Embryogenesis and Postinfection Development of Meloidogyne konaensis

The effects of temperature on embryogenesis and postinfection development in Meloidogyne konaensis were examined. Embryogenesis was evaluated at 5, 8, 10, 13, 16, 20, 22, 24, 26, 28, 30, 35, and 40 C. No embryonic development occurred at 5 C. Some development, although incomplete, occurred at 8 and 10 C. The rate of embryogenesis was linear from 13 to 30 C, but decreased at 35 C. The lowest egg mortality occurred at 24 C, whereas all eggs died within 24 hours at 40 C. Postinfection development was determined on coffee and tomato in a greenhouse at an average temperature of 30 C and in a growth chamber with a constant temperature of 26 C. Development of M. konaensis J2 to mature female required 38 and 48 days on coffee at 30 and 26 C, respectively. This process took 20 and 26 days, respectively, on tomato.     

Temperature Effects on Development and Reproduction of Heterodera cajani on Pigeonpea

Effects of constant and fluctuating temperature on development and reproduction of Heterodera cajani were studied on pigeonpea cv. ICPL 87 in growth chambers at 10, 15, 20, 25, and 30 C and in a greenhouse fluctuating between 22.2 and 37.8 C. Nematode penetration was greatest (P = 0.001) in roots at 25 C; there was no penetration at 10 C. The basal threshold temperature for development was calculated to be 11 C. Completion of one H. cajani generation required 17, 28, 35, and 66 days (323, 392, 315, and 264 degree-days) at 30, 25, 20, and 15 C, respectively, and 19 days (356 degree-days) at a fluctuating temperature. Survival was greater at 20 and 25 C than at 15 and 30 C. The greatest (P = 0.05) number of females (17.9 females per root) were produced at 25 C, compared with 13.2 at 20 C, 7.9 at 30 C, and 2.5 females at 15 C. Nematode reproduction was 1.6 to 7.1 times greater at 25 C than at other temperatures. Emergence of juveniles from egg sacs and cysts was greater at 25 and 30 C than at 15 and 20 C. Equations were developed to predict nematode development rate, cumulative juvenile emergence from egg sacs and cysts, and population increases as influenced by temperature.     

Temperature-dependent development and life table parameters of Octodonta nipae (Coleoptera: Chrysomelidae)

The effect of temperature on the development, survivorship, fecundity, and life table parameters of Octodonta nipae (Maulik) (Coleoptera: Chrysomelidae), was studied at seven constant temperatures of 17.5, 20, 22.5, 25, 27.5, 30, and 32.5°C. Preliminary experiments showed that no development was observed at 15 and 35°C. All individuals completed development and females laid eggs from 20 to 30°C. There was a significant decrease in male and female longevity with increasing temperatures from 20 to 30°C. The longest and shortest longevity were 203.5 and 73.7 d for males, and 178.7 and 57.6 d for females, respectively. Females produced on average 62.7, 88.9, 116.8, 70.0, and 47.3 eggs and the life expectancy for a newborn egg was 171.6, 148.7, 114.9, 89.2, and 94.8 d at 20, 22.5, 25, 27.5 and 30°C, respectively. Life history data were analyzed by using an age-stage, two-sex life table. The intrinsic rate of increase (r) and the finite rate of increase (λ) of O. nipae increased with increasing temperatures from 20 to 30°C, while the mean generation time (T) decreased within this temperature range. The r was 0.0155, 0.0249, 0.0339, 0.0361, and 0.0383 d(-1) at 20, 22.5, 25, 27.5, and 30°C, respectively. The net reproductive rate (r(0)) was highest at 25°C (35.0 offspring), and lowest at 20°C (17.0 offspring). T was shortest at 30°C (76.4 d). The results showed that temperature greatly affected the fecundity and life table parameters of O. nipae, and a suitable temperature for population development and fecundity was at 25°C. The life table data can be used for the projection of population growth and evaluation of control programs.     

