
The development and survival of female Neoceratitis cyanescens (Bezzi) (Diptera: Tephritidae) from egg to complete ovarian maturation were studied in the laboratory at five different constant temperatures: 15, 20, 25, 30, and 35 °C. The aim of this study was to get information on the influence of temperature on pre-mature stages, as a prerequisite to optimise rearing procedures and to understand temporal and geographical patterns of fruit fly occurrence. The developmental rate of the different life stages increased linearly with increasing temperatures up to 30 °C. The fastest development of pre-mature stages was recorded at 30 °C (22±1 days) and the slowest at 15 °C (98±3 days). The day-degrees requirements (K) to complete total development were 432.6 day-degrees. Lower temperature thresholds were 11.4, 11.9, 10.0, and 11.1 °C for egg, larval, pupal stages and ovarian maturation, respectively. The number of adults obtained from an initial batch of 100 eggs reached a maximum (64) at 25 °C. At 35 °C, no adults emerged. Larval developmental time was significantly shorter in green tomato fruits than in potato tubers at 15, 20, and 25 °C. Mortality rate of larvae was higher in green tomato fruits than in potato tubers at 25 and 30 °C.  相似文献   

13.
Synopsis Growth and survival of Colorado squawfish, Ptychocheilus lucius, larvae under fluctuating 18, 22, and 26° C (5° C diel fluctuations) and constant 18, 22, 26° C, and 30° C temperature conditions and ration size corresponding to 12.5, 28,64,142, 320 brine shrimp nauplii fish–1 day–1 determined from laboratory experiments. Growth was optimal at 31° C and high at temperatures of 26° C to 30° C, at the highest food abundance. Lowest growth was under lowest food rations and highest temperatures. Growth of Colorado squawfish larvae declined substantially at temperatures < 22° C. Neither growth nor survival was significantly different between fluctuating or constant regimes. Survival of Colorado squawfish larvae was highest (95%) at 26.2° C and 235 nauplii fish–1 day–1 and high at temperatures of 20 to 30° C with food abundance > 180 nauplii fish–1 day–1. Survival was lowest when food abundance was low and temperature was high. Highest mortality occurred more than 20 days after experiments began and mortalities occurred sooner in higher than lower temperatures. Colorado squawfish larvae denied food for 5, 10, or 15 d after first feeding could have begun (6 d), had survival greater than 87 % which was equivalent to continuously fed controls. Survival of fish denied food for 17.5 d after feeding could have begun declined from 84% before feeding to 57% after feeding. Point of no return was estimated between 17.5 and 20 d. Colorado squawfish have relatively high starvation resistance. Low, stable flows that simulate natural hydrographs may enhance growth, survival, and recruitment of early life stages of Colorado squawfish by increasing water temperature and food abundance in regulated rivers of the Colorado River basin.  相似文献   

14.
The sycamore lace bug, Corythucha ciliata is a new, invasive pest of Platanus trees in China. Although C. ciliata is often subjected to acute low temperatures in early winter and spring in northern and eastern China, the cold tolerance of C. ciliata has not been well studied. The objectives of this study were to determine whether adults of C. ciliata are capable of rapid cold hardening (RCH), and to compare the benefits of RCH vs. cold acclimation (ACC) in the laboratory. When the adult females incubated at 26 °C were transferred directly to the discriminating temperature (−12 °C) for 2 h, survival was only 22%. However, exposure to 0 °C for 4 h before transfer to −12 °C for 2 h induced RCH, i.e., increased survival to 68%. RCH could also be induced by gradual cooling of the insects at rates between 0.1 and 0.25 °C min−1. The protection against cold shock obtained through RCH at 0 °C for 4 h was lost within 1 h if the adults were returned to 26 °C before exposure to −12 °C. Survival at both −12 and −5 °C was greater for RCH-treated than for ACC-treated adults (for ACC, adults were kept at 15 °C for 5 days), and the lethal temperature (2 h exposure) was lower for RCH-treated than for ACC-treated adults. The results suggest that RCH may help C. ciliata survive the acute low temperatures that often occur in early winter and early spring in northern and eastern China.  相似文献   

15.
The ability of the sweet potato whitefly, Bemisia tabaci Gennad., to survive a range of environmental conditions was investigated in the laboratory. The range of temperature and humidity investigated corresponds to the normal climatic range during B. tabaci's summer migration in Israel. Adult whiteflies confined to small test cages were exposed to combinations of temperature (25, 30, 35, and 41 °C) and relative humidity (20, 50, 80, and 100%) for periods of 2, 4, or 6 h.A logistic regression model describing the four-dimensional surface defining percent survival as a function of time, temperature, and humidity was developed. Using stepwise regression to exclude non-significant terms, the linear predictor included temperature, and the products of temperature and time, and humidity and time. The model accounted for 75% of the variance. A reparameterization of the fitted regression model suggests that survival potential is conditioned by temperature conditions prevailing during the previous 10 h.Whitefly survival after 2 h exposure ranged from 90% survival at 20°C and 100% RH, to <2% survival at 41°C and 20% r.h.. No whiteflies survived more than 2 h exposure at these latter extremes of temperature and humidity. Survival rates decreased slightly after experimental whiteflies were kept in a cage with food a further 20 h at 25±2°C, 55±5% r.h. Investigations of the effects of hunger and virus infection, showed that both increased mortality.  相似文献   