Effect of Temperature on Attachment,Development, and Interactions of Pasteuria penetrans on Meloidogyne incognita

The effect of temperature (10, 20, 25, 30, and 35 C) on attachment and development of Pasteuria penetrans on Meloidogyne arenaria race 1 was elevated in growth chambers. The greatest attachment rate of endospores of P. penetrans occurred on second-stage juveniles at 30 C. The bacterium developed more quickly within its host at 30 and 35 C than at 25 C or below. The development of the bacterium within the nematode female was divided into nine recognizable life stages, which ranged from early vegetative thalli to mature sporangia. Mature sporangium was the predominant life stage observed after 35, 40, 81, and 116 days at 35, 30, 25, and 20 C, respectively. The body width and length of M. arenaria females infected with P. penetrans were smaller initially than the same dimensions in uninfected females, but became considerably larger over time at 25, 30, and 35 C. This isolate of P. penetrans also parasitized and completed its life cycle in males of M. arenaria.     

Population Response to Temperature in the Subfamily Tylenchorhynchinae

The effects of temperature on population development of 11 species of stunt nematodes in the subfamily Tylenchorhynchinae were compared on red clover or Kentucky bluegrass in constant-temperature tanks at 5-degree intervals from 10 to 35 C. The optimum temperature for population increase on red clover in 90 days was 30 C for Tylenchorhynchus agri, T. nudus, T. martini, and T. clarus, 25 C for T. sylvaticus and T. dubius, and 20 C for T. canalis, Merlinius brevidens, and Quinisulcius capitatus. The optimum was 30 C for T. robustoides and 25 C for T. maximus on Kentucky bluegrass. The temperature range for population increase was 20-35 C for T. agri, T. nudus, T. martini, and T. clarus, 20-30 C for T. sylvaticus and T. robustoides, 15-25 C for T. maximus, 10-25 C for T. dubius, and 10-20 C for M. brevidens and Q. capitatus. T. canalis increased only at 20 C. All species were recovered in numbers near their inoculum level at 10 C. There was no survival of T. sylvaticus, T. dubius, T. canalis, T. robustoides, T. maximus, M. brevidens, and Q. capitatus at 35 C, or of the last three of these species at 30 C. Temperature had no effect on sex ratio in final populations. Population increase was greatest in T. martini and least in T. canalis.     

Effects of temperature on Anoplophora glabripennis (Coleoptera: Cerambycidae) larvae and pupae

Developmental thresholds, degree-days for development, larval weights, and head capsule widths for each larval instar and the pupal stage of Anoplophora glabripennis (Motschulsky) (Coleoptera: Cerambycidae) were studied at eight constant temperatures (5, 10, 15, 20, 25, 30, 35, and 40°C) for two source populations (Ravenswood, Chicago, IL [IL], and Bayside, Queens, NY [NY]). The estimated lower threshold temperature for development of instars 1-5 and the pupal stage was near 10°C and was near 12°C for the higher instars. Developmental rate was less temperature sensitive for instars 5-9 compared with instars 1-4. Development for all but the first instar was inhibited at constant temperatures >30°C, and all instars failed to develop at 40°C. Although the two source populations had similar responses to temperature, IL larvae were heavier than those from NY. Temperature and its influence on larval weight had profound impacts on whether a larva proceeded to pupation. Based on the temperature effects detailed here, larval development and pupation should be possible in most of the continental United States where suitable hosts are available. These data can be used to develop a degree-day model to estimate beetle phenology; however, at least 2°C should be added to air temperatures to adjust for the mediation of temperature by the wood. These data provide a basis for predicting the potential geographical range of this species and for developing phenological models to predict the timing of immature stages, both of which are important for management programs.     

Effect of Time,Temperature, and Inoculum Density on Reproduction of Pratylenchus thornei in Carrot Disk Cultures

Reproduction of Pratylenchus thornei on carrot disk cultures at different time periods after inoculation, temperature, and initial inoculum density was studied. At 25 C and with an initial inoculum of 25 females per disk, the final nematode population increased with increasing time after inoculation, although the populations after 25 and 50 days were not different. Nematode numbers increased by 1,255-fold and 3,619-fold at 75 and 100 days, respectively. Over 35 days incubation at 15, 20, 25, and 30 C, the nematode multiplied 1.8, 8.4, 10.5, and 0.4 times, respectively. The optimum temperature for reproduction was between 20 and 25 C, and the nematode life cycle was completed in about 25-35 days. Increasing nematode inoculum (25, 50, 100, 500, 1,000 nematodes per disk) increased the final nematode population but did not increase reproduction rate, the highest being 25.3 at an initial inoculum density of 100 nematodes per disk.     

Effects of temperature and diet on development and interspecies competition in Aedes aegypti and Aedes albopictus

We asked whether climate change might affect the geographic distributions of Aedes aegypti (L.) and Aedes albopictus (Skuse) (Diptera: Culicidae). We tested the effects of temperature, diet and the presence of congeneric species on the performance of immature stages of these two aedine species in the laboratory. Mosquitoes in three different species-density combinations were reared at four constant temperatures (20 °C, 25 °C, 30 °C, 35 °C) on low- or high-level diets. Of the four temperatures tested, mortality increased only at 35 °C in both species. Mortality was higher on the high-level diet than on the low-level diet at 35 °C, but not at other temperatures. The presence of congeneric species had a significant positive effect on mortality in Ae. albopictus, but not in Ae. aegypti. Both species developed more quickly at higher temperatures within the range of 20-30 °C; development was not enhanced at 35 °C. Population growth of Ae. albopictus was more stable, regardless of diet and temperature; that of Ae. aegypti varied more according to these two factors. These species-specific attributes may help to explain the latitudinal distribution of the mosquitoes and degree of species dominance where they are sympatric.     

Temperature-dependent development of Chilocorus bipustulatus (Coleoptera: Coccinellidae)

The effect of temperature on development and survival of Chilocorus bipustulatus L. (Coleoptera: Coccinellidae), a predator of many scale insects, was studied under laboratory conditions. The duration of development of egg, first, second, third, and fourth larval instars, pupa, and preovioposition period at seven constant temperatures (15, 17.5, 20, 25, 30, 32.5, and 35°C) was measured. Development time decreased significantly with increasing temperature within the range 15-30°C. Survival was higher at medium temperatures (17.5-30(ο)C) in comparison with that at more extreme temperature regimens (15 and >30(ο)C). Egg and first larval instars were the stages where C. bipustulatus suffered the highest mortality levels at all temperatures. The highest survival was recorded when experimental individuals were older than the third larval instar. Thermal requirements of development (developmental thresholds, thermal constant, optimum temperature) of C. bipustulatus were estimated with application of linear and one nonlinear models (Logan I). Upper and lower developmental thresholds ranged between 35.2-37.9 and 11.1-13.0°C, respectively. The optimum temperature for development (where maximum rate of development occurs) was estimated at between 33.6 and 34.7°C. The thermal constant for total development was estimated 474.7 degree-days.     

Temperature effects on immune response and hematological parameters of channel catfish Ictalurus punctatus vaccinated with live theronts of Ichthyophthirius multifiliis

This study evaluated the influence of temperature on the immune responses and hematological parameters in channel catfish Ictalurus punctatus immunized via intraperitoneal injection with live theronts of Ichthyophthirius multifiliis. Fish were distributed in 18 aquaria and received 9 treatments: 4 groups of fish were vaccinated with live theronts and maintained at constant temperature 15 °C, 20 °C, 25 °C and 30 °C; 3 groups of fish vaccinated and subjected to cycling temperature regime from 15-25 °C, 20-25 °C and 20-30 °C, changed 5 °C each day; 2 groups of fish were not vaccinated and served as controls at 25 °C, one with Ich challenge and the other without challenge. Non vaccinated fish and those vaccinated at 15 °C or 15-25 °C did not show anti-Ich antibodies in the serum 14 and 21 days post-immunization. The antibody levels were significantly higher from fish vaccinated at 25 °C, 30 °C, 20-25 °C and 20-30 °C compared to fish at 15 °C, 20 °C and 15-25 °C both 14 and 21 days post-immunization. At constant water temperature, fish vaccinated at 15 °C showed significantly higher mortality rate (67.8%, P < 0.05) than those vaccinated at 20 °C, 25 °C, and 30 °C (0-10.7% mortalities). At cycling water temperature, fish vaccinated at 15-25 °C showed significantly higher mortality rate (67.8%) than those vaccinated at 20-25 °C and 20-30 °C (P < 0.05). Twenty days after immunization fish vaccinated at 30 °C and 20-30 °C showed significant increase in the red blood cells, white blood cells, thrombocytes and monocytes. Six days after challenge with I. multifiliis theronts the fish showed decreased white blood cells, thrombocytes and monocytes. This study suggests that vaccinated catfish were severely impacted by low temperature, either at 15 °C constant temperature or at 15-25 °C cycling temperature. The fish showed no anti-Ich antibodies and suffered high mortality similar to non vaccinated control fish.     