16.
Developmental rates for Copidosoma koehleri Blanchard (Hymenoptera: Encyrtidae) and its host, Phthorimaea operculella (Zeller), were determined at 10, 15, 23, 27, 29, 32, 34 and 35°C from host egg to adult. The developmental rates determined for both species showed good fit to mathematical models of insect development. At 15°C mean emergence of adult C. koehleri was 15 days after P. operculella adults emerged. At 29°C mean emergence of C. koehleri was only 5 days after that of P. operculella. P. operculella developed at 35°C, but parasitized larvae, and therefore C. koehleri, did not tolerate temperatures above 32°C. In the presence of C. koehleri, host survival was low (3%) at low host egg densities, but greater (20%) at higher host densities. Parasitized larvae of P. operculella were less able to compete for food resources, as measured by adult emergence.  相似文献   

17.
Summary Developoment, growth, and survival of larvae and pupae of the red turnip beetle, Entomoscelis americana Brown, were studied in 10 constant and four alternating temperature regimes (10 to 32.5° C), in field-cages, and in natural populations in Manitoba. This beetle has a northtemperate distribution in North America. Larval and pupal development occurs in spring and normally is completed before the end of June. Growth and development occurred at all constant temperatures tested, but survival was low at the extreme temperatures. Therefore, the threshold and upper limit were near 10 and 32.5° C. The developmental times of the sexes did not differ and decreased with temperature, except possibly at 32.5° C. The average weight of adult females increased with temperature up to 32.5° C and those of males up to 25° C. Considering developmental rate, survival, adult weight, and incidence of malformed adults, the optimum temperature was estimated to be near 27.5° C.Development was accelerated significantly (6 to 9%) in alternating regimes with temperatures differing by 10° C, but not in regimes differing by 5 and 15° C. All alternating regimes increased adult weight, 5 to 17% for females and 2 to 10% for males. Field cage studies confirmed the increase in adult weight, but not the acceleration in development.A three-parameter normal function described accurately the relationship between developmental rate and constant temperature. A computer simulation model based on this equation estimated developmental times in field cages to within one to five days. For natural populations the model overestimated the developmental times by five to 16 days. The discrepancies between model estimates and observed developmental times in natural populations apparently were due to the elevation of larval and pupal body temperatures above air temperatures by behavioral thermoregulation. The elevation of body temperature was estimated to be equivalent to the addition of 5 to 6° C to the maximum daily air temperature. The adaptations and responses of this beetle to the cool spring temperatures of the north-temperate region are discussed.Contribution No. 1164, Agriculture Canada, Research Station, Winnipeg, Manitoba, Canada  相似文献   

18.
Anthers of wheat cultivars Orofen and Pitic 62 were incubated for 8 days at 15, 20, 25, 30, 35 and 40°C before transfer to 25°C. Compared with anthers cultured at 25°C constantly, anthers treated at 30°C produced 40% more microspore callus and green plants in both cultivars whereas those treated at 35°C produced 2–3 fold more green plants. Treatment at 40°C was deleterious. Possible modes of action of high temperature on callus production and albinism were discussed.  相似文献   

19.
Previous reports on early-induced protein-calorie malnutrition (PCM) in rats have indicated alterations in the concentration of free amino acids and of protein synthesis in the brain. Recently it was shown that early-induced protein deprivation (PD) retards the development of thermoregulation. This resulted in a failure to maintain a normal rectal temperature after short exposure to room temperature (+22°C) still at the age of 20–25 days corresponding to changes seen in normal rats at an age of 10–15 days. In the present study, 20-day old PD and normal rats where examined with regard to the effect of exposure to room temperature on brain temperature and on brain free amino acids. The results show a similar reduction in brain and rectal temperature of the PD rats occuring within 30 minutes after exposure to room temperature. The reduction was in the range of 5°C. PD rats kept in room temperature for 5 hours and then allowed to recover at 32.5°C showed a slow increase in brain and rectal temperature but normal temperatures were not reached even after 1 hour. The concentration of free amino acids in the brain was examined in rats kept for 1 hour at room temperature or at 32.5°C. In the PD rats kept at 32.5°C, free aspartate and glutamate were reduced whereas taurine, GABA and glycine were increased as compared to their corresponding control rats. As a result of the reduced brain temperature in PD rats exposed to room temperature there was a reduction in free asparagine. The lability of the pool of asparagine may be related to the low levels of aspartate and glutamate in PD rats. On the basis of the present findings it is recommended that temperature-sensitive parameters are examined in PCM rats at a normal body temperature.Special Issue dedicated to Prof. Holger Hydén  相似文献   

20.
Cold tolerance in Tardigrada from Dronning Maud Land,Antarctica   总被引:1,自引:1,他引:0  
Survival at low temperatures was studied in three species of Tardigrada from Müihlig-Hofmannfjella, Dronning Maud Land, Antarctica. Both hydrated and dehydrated specimens of Echiniscus jenningsi, Macrobiotus furciger and Diphascon chilenense had high survival rates following exposure to -22°C for ca. 600 days, and dehydrated specimens following 3040 days at this temperature. In hydrated E. jenningsi, mortality increased with the duration of exposure from 7 to 150 days at -80°C, while mortalities of the two other species did not change. Hydrated specimens of all species were rapidly killed at -180°C, but all species exhibited good survivorship in the dehydrated state after 14 days at -180°C. In conclusion, hydrated tardigrades are able to survive extended periods at low temperatures, and dehydrated specimens are even better adapted to survive overwintering on Antarctic nunataks.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号