Influence of Temperature on Embryogenesis in Meloidogyne javanica

The optimum temperature for embryogenesis in Meloidogyne javanica lies between 25 and 30 C. Embryogenesis is slightly more rapid at 30 C (9-10 days), but more eggs complete development at 25 C (11-13 days). At temperatures of 25, 27.5, and 30 C, embryogenesis is about twice as rapid as at 20 C (23-25 days), and about four times as rapid as at 15 C (46-48 days). Time-lapse studies showed that the thermal optimum is similar throughout the different stages of embryonic development.     

Development of Heterodera glycines Life Stages as Influenced by Temperature

The effects of temperature on rates of development of Heterodera glycines egg and juvenile stages were examined as a basis for predicting generation times of the nematode on soybean. The relationship of temperature to H. glycines embryonic development between 15 and 30 C was described by a linear model, The calculated basal temperature threshold was 5 C. Thermal optimum for embryogenesis and hatch with low mortality was 24 C. Development proceeded to first-stage juvenile at 10 C and to second-stage juvenile at 15-30 C. Hatch occurred at 20-30 C. At 36 C, development proceeded to the four-cell stage, then the eggs died. The range of diurnal soil temperature fluctuation and accumulated degree-days between 5 and 30 C (DD5/30) had an impact on rate of development of juveniles in soybean roots. From early June to early July, H. glycines required 534 + 24 DD5/30 (4 weeks) to complete a life cycle in the field. During the midseason (July and August), life cycles were completed in 3 weeks and 429 ± 24 DD5/30 were accumulated. Late in the season (September to November), declining soil temperatures were associated with generation times of 4 weeks and slower rates of development.     

Temperature-related development and population parameters for Typhlodromus pyri (Acari: Phytoseiidae) found in Oregon vineyards

The beneficial mite Typhlodromus pyri is a key predator of grapevine rust mite Calepitrimerus vitis in Pacific coastal vineyards. Rust mite feeding has been associated with damage such as stunted, deformed shoot growth and reductions in fruit yield. The life history traits of T. pyri were assessed at seven constant temperatures (12.5, 15, 17.5, 20, 25, 30 and 35 °C) to determine population parameters providing data to better predict biological control of C. vitis populations by T. pyri in vineyards. Successful development from the egg to adult stage was observed at temperatures ranging from 15 to 30 °C. Constant exposure to 12.5 and 35 °C resulted in 100 % mortality in immature T. pyri. Developmental times, fecundity and longevity were highest at 25 °C. The estimated minimum and maximum developmental thresholds were 7.24 and 42.56 °C, respectively. Intrinsic rate of increase (r ( m )) was positive from 15 to 30 °C indicating population growth within this range of temperatures. Net reproductive rate and intrinsic rate of increase were greatest at 25 °C. These developmental parameters can be used to estimate population growth, determine seasonal phenology and aid in conservation management of T. pyri. Results presented in this study will aid in evaluating the effectiveness of T. pyri as a key biological control agent of C. vitis during different periods of the growing season in Pacific Northwest vineyards.     

Comparison of temperature and moisture requirements for sporulation of Aspergillus flavus sclerotia on natural and artificial substrates

A key step in the infection cycle by Aspergillus flavus in maize is sporulation of sclerotia present in soil or in crop debris. However, little information is available on this critical and important phase. This study included experiments on artificial (Czapek Dox Agar (CZ)) and natural (maize stalks) substrates under different conditions of temperature (T; from 5 to 45 °C) and water activity (a(w); from 0.50 to 0.99) levels to quantify sporulation from sclerotia. The mean numbers of spores were higher on defined nutritional medium in vitro on CZ agar than on maize stalks (4.5×10(6) spores/sclerotium versus 4.2×10(4) spores/sclerotium) with production initiated after 6 and 24h, respectively. Surprisingly, the optimal temperature was found at 30-35 °C for CZ agar (9.23×10(6) spores/sclerotium) and to be 20-25 °C for maize stalks (6.26×10(4) spores/sclerotium). Water stress imposition only reduced sporulation at ≤0.90 a(w.) With more available water no significant differences were found between 0.90 and 0.99 a(w). This type of data is critical in the development of a mechanistic model to predict the infection cycle of A. flavus in maize in relation to meteorological conditions.     

Temperature dependence of cardiac sarcoplasmic reticulum Ca²⁺-ATPase from rainbow trout Oncorhynchus mykiss

In this work, the temperature dependence of the sarco-endoplasmic reticulum Ca(2+) -ATPase (SERCA2) activity from rainbow trout Oncorhynchus mykiss cardiac ventricles was measured and compared with the mammalian SERCA2 isoform. The rate of ATP-dependent Ca(2+) transport catalysed by O. mykiss vesicles was totally abolished by thapsigargin and the Ca(2+) ionophore A(23187) . At warm temperatures (25 and 30° C), the SERCA2 from O. mykiss ventricles displayed the same rate of Ca(2+) uptake. At 35° C, the activity of the O. mykiss enzyme decreased after 20 min of reaction time. The rate of Ca(2+) uptake catalysed by the mammalian SERCA2 was temperature dependent exhibiting its maximal activity at 35° C. In contrast to the rate of Ca(2+) uptake, the rate of ATP hydrolysis catalysed by O. mykiss SERCA2 was not significantly different at 25 and 35° C, but the rate of ATP hydrolysis catalysed by the rat Rattus norvegicus SERCA2 isoform at 35° C was two-fold higher than at 25° C. At low temperatures (5 to 20° C), the rate of Ca(2+) uptake from O. mykiss SR was less temperature dependent than the R. norvegicus isoform, being able to sustain a high activity even at 5° C. The mean ±s.e. Q(10) values calculated from 25 to 35° C for ATP hydrolysis were 1·112 ± 0·026 (n = 3) and 2·759 ± 0·240 (n = 5) for O. mykiss and R. norvegicus, respectively. Taken together, the results show that the O. mykiss SERCA2 was not temperature dependent over the 10 to 25° C temperature interval commonly experienced by the animal in vivo. The Q(10) value of SERCA2 was significantly lower in O. mykiss than R. norvegicus which may be key for cardiac function over the wide environmental temperatures experienced in this eurythermal fish.     

Temperature effects on the immature development time of Culex eduardoi Casal & García (Diptera: Culicidae)

The effect of constant temperatures on the development time from first instar to adult emergence was studied in Culex eduardoi Casal & García reared at 7, 10, 15, 20, 25, 30 or 33°C. Data were adjusted to the linear degree-day model and the nonlinear Briére model. According to the linear model, the development time was inversely related to the rearing temperatures between 7°C and 25°C. Maximum mortality (100%) was recorded at temperatures > 30°C. According to the linear model, the development threshold temperature and thermal constant were 5.7°C and 188.8 degree days, respectively. The lower and upper threshold temperatures and the optimum temperature for the nonlinear model were -2.3, 30.0 and 28.1°C, respectively.     

Importance of Temperature in the Pathology of Meloidogyne hapla and M. chitwoodi on Legumes

Effects of temperatures on the host-parasite relationships were studied for three legume species and four populations of root-knot nematodes from the western United States. The nematode populations were Meloidogyne hapla from California (MHCA), Utah (MHUT), and Wyoming (MHWY), and a population of M. chitwoodi from Utah (MCUT). The legumes were milkvetch (Astragalus cicer), alfalfa (Medicago sativa), and yellow sweet clover (Melilotus officinalis). All milkvetch plants survived inoculation with all nematode populations, while alfalfa and yellow sweet clover were more susceptible. On yellow sweet clover, MHCA was most pathogenic at 30 °C based on suppression of shoot growth while MHUT, MHWY, and MCUT were most pathogenic at 25 °C. All nematode populations suppressed growth of yellow sweet clover more than growth of milkvetch and alfalfa. The reproductive factor (Rf = final nematode population/initial nematode population) of MHCA was positively correlated (r = 0.83) with temperature between 15 °C and 30 °C. The greatest Rf occurred on alfalfa inoculated with MHCA at 30 °C. The Rf of MHUT, MHWY, and MCUT were positively correlated (r= 0.76, r= 0.78, and r= 0.73, respectively) with temperature between 15 °C and 25 °C. The Rf values of MHUT and MHWY were similar on all species and exceeded the Rf of MCUT at all temperatures (P < 0.05).     

Pathological Reaction of Crested Wheatgrass Cultivars to Four Meloidogyne chitwoodi Populations

Meloidogyne chitwoodi populations from Tulelake, California; Ft. Hall, Idaho; Beryl, Utah; and Prosser, Washington, significantly (P < 0.05) reduced dry shoot weights of crested wheatgrass (Agropyron cristatum L., Gaertn. and A. desertorum, Fisch. ex Link, Schult.) cultivars Hycrest, Fairway, and Nordan in experiments conducted in a greenhouse and growth chamber. Shoot growth depression, root galling, and nematode reproduction indices were greatest (P < 0.05) on plants inoculated with 5,000 eggs/plant. Nematode populations from Tulelake, Ft. Hall, and Beryl significantly (P < 0.05) reduced the growth of the three grass cultivars at 15, 20, 25, and 30 C; the greatest reductions occurred at 20 and 25 C. There were significant differences in the virulence of the nematode populations at high (30 C) and low (15 C) soil temperatures. At 15 C, plant growth was reduced more by the Beryl and Tulelake than by the Ft. Hall population; whereas at 30 C, the Ft. Hall population was more virulent than the Beryl and Tulelake populations. Root galling and nematode reproduction were greater on plants inoculated with Beryl and Tulelake populations at 15 C than on plants inoculated with the Ft. Hall population, while the Ft. Hall population had the most pronounced effects at 30 C.     

Effect of temperature on pupa development and sexual maturity of laboratory Anastrepha obliqua adults

The effect of four temperatures (18, 20, 25 and 30°C) on pupa development and sexual maturity of Anastrepha obliqua adults was investigated under laboratory conditions. The results showed that the duration of the pupal stage decreased with an increase in temperature (29, 25, 13 and 12 days, respectively), and maintaining the pupae at 18°C and 20°C results in a low percentage of pupation, pupa weight loss and lesser flying ability. However, it significantly favored sexual behavior, a higher proportion of sexual calls and matings. While enhanced pupa development was observed at a temperature of 30°C, adults had low sexual efficiency, as well as a lower proportion of calls and matings. Gas chromatography-mass spectrometry (GC-MS) analysis of male volatiles showed that the amount of (Z,E)-α-farnesene did not vary among males from pupae reared at different temperatures; however, less (E,E)-α-farnesene was emitted by males obtain from pupa reared at 30°C. Male flies kept at 30°C during their larval stage had more (Z)-3-nonenol and, also, an unknown compound was detected. The fecundity of the females was higher at low temperatures. Regarding fertility, no significant differences were found between temperatures. The optimal temperature on pupa development was 25°C when males displayed ideal attributes for rearing purposes.     

Lowering storage temperature during ovary transport is beneficial to the developmental competence of bovine oocytes used for somatic cell nuclear transfer

The objective of this study was to determine the effect of storage temperature during ovary transport on the developmental competence of bovine oocytes for use in somatic cell nuclear transfer (SCNT). Ovaries obtained from a slaughterhouse were stored in physiological saline for 3-4h at one of the three temperatures: 15 °C, 25 °C, or 35 °C. The developmental competence of oocytes used for SCNT was ascertained by cleavage and blastocyst formation rate, total cell number, apoptosis index, and the relative abundance of Bax and Hsp70.1 in day 7 blastocysts. Ovaries stored at 35 °C for 3-4h reduced the recovery rate of grade I and II oocytes compared with those stored at 25 °C or 15 °C (45.1±0.7% vs. 76.7±1.2% or 74.8±2.0%, P<0.05). The proportion of oocytes matured to the MII stage (maturation rate) for oocytes stored at 35 °C was significantly lower than those stored at 25 °C or 15 °C (51.3±0.9% vs. 75.1±1.4% or 71.7±1.3%, P<0.05). Cleavage rate (77.7±2.1%, 77.9±1.1% and 72.1±0.7% for 15 °C, 25 °C and 35 °C groups, respectively) and blastocyst formation rate (39.1±0.5%, 36.8±1.4% and 32.2±0.9% for 15 °C, 25 °C and 35 °C groups, respectively) following SCNT were not significantly different between treatments. Oocytes from ovaries stored at 15 °C, however, produced blastocysts with higher cell numbers (97.3±8.6 vs. 80.2±10.8 or 77.4±11.7; P<0.05) and lower apoptotic index (5.1±1.3 vs. 13.5±1.6 or 18.6±1.1, P<0.05) than those stored at 25 °C or 35 °C. The relative abundance of Bax and Hsp70.1 in day 7 blastocysts produced from oocytes derived from ovaries stored at 15 °C was lower than those stored at 25 °C or 35 °C (P<0.05). It was concluded that a storage temperature of 15 °C for a 3-4h period had a significant beneficial effect on the quality and developmental competence of oocytes used for SCNT due to the alleviation of stresses on the oocytes compared with those subjected to storage temperatures of 25 °C or 35 °C